CC BY-NC-ND 4.0 · Geburtshilfe Frauenheilkd 2018; 78(12): 1262-1282
DOI: 10.1055/a-0713-1058
GebFra Science
Review/Übersicht
Georg Thieme Verlag KG Stuttgart · New York

Diet and Lifestyle Before and During Pregnancy – Practical Recommendations of the Germany-wide Healthy Start – Young Family Network

Article in several languages: English | deutsch
Berthold Koletzko
1   Kinderklinik und Kinderpoliklinik, Dr. von Haunersches Kinderspital, LMU – Ludwig-Maximilians-Universität, München, Germany
2   Deutsche Gesellschaft für Kinder- und Jugendheilkunde e. V. (DGKJ), Berlin, Germany
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
,
Monika Cremer
4   Netzwerk Gesund ins Leben/Bundeszentrum für Ernährung (BZfE) in der Bundesanstalt für Landwirtschaft und Ernährung (BLE), Bonn, Germany
,
Maria Flothkötter
4   Netzwerk Gesund ins Leben/Bundeszentrum für Ernährung (BZfE) in der Bundesanstalt für Landwirtschaft und Ernährung (BLE), Bonn, Germany
,
Christine Graf
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
5   Deutsche Sporthochschule Köln, Köln, Germany
,
Hans Hauner
6   Lehrstuhl für Ernährungsmedizin, Klinikum rechts der Isar der Technischen Universität München, München, Germany
,
Claudia Hellmers
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
7   Hochschule Osnabrück, Osnabrück, Germany
8   Deutsche Gesellschaft für Hebammenwissenschaft e. V. (DGHWi), Münster, Germany
,
Mathilde Kersting
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
9   Forschungsdepartment Kinderernährung, Klinik für Kinder- und Jugendmedizin, Universitätsklinikum der Ruhr-Universität Bochum, Bochum, Germany
,
Michael Krawinkel
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
10   Institut für Ernährungswissenschaft, Justus-Liebig-Universität Gießen, Gießen, Germany
11   Deutsche Gesellschaft für Ernährung e. V. (DGE), Bonn, Germany
,
Hildegard Przyrembel
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
,
Marianne Röbl-Mathieu
12   Mitglied der Ständigen Impfkommission am Robert Koch-Institut (STIKO), Berlin, Germany
,
Ulrich Schiffner
13   Poliklinik für Zahnerhaltung und Präventive Zahnheilkunde, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany
14   Deutsche Gesellschaft für Kinderzahnheilkunde e. V. (DGKiZ), Würzburg, Germany
,
Klaus Vetter
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
15   Nationale Stillkommission, Bundesinstitut für Risikobewertung (BfR), Berlin, Germany
,
Anke Weißenborn
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
16   Bundesinstitut für Risikobewertung (BfR), Berlin, Germany
,
Achim Wöckel
3   Mitglied im wissenschaftlichen Beirat des Netzwerks Gesund ins Leben, Bonn, Germany
17   Frauenklinik und Poliklinik Universitätsklinikum Würzburg, Würzburg, Germany
› Author Affiliations
Further Information

Correspondence/Korrespondenzadresse

Prof. Dr. Berthold Koletzko
LMU – Ludwig-Maximilians-Universität München
Dr. von Haunersches Kinderspital
Lindwurmstr. 4
80337 München
Germany   

 

Maria Flothkötter
Netzwerk Gesund ins Leben im Bundeszentrum für Ernährung (BZfE) in der Bundesanstalt für Landwirtschaft und Ernährung (BLE)
Deichmanns Aue 29
53179 Bonn
Germany   

Publication History

received 01 August 2018
revised 22 August 2018

accepted 22 August 2018

Publication Date:
25 September 2018 (online)

 

Abstract

Diet and exercise before and during pregnancy affect the course of the pregnancy, the childʼs development and the short- and long-term health of mother and child. The Healthy Start – Young Family Network has updated the recommendations on nutrition in pregnancy that first appeared in 2012 and supplemented them with recommendations on a preconception lifestyle. The recommendations address body weight before conception, weight gain in pregnancy, energy and nutritional requirements and diet (including a vegetarian/vegan diet), the supplements folic acid/folate, iodine, iron and docosahexaenoic acid (DHA), protection against food-borne illnesses, physical activity before and during pregnancy, alcohol, smoking, caffeinated drinks, oral and dental hygiene and the use of medicinal products. Preparation for breast-feeding is recommended already during pregnancy. Vaccination recommendations for women planning a pregnancy are also included. These practical recommendations of the Germany-wide Healthy Start – Young Family Network are intended to assist all professional groups that counsel women and couples wishing to have children and during pregnancy with uniform, scientifically-based and practical information.


#

Introduction

The first 1000 days post conception are regarded as a sensitive window of time that can define the childʼs health and in which the risk of later non-transmissible diseases can be modified [1]. The importance of a healthy lifestyle with a balanced diet and exercise in this phase of life is an important building block for the prevention of these diseases and is underlined by, amongst others, the national health goal “Before and after birth” of 2017 [2].

In Germany, about a third of women of childbearing age are overweight or obese [5]. Obesity reduces the likelihood of conception [6] and is associated, amongst others, with a higher risk of pregnancy and birth complications, birth defects, premature births and miscarriages, a high infant birth weight and later obesity of the child [6], [7]. In 2014/15 gestational diabetes was diagnosed in 13% of pregnant women during a screening programme [8]. About 11% of mothers of 0- to 6-year-old children reported in the German Health Interview and Examination Survey for Children and Adolescents (KiGGS) that they had smoked during pregnancy [11]. It is estimated that about 0.2 – 8 out of 1000 neonates in Germany are born annually with fetal alcohol syndrome. Far more children are affected by a fetal alcohol spectrum disorder [12].

A healthy lifestyle prevents risks of pregnancy complications and helps maintain the health of mother and child. In this phase of life in particular expectant parents[ 1 ] are often highly motivated to optimise their lifestyle and are receptive to appropriate recommendations. Women and couples wishing to have children are less aware that their lifestyle affects fertility, the course of the pregnancy and also the childʼs later health.

The recommendations of the Healthy Start – Young Family Network (Netzwerk Gesund ins Leben) are intended to help contribute to a health-promoting lifestyle and thus to promote the health of mothers and children and prevent long-term overweight and its associated diseases. In 2012 the Germany-wide Practical Recommendations for Nutrition in Pregnancy of the Healthy Start – Young Family Network were first published [13]. The updated version presented here has been extended to include recommendations covering the period before pregnancy and around the time of conception.

They are intended to provide gynaecologists, midwives, paediatricians and members of other health professions with a basis for counselling a healthy lifestyle.

Healthy Start – Young Family is a network of institutions, learned societies and associations that are concerned with young families. The aim is to provide parents with uniform messages about nutrition and exercise so that they and their children live healthy lives and grow up healthy.

The Healthy Start – Young Family Network is part of the IN FORM initiative and is accommodated in the Federal Centre for Nutrition (BZfE), an institution that comes within the sphere of responsibility of the Federal Ministry of Food and Agriculture (BMEL).


#

Methods

For the update of the recommendations on nutrition in pregnancy [13] and the extension to include recommendations for women wishing to have children, in 2017 the recommendations of national and international learned organisations and institutions were searched for statements on the diet, exercise, lifestyle and health of pregnant women and those wishing to have children and examined for their topicality.

In addition, literature searches were undertaken in PubMed, Cochrane Library and Google Scholar[ 2 ] and meta-analyses, systematic reviews, guidelines and relevant publications published between 2012 and mid-2017 were assessed by the members of the scientific council (cf. list of authors). In addition, aspects of lifestyle before conception, physical activity before and during pregnancy and weight recommendations for pregnancy were discussed in working groups with other acknowledged experts and practitioners (see page 1274) from the appropriate specialist disciplines. On this basis, the present recommendations were formulated by consensus by the scientific council. A more wide-ranging systematic literature search and evidence assessment was not undertaken because of the lack of financial resources for this. The key statements formulated correspond to the evidence level of an expert recommendation with particular regard to aggregated sources of evidence. Their wording is based on that used in guidelines. Thus, “must” refers to a strong recommendation (German “soll”), “should” to a moderately strong recommendation (German “sollte”) and “can” to an open recommendation (German “kann”). The respective “Bases of the recommendations” sections make it apparent how these were derived.

These practical recommendations have been reviewed and endorsed by the boards of the following associations: Professional Association of German Gynaecologists (BVF), the German Association of Midwives (DHV), the Professional Association of Paediatricians (BVKJ); and the following scientific societies: German Society of Pediatrics and Adolescent Medicine), German Society of Obstetrics and Gynaecology (DGGG), German Society for Sport Medicine and Prevention (DGSP), German Society of Midwifery Science (DGHWi) and German Society for Nutrition (DGE).


#

General Recommendation

Recommendation
  • Professional groups who care for women of childbearing age, particularly women with a concrete wish to have children, as well as pregnant women must encourage and counsel them to follow a balanced diet, physical activity and a healthy lifestyle.

Women/couples wishing to have children and expectant parents are frequently unaware that they can exert a long-term effect not only on their own health but also on that of their children through their nutrition and their lifestyle [3], [4], [14]. The lifestyle of a future family is influenced by both partners. Professionals must inform women of childbearing age and their partners, women/couples wishing to have children and expectant parents of the long-term importance of a healthy lifestyle and know that a third of pregnancies are unplanned or are not planned for that particular time [15].


#

Body Weight Before Conception and Weight Gain in Pregnancy

Recommendations
  • Even before pregnancy, the optimal adjustment of body weight to a normal weight is desirable.

  • An appropriate weight gain in pregnancy is between about 10 and 16 kg for women of normal weight.

  • In the case of overweight and obese women, a lower weight gain in pregnancy is desirable.

  • In underweight women, it should be ensured that there is sufficient weight gain during pregnancy.

Bases of the recommendations

Meta-analyses and systematic reviews underline the fact that both women who are overweight and those who are underweight before conception have a higher health risk than those with normal weight [16], [17], [18], [19], [20]. The recommendation that women should adjust their body weight before pregnancy to that approaching a more normal weight is consistent with international [4] and national recommendations [21], [22].

A weight gain of between 10 and 16 kg is associated with a low risk of fetal and maternal complications in women of normal weight [25], [26], [27]. The risk increases with a higher weight gain [28], particularly if the woman is overweight or obese when embarking on pregnancy [29]. Therefore a weight gain of about 10 kg is regarded as sufficient for overweight and obese women. A general recommendation for a minimum weight gain in underweight women cannot be given. Overall, the evidence is too inconsistent to define exact upper and lower limits for a desirable weight gain in pregnancy according to preconceptual body mass index (BMI). Internationally there is no consensus on the recommendations for weight gain in pregnancy, particularly for overweight and obese women [30], [31].


#

Background information

In Germany, 30% of 18- to 29-year-old women, 38% of 30- to 39-year-olds and 46% of 40- to 49-year-olds are overweight or obese (DEGS1) [5]. Only up to about 4.5% of women in these age groups are underweight [5]. Overweight/obesity before pregnancy and also high weight gain in pregnancy (frequently defined as weight gain above the recommendation of the Institute of Medicine [IOM], see below) were associated in observational studies with an increased occurrence of gestational diabetes, hypertension and birth complications [16], [18], [19], fetal macrosomia [20], large for gestational age (LGA) and later overweight of the child and associated complications [19], [32], [33], [34]. Maternal overweight and obesity at the beginning of pregnancy are associated with a shorter life expectancy of the child [35]. Underweight in pregnancy was associated with more frequent premature births, miscarriages and low birth weight [17], [36], [37], [38]. It is therefore desirable for both overweight and underweight women to approximate to normal weight before pregnancy. Weight gain in pregnancy is characterised by high variability [23], [24] and has a lower predictive significance than BMI at the beginning of pregnancy.

For women who are obese, even a weight loss of 5 to 10% of the starting weight before pregnancy can have a significantly positive effect on health and also increase the chance of becoming pregnant [22]. The therapeutic measures (if necessary including bariatric surgery) that may be considered for weight reduction in severely obese women in preparation for a pregnancy must be decided individually in a medical consultation on the basis of current scientific findings and guidelines [39], [40], [41].

Pronounced weight gain normally does not occur until the second trimester of pregnancy. Pregnant women should be informed of the causes of weight gain and the risks of obesity or excessive weight gain. Weight loss diets in pregnancy are not recommended because of safety concerns.

The American Institute of Medicine (IOM) [27] recommends a different weight gain for pregnant women according to BMI at the beginning of pregnancy [27]. These recommendations are based on epidemiological association studies in American and Danish women. The recommendations have been adopted by some countries such as Italy, Denmark and Switzerland, in some cases with slight adjustments. As the weight ranges recommended by the IOM could not be confirmed in other international [42] and national epidemiological studies [24], [43] and could not be substantiated by the results of a few interventional studies on a change of lifestyle in normal and overweight/obese women [44], [45], [46], [47], their use in everyday clinical practice is not recommended here and by other expert groups [13], [22] (cf. also Suppl. Table S1).

The increased risk of later overweight in the child as a result of a high maternal weight gain in pregnancy is also discussed, but the weight gain during pregnancy has less effect on the risk of overweight and the childʼs health than the baseline weight of the mother in particular [48], [49], [50].


#
#

Energy and Nutritional Requirements in Pregnancy

Recommendations
  • Pregnant women should pay particular attention to the quality of their diet. Compared to the energy requirement, the requirement for individual vitamins and minerals/trace elements increases much more in pregnancy.

  • Energy requirements increase only slightly over the course of pregnancy. Pregnant women should increase their energy intake only slightly (up to about 10%) and not until the last few months of pregnancy.

Basis of the recommendations

The recommendations take account of the mathematically determined increase in energy requirements, which is the basis of international and national reference values [4], [25], [51], [52], and the usually markedly reduced physical activity, particularly in the third trimester [53].


#

Background information

A high-calorie diet can have a detrimental effect on the course of pregnancy and on the childʼs health [54], [55], [56], [57]. Pregnant women often overestimate their actual increase in energy requirement. Energy consumption increases in particular due to the energy requirement for tissue formation and fetal growth. Purely mathematically, there is an additional energy requirement of 76 530 kcal for a woman of normal weight and a weight gain in pregnancy of 12 kg [58]. From this is derived the guideline value of the German Nutrition Society (DGE) for an additional energy intake of 250 kg kcal/day in the second trimester and 500 kcal/day in the third trimester with unchanged physical activity [52]. However, physical activity usually declines considerably [59], [60], so that in many women an increased energy intake is not required.

The requirement for a series of vitamins and minerals increases in pregnancy much more than the energy requirement, mainly from the 4th month onwards [61]. For the nutrients folate and iodine a markedly increased intake is recommended from the beginning or even before pregnancy [52]. Recommended additional intake of various nutrients are indicated in [Fig. 1]. With the exception of folate and iodine [52] (see section Supplements), the increased requirement for vitamins and minerals can usually be covered by a suitable choice of food. The consumption of supplements cannot replace a balanced diet. During counselling the concept of “think for two but do not eat for two (do not eat double portions)” should be emphasised and illustrated by examples of foods with high nutrient densities (vegetables, fruit, wholegrain products, dairy products, etc.).

Zoom Image
Fig. 1 Reference nutrient values – Recommended additional intake in pregnancy according to German Nutrition Society (DGE), expressed as a percentage of the reference value [52].

#
#

Nutrition

Recommendations
  • The diet must be balanced and varied before and during pregnancy. It should be based on the general recommendations for healthy adults.

  • In a balanced diet, the food groups should be weighted differently:

    • Both calorie-free beverages and plant-based foods (vegetables, fruit, pulses, wholegrain products) should be consumed abundantly.

    • Animal-based foods (milk and dairy products, low-fat meat and low-fat meat products, oily sea fish and eggs) should be eaten moderately.

    • Sweets, sugar-containing beverages and snacks as well as fats with a high proportion of saturated fatty acids (in particular animal fats) and oils should be only consumed sparingly. Plant oils (e.g. rapeseed and olive oil) should be preferred as sources of fat.

Bases of the recommendations

International [4], [19] and national [52], [62] learned societies and institutions give recommendations for a balanced and varied diet before and during pregnancy that are based on the general recommendations for adults [52], [63]. The data are insufficient to allow special nutritional recommendations to be formulated, e.g. for improving fertility [64]. There is no robust evidence for particular diets or for preferring certain macronutrients (proteins, carbohydrates, fats) for weight loss or for the avoidance of excessive weight gain in pregnancy [57], [65].


#

Background information

A balanced diet and regular physical activity before and during pregnancy not only have a positive short-term effect on the course of pregnancy and the development of the unborn child, but also have positive long-term effects on the health and well-being of mother and child [1], [4], [66]. A systematic review showed that weight gain and the risk of pre-eclampsia can be reduced by diet and lifestyle interventions in pregnancy (in normal-weight, overweight and obese women), in addition to which a non-significant trend to reduction of gestational diabetes, hypertension, premature births and intrauterine death was observed [67]. In an interventional study in overweight pregnant women with an increased risk of gestational diabetes, appropriate weight gain and a lesser decline in physical activity in early pregnancy was achieved through repeated healthy eating and physical activity messages [68]. No reduction in gestational diabetes was obtained with other lifestyle interventions in obese pregnant women [65]. Although the data are inconsistent, nutrition and exercise should be addressed repeatedly when counselling pregnant women.

In a meta-analysis of 11 randomised interventional studies (1985 pregnant women, mean BMI 21.5 – 32.4 kg/m2), a diet with a low glycaemic index was associated with lower blood glucose concentrations in the women (fasting and 2 hours postprandially) and a lower risk of large for gestational age (LGA) infants than a diet with a higher glycaemic index [69]. A systematic review of observational studies showed a lower risk of gestational diabetes with a diet with a high intake of vegetables, fruit, wholegrain products, nuts, pulses and fish; by contrast, a diet rich in fat, a large amount of red meat and eggs was associated with a higher risk [9].

Because of the physiological changes and the growth of the uterus (the stomach and intestine are compressed), smaller meals divided over the day can promote the well-being of the expectant mother.

With a balanced diet, the food groups can be divided according to the recommended frequencies and amounts of consumption into “abundant”, “moderate” and “sparing”. Foods with a high nutrient density (high content of essential nutrients relative to their energy content) are required for sufficient amounts of vitamins and minerals to be absorbed despite the only slight increase in energy requirement. With the nutrients folate and iodine, the increased requirement could theoretically be covered by a very specific choice of food [70], although in practice this is rarely achieved (see section “Supplements”).

A guideline value for the daily amount of water for the general population and also during pregnancy is about 1.5 L [52]. In hot environments or during heavy physical activity, a larger amount of water is required.

The daily consumption of at least three portions of vegetables and two portions of fruit is desirable [63]. Cereal products, particularly from wholegrain cereals, and potatoes are rich in vitamins, minerals and fibre. Milk and dairy products, which provide protein, calcium and iodine, are important components of a balanced diet. Fish is an important source of vitamin B12, zinc and iron. A preference for certain types of meat is not necessary for an adequate iron intake, but low-fat meat and meat products should be chosen specifically.

Through the weekly consumption of fish, particularly one portion of oily sea fish (e.g. mackerel, herring or sardines), it is possible to achieve the additionally recommended quantity of the long-chain omega-3 fatty acid docosahexaenoic acid (DHA) of at least 200 mg/day in pregnancy (for fish/DHA in relation to allergy prevention, see section “Nutrition for the prevention of allergies in the child”). A high consumption of carnivorous fish (e.g. tuna, swordfish), which are at the end of the maritime food chain and may contain a high content of toxic substances, should be avoided for reasons of preventive health care in pregnancy [52], [71]. The regular consumption of sea fish as well as iodised salt contributes to the supply of iodine. However, salt should be used sparingly.


#
#

Vegetarian and Vegan Diet in Pregnancy

Recommendations
  • A balanced vegetarian diet with the consumption of milk, dairy products and eggs (ovo-lacto vegetarianism) can in principle cover most nutrient needs even during pregnancy. Specific counselling is recommended.

  • In the case of a purely plant-based (vegan) diet, the supply of critical nutrients must be checked by a physician and individual nutritional counselling given. As well as iodine and folic acid, additional micronutrient supplementation (particularly vitamin B12) is required to prevent a nutrient deficiency and subsequent damage to the childʼs development.

Bases of the recommendations

The study data on vegetarian and vegan diets in pregnancy is sparse and in some cases contradictory [72]. The recommendations are therefore based on the general recommendations for an ovo-lacto vegetarian diet with due regard to the “critical” nutrients in pregnancy [62], [73]. An undersupply of vitamin B12 occurring after many years of a vegan diet without supplementation can lead to severe and long-lasting damage to the childʼs nervous system as well as haematological and neurological problems for the mother during pregnancy [74], [75], [76].


#

Background information

Sufficient nutrient intake is possible in pregnancy with a balanced and consciously designed ovo-lacto vegetarian diet, with the exception of the nutrients folic acid and iodine (and in some cases DHA), which generally need to be supplemented during pregnancy.

Milk and dairy products, eggs, pulses and cereal products usually provide sufficient protein intake. The risk of insufficient iron intake is increased for ovo-lacto vegetarians [77], [78]. Pulses, (wholegrain) cereal products and some types of vegetable contain reasonably large quantities of iron, although less readily available than iron from meat and fish. The concomitant consumption of vitamin C-rich foods (e.g. citrus fruits, peppers) can improve iron intake. Depending on the medically determined iron status, iron may be supplemented if necessary (see section “Supplements”). Critical nutrients for pregnant women following a vegetarian diet for a long time even before they became pregnant include vitamin B12, DHA and possibly zinc [74], [77], [79], [80].

With a purely plant-based (vegan) diet, intake of vitamin B12, DHA, zinc, protein, iron, calcium and iodine is critical. In particular, adequate intake of vitamin B12 is not possible with a purely plant-based diet without nutritional supplements and fortified foods. Vegans who wish to keep to their diet in pregnancy should undergo qualified nutritional counselling as soon as they wish to have children in order to eliminate any nutritional deficiencies before conception. Vegans should have their intake of critical nutrients regularly checked medically during pregnancy as well, so that they can take specific supplements and where necessary consume fortified foods to cover their nutrient requirement [73].


#
#

Supplements

Folic acid supplement

Recommendations
  • In addition to a balanced diet, women planning a pregnancy must take 400 µg of folic acid daily or equivalent doses of other folates in the form of a supplement.

  • Supplementation must begin at least four weeks before conception and continue until the end of the first trimester of pregnancy.

  • Women who start folic acid supplementation less than 4 weeks before conception should use higher-dosed products.

Bases of the recommendations

It has been found in numerous epidemiological studies and meta-analyses based on these studies that periconceptual folic acid supplementation of 400 µg/day (alone or in combination with other micronutrients) can reduce the risk of birth defects of the nervous system (neural tube defects; NTD) (e.g. [81], [82], [83], [84], [85], [86]). In Germany and many other countries it has therefore been recommended since about the middle of the 1990s that, in addition to a folate-rich diet, women who want to or could become pregnant should take 400 µg of folic acid daily or equivalent doses of other folates (calcium L-methylfolate or 5-methyltetrahydrofolic acid glucosamine) in the form of supplements and continue the supplementation also in the first trimester of pregnancy [87], [88], [89], [90]. In some countries the dose recommendation is somewhat higher, e.g. 500 µg daily in Australia [91]. If intake begins only shortly before or even after conception, supplements of 800 µg folic acid should be used [92], [93] in order to reach the red blood cell folate concentrations recommended by the WHO more rapidly [94].


#

Background information

Folate is important for cell division and growth processes, amongst others. Consumption of folate-rich plant nutrients such as greens, cabbages, pulses, wholegrain products, tomatoes or oranges can contribute to the supply of folate. According to the German National Nutrition Survey (NVS II), the median intake of folate equivalents in women of reproductive age is between 153 and 185 µg/day [95] and thus markedly below the German, Austrian and Swiss reference values for nutrient intake derived for adults (300 µg/day) and pregnant women (550 µg/day) [52]. In the German Health Interview and Examination Survey for Adults (DEGS1), serum and red blood cell folate concentrations were for the first time measured representatively for the adult population. The results of this study give rise to the conclusion that 85% of the population reaches the target folate values for non-pregnant women [96]. However, fewer than 5% of women of reproductive age reach the red blood cell folate concentration of 400 ng/mL (906 nmol/L) recommended by the WHO for effective risk reduction of neural tube defects [94], [96].

As closure of the neural tube normally occurs within 3 to 4 weeks of conception, folic acid supplementation must be started prior even to conception for the greatest possible risk reduction of neural tube defects. The time interval until the recommended folate concentration is reached is dependent on the baseline concentration and the supplemented dose: thus, with a daily intake of 400 µg of folic acid, 6 to 8 weeks are needed to reach a red blood cell folate concentration of 906 nmol/L; with an intake of 800 µg/day, however, only about 4 weeks are required [92], [93], [97]. A daily intake of 1000 µg folic acid/day is considered safe (tolerable upper intake level) [98], [99].

Currently only a small proportion of women in Germany take a preventive folic acid supplement. Admittedly almost 90% of women take a folic acid supplement in pregnancy [100], but only about 10 to 34% begin at the recommended time and use a dose of at least 400 µg/day [101], [102], [103]. In Germany, dosage forms in different doses are available. If women take a multivitamin product purely for NTD prevention, it should be ensured that this contains at least 400 µg of folic acid.


#
#

Iodine supplement

Recommendation
  • In addition to a balanced diet, pregnant women must take a daily supplement of 100 (up to 150) µg iodine. Women with thyroid disorders must consult their physician before supplementation.

Bases of the recommendation

According to WHO criteria [104], Germany is an area with a mild to moderate iodine deficiency. The median iodine intake in women of reproductive age (calculated from iodine excretion in the 24-hour urine) according to the DEGS study was about 125 µg/day [105]. Thus, the median value did not reach either the reference intake for adult women of 200 µg/day [52] or the higher recommended intake of the German Nutrition Society for pregnant women of 230 µg/day [52]. A supplement with a dose of 100 to 150 µg daily appears sufficient to achieve the recommended intake for pregnancy. The dose equates to the lower to middle end of the range for iodine supplementation in pregnancy mentioned in the maternity guidelines and regarded as safe (100 to 200 µg/day) [106]. It is comparable to the recommendations of international bodies [107], [108], [109].


#

Background information

Women wishing to have children should be counselled about the importance of iodine even before pregnancy. Consideration should be given to an adequate iodine intake. The use of iodised cooking salt and the regular consumption of milk, dairy products and sea fish are worth recommending (see also section “Nutrition”). In terms of foodstuffs (e.g. bread), products with iodised table salt should be chosen out of preference. Women with thyroid disorders should be given medical advice and also avoid iodine deficiency. In women with Hashimotoʼs thyroiditis, the required level of iodine intake (through iodised salt, foods with added iodised salt, fish, etc.) is usually unproblematic.

In pregnancy, the iodine requirement increases due to the increased maternal production of thyroid hormones and increased renal excretion, but also due to the requirement for the unborn childʼs development (placental transfer). In total, an increased iodine requirement of about 30 to 50 µg/day is assumed [52], [110]. Accordingly, the reference value derived by the German, Austrian and Swiss societies for iodine intake increases from 200 µg to 230 µg/day [52]. Based on an adequate intake value of 150 µg/day for non-pregnant women, the EFSA recommends an intake of 200 µg/day in pregnancy [110]. If products with 100 to 150 µg iodine are already being taken, additional iodine supplements should not be taken.

A series of epidemiological studies indicate that even a moderate undersupply of iodine, particularly in early pregnancy, or a deficiency of thyroid hormones (hypothyroxinaemia) during this period can have an unfavourable effect on the childʼs cognitive and psychomotor development [111], [112], [113], [114], [115], [116], [117]. The few studies in which the effects on pregnancy of iodine supplementation in moderate iodine deficiency have been investigated [114], [116], [118], [119], [120] indicate that the mother also benefits from iodine supplementation and has a lower risk of developing hypothyroidism after the birth.

The iodine content in sea algae, particularly in dried algae and seaweed products, can vary considerably and in some cases be very high. Thus, even with small dietary quantities of algae/products, as well as when taking several iodised nutritional supplements, there may be an increased iodine intake [121], [122]. In addition, algae can be rich in arsenic and other contaminants [122]. The consumption of algae and algal products is therefore discouraged.


#
#

Other supplements

Recommendations
  • Iron supplements in addition to a balanced diet should only be taken after a medically diagnosed deficiency.

  • Pregnant women who do not consume oily sea fish regularly are recommended to take DHA supplements.

Bases of the recommendations

Iron supplementation in pregnancy improves maternal status and protects against anaemia; however, as regards the benefit to the child of general supplementation of all pregnant women, the data are inconclusive [123], [124], [125]. In addition, there is evidence that additional iron intake in well-supplied pregnant women can increase the risk of premature births and low birth weight [126], [127]. Against this background, general prophylactic iron supplementation is not recommended for pregnant women in Germany. This is consistent with recommendations of other European countries (e.g. UK [128], France [129] and Ireland [130]. On the other hand, routine supplementation of iron in combination with folic acid is recommended internationally by the WHO in pregnancy since in some developing countries there is a considerable proportion of pregnant women who have iron deficiency anaemia [4], [19], [131].

The omega-3 fatty acid docosahexaenoic acid (DHA) is found in particular in oily sea fish. Pregnant women who abstain from these foods should take supplements with DHA to achieve the recommended intake amount in the German, Austrian and Swiss reference values of at least 200 mg DHA daily on average [52] or the additional intake recommended by the EFSA in pregnancy of 100 to 200 mg DHA, in addition to the recommended intake for non-pregnant women of 250 mg DHA daily plus eicosapentaenoic acid (EPA) [132], [133].


#

Background information

Iron deficiency in pregnancy increases the risk of premature birth and low birth weight [126], [134], [135]. The iron requirement increases in pregnancy because more iron is required for the fetus, placenta and the 20% increase in red blood cells in the expectant mother. Pregnant women should therefore ensure a sufficient intake of iron-rich foodstuffs.

The reference value for iron intake in pregnancy in Germany of 30 mg/day is 100% higher than that for non-pregnant women [52]. According to NVS II, women of childbearing age (18 to 49 years) consume a median of 11 to 12 mg iron per day [95]. These data indicate that the generally recommended intake amount in the normal diet is not reached. However, menstrual blood loss ceases [52] and intestinal iron absorption increases in pregnancy. Therefore, the EFSA, for example [136], assumes an equally high dietary iron requirement for pregnant women as for non-pregnant women. As well as determinations of Hb, the additional determination of serum ferritin [137] in the context of antenatal care is useful in obtaining evidence of insufficient or empty iron stores [106].

Vegetarians have a small intake of DHA and have a lower DHA status than women who also consume fish, meat and eggs [138]. The alpha-linoleic acid (ALA) contained in some vegetable oils (e.g. rapeseed, walnut, linseed oil), nuts and seeds (e.g. walnuts) can provide a contribution to the supply of omega-3 fatty acid; however, endogenous synthesis of DHA from ALA is low [138], [139], [140], [141], [142], [143], [144]. Women who do not (regularly) consume oily sea fish should therefore take DHA as a supplement during pregnancy.

In randomised controlled trials, supplementation with fish oil or long-chain omega-3 fatty acids such as DHA resulted in a significant reduction in the risk for early premature births up to 34 weeks of pregnancy [145], [146], [147]. DHA is important for the development of visual function and brain in the fetus [148]. In some observational studies, the consumption of fish and the supply of long-chain omega-3 fatty acids in pregnancy were associated with a more favourable childhood development of cognitive and other abilities [149], [150], [151], [152], [153]. Other studies fail to confirm this [154], [155]. Data on the benefit of DHA supplements in pregnancy for the childʼs cognitive development are inconsistent.

The vitamin D supplied to the expectant mother exerts an effect on fetal vitamin D supply and infant bone mineralisation [156], [157], [158]. Vitamin D is formed in particular in the skin during exposure to sunlight. Thus, a supply of vitamin D can be guaranteed by spending a regular amount of time outdoors. For light skin types, it is sufficient in the summer months in our latitudes to expose the unprotected face and arms to the sun for about 5 to 10 minutes daily in the midday period. Sunburn should be avoided at all costs. In the absence of endogenous vitamin D synthesis, i.e. in periods of low sunlight and with a predominantly indoor existence, the German Nutrition Society recommends a vitamin D intake of 20 µg (800 IU) daily for pregnant women (as for all other groups of people from infancy onwards) [52]. The average amount of vitamin D absorbed from the diet is only 2 to 4 µg daily [95]. This is insufficient to achieve a sufficient intake with limited exposure to sunlight and low endogenous vitamin D synthesis throughout the year. Pregnant women who rarely spend time in the sun or extensively cover their skin or use sunscreen lotions on exposure to the sun as well as women with dark skin types should therefore use a supplement with vitamin D [52].


#
#
#

Protection against Food-Borne Illnesses During Pregnancy

Recommendations
  • Pregnant women must avoid raw, animal-based foods. In addition, they should follow the recommendations to avoid listeriosis and toxoplasmosis in the choice, storage and preparation of foods.

  • Pregnant women must only eat eggs if the yolk and egg white are firm from being heated.

Bases of the recommendations

Recommendations on the choice, preparation and storage of foods are summarised in the information sheet published in 2017 “Listeriosis and toxoplasmosis. Safe eating during pregnancy” from the Federal Centre for Nutrition [161] (order no. 0346, www.ble-medienservice.de). They are based on data from zoonosis monitoring and other communications from the Federal States on the presence of zoonosis pathogens in foodstuffs studied and study results of food-related disease outbreaks, literature analyses and expert opinions as well as from members of the Committee for Biological Hazards and Hygiene at the Federal Institute for Risk Assessment. As salmonellosis can be harmful to mother and child, eggs should be consumed only when cooked thoroughly.


#

Background information

The pathogens of listeriosis and toxoplasmosis can be transmitted to the placenta and the unborn child during pregnancy and cause severe illnesses as well as premature births and stillbirths [159], [160]. Each year about 20 to 40 cases of neonatal listeriosis and about 5 to 40 cases of congenital toxoplasmosis in neonates [162], [163] are reported to the Robert Koch Institute (www.rki.de), but the reporting system only covers laboratory-confirmed cases. A national seroprevalence study estimates there to be 345 cases of congenital toxoplasmosis annually in Germany [164].

In the case of toxoplasmosis, the consumption of raw meat from pigs, lambs, sheep and game as well as of meat that is not fully cooked (including in the form of raw sausage meat such as salami or raw ham) is particularly problematical [160], [165], [166].

Raw meat products, smoked fish and soft cheeses (including those made from heat-treated milk such as Gorgonzola) have a high risk of containing pathogenic listeria; raw milk and derived products as well as vegetables and salads may also be affected [159], [167], [168], [169], [170]. Listeria can also be found in heated foods. It can also proliferate at refrigerator temperatures as well as in products packaged under vacuum or in a controlled atmosphere.

Pregnant women should prepare their food as close as possible to the time of consumption and consume it rapidly. In restaurants and cafeterias they should where possible consume food that has been heated immediately prior to consumption. As well as choice of foods, hygiene in storage and preparation plays an important role in protecting against food-borne illnesses.


#
#

Exercise Before and During Pregnancy

Recommendations
  • Women who are planning a pregnancy and pregnant women must follow the general exercise recommendations for adults.

  • Women must also be physically active in everyday life during pregnancy and must limit or regularly interrupt sedentary activities.

  • Pregnant women should be moderately physically active for at least 30 minutes at least 5 days a week and preferably daily. Moderately active means that conversation is still possible during sporting activity (talk test).

  • Women who engage in sport can also be more intensively physically active in pregnancy.

Bases of the recommendations

The recommendations are based on recommendations by other learned societies and expert groups such as the National Recommendations for Physical Activity and Physical Activity Promotion [53], [171], [172], [173], [174], [175].

Meta-analyses and systematic reviews of randomised controlled interventional studies as well as observational studies suggest that moderate physical activity during pregnancy is not only safe for the pregnant woman and the child [176], [177], but also produces a variety of positive effects. Thus exercise/sport during pregnancy is associated with a reduced risk of LGA [178], [179], premature birth [177], [180], [181], caesarean section [44], [176], [182], [183], gestational diabetes [10], [47], [176], [177], [178], [184], pregnancy-induced hypertension [176], [183], excessive weight gain [44], [178], [185], [186], incontinence [187], [188], back pain [189], [190] and improved psychosocial well-being [53]. Data findings focused exclusively on overweight and obese pregnant women are not quite so extensive. In summary, in this respect a risk reduction has been demonstrated for premature birth, gestational diabetes and excessive weight gain by the practice of physical activity as part of a lifestyle intervention in pregnancy [44], [177].


#

Background information

The recommendations on the level of activity of 30 minutes of physical activity on at least 5 days a week are documented by the improvement in cardiorespiratory and muscular fitness and the prevention of noncommunicable diseases [191]. In terms of pregnancy-specific aspects, the evidence for certain levels and intensities of activity is limited; generally, however, in a complication-free pregnancy the positive effect of exercise on the course of the pregnancy and the health of mother and child is undisputed [192].

For pregnant women, aerobic endurance activity is particularly recommended and should be undertaken at moderate intensity [193] and in exercise units of at least 10 minutes. Moderate intensity means the exercise is experienced as slightly strenuous and conversation is possible (talk test). Physical activity in everyday life is also desirable, e.g. walking quickly or climbing steps. The aim of 10 000 steps a day can serve as a guide for the level of daily activities [194], [195], which should be supplemented by sporting activities. Types of sports that draw upon large muscle groups are particularly suitable, including for beginners, and include walking, Nordic walking, bicycling at moderate speed, swimming/aqua fitness, cross-country skiing and low impact aerobic or pregnancy yoga. Women should not begin new types of sports with unaccustomed sequences of movement in pregnancy. Types of sports that are considered inappropriate are those with a high risk of falls and injury, e.g. team, contact or fighting sports or scuba-diving [53]. Healthy pregnant women can be physically active at elevations of up to 2000 to 2500 m, particularly if they are accustomed to these elevations [196], [197]. Women who engage in sport can continue their previous sporting activity in a complication-free pregnancy and train somewhat more intensively than beginners [171], [193], [198], [199].

Possible warning signs are vaginal bleeding, labour, loss of amniotic fluid, dyspnoea, dizziness, headache, chest pain, muscular imbalance, calf pain and swelling [53]. Physical activity is contraindicated in haemodynamically relevant heart diseases, restrictive lung disease, cervical insufficiency, premature labour, persistent bleeding in the second and third trimester, placenta praevia after 26 weeks of pregnancy, ruptured amniotic sac, pre-eclampsia, pregnancy-induced hypertension or severe anaemia [53].

In reality, the level of exercise frequently declines during pregnancy [53], [60]. Reported barriers are lack of time, lack of motivation and above all fears and safety aspects [200]. Professionals should encourage pregnant women to arrange their everyday life and leisure time so as to be active and to limit or regularly interrupt sedentary activities. They should take the concerns and anxieties of pregnant women/expectant parents seriously and inform them that exercise is desirable in a normal healthy pregnancy and safe for mother and child.


#
#

Alcohol

Recommendation
  • Women who are planning a pregnancy and pregnant women must avoid alcohol.

Bases of the recommendation

On the basis of the available evidence it is not possible to define a safe and risk-free amount of alcohol for the fetus or a time window in pregnancy when alcohol consumption does not present a risk [204]. National and international learned societies [4], [52], [205] and the Federal Centre for Health Education (BZgA) therefore advise against drinking alcohol during pregnancy. It is also recommended to refrain from alcohol during the period of planning a pregnancy [3], [4], [206], [207].


#

Background information

Alcohol consumption during pregnancy can lead to birth defects, growth restriction, damage to tissue and nerve cells as well as to an irreversible reduction in the childʼs intelligence and can exert an effect on its behaviour (hyperactivity, impulsivity, distraction, risky behaviour, infantilism and disorders of social maturity) [201], [202], [203]. Fetal alcohol syndrome (FAS) is the most common avoidable disability in neonates with an estimated incidence of 0.2 – 8 in 1000 neonates [12]. Substantially more children are affected by a fetal alcohol spectrum disorder [12], [203]. The extent of the individual health risk to the child is difficult to predict and is affected by maternal and fetal characteristics. Although large systematic studies have demonstrated no negative long-term effect of mild to moderate alcohol consumption [208], it is safest to avoid all alcohol consumption [209]. The recommendation “to avoid alcohol in pregnancy” could promote uncertainty or feelings of guilt in women who consumed alcohol early in pregnancy before they were aware of the pregnancy. For this reason, specialists should provide differentiated and sensitive advice.


#
#

Smoking

Recommendations
  • Women/couples who are planning a pregnancy should not smoke.

  • Pregnant women must avoid smoking and stay in rooms where people are smoking or have smoked.

Bases of the recommendations

The recommendation to change smoking habits even during the phase of wishing to have a child and of not smoking in pregnancy meet the recommendations of the Fédération Internationale de Gynécologie et dʼObstétrique (FIGO) [4], other national specialist organisations [62], [128] and the Federal Centre for Health Education [218].


#

Background information

Smoking has a negative effect on fertility [64] and can increase the risk for premature births and miscarriages, birth defects, premature placental detachment and low birth weight, but also the later risk for obesity and allergies in the child [210], [211], [212], [213], [214], [215], [216], [217]. In Germany, 26% of 18- to 25-year-old women and 34% of men of the same age smoke [11]; in older age groups, the proportion is somewhat higher (30% of women, 35% of men) [219]. Of the mothers of 0- to 6-year-old children questioned in the KiGGS study, 11% had smoked in pregnancy. Pregnant women under 25 years of age at the time of their childʼs birth or belonging to a low socioeconomic group had smoked twice as often during pregnancy as older women or women with a high socioeconomic status [220].

All professional groups who counsel women/couples wishing to have a child, pregnant women and expectant parents should discuss smoking and where necessary explicitly and repeatedly address the persons they are counselling about their cigarette consumption or their habits. They should motivate them to adopt weaning measures and point out that the wish to have children and pregnancy are good opportunities to stop smoking. To encourage smoking cessation, materials are also specifically available for pregnant women and for disseminators as well as advice lines (www.rauchfrei-info.de).

Nicotine is frequently contained in e-cigarettes. Even for e-cigarettes without nicotine, health concerns are raised [221]. Pregnant women are therefore recommended to avoid e-cigarettes.


#
#

Caffeinated Beverages During Pregnancy

Recommendation
  • Pregnant women should drink caffeinated beverages only in moderate amounts.

Bases of the recommendation

The data are inadequate for assessing possible detrimental effects of caffeine on the mother and child and for quantifying amounts of caffeine that do not present a risk. A dose-dependent association between caffeine consumption in pregnancy and the risk of fetal growth retardation and negative effects on birth weight has been observed in studies [222], [223]. The EFSA gives a safe caffeine dose for the period of pregnancy of 200 mg/day [224].


#

Background information

Caffeine crosses the placenta rapidly but cannot be metabolised either by the fetus or in the placenta [224]. The relationship between maternal caffeine intake and pregnancy duration, birth weight, fetal growth retardation and small for gestational age (SGA) has been investigated in studies. According to a current meta-analysis of case-control and observational studies, there is a significantly increased risk of spontaneous abortion from 300 mg caffeine daily and above [225]. Another meta-analysis shows a linear association between caffeine consumption and miscarriage rate, although other possible confounding factors were not considered [226]. A Cochrane meta-analysis was unable to draw any conclusions about the effectiveness of abstention from caffeine on birth weight or other relevant endpoints because of limited data [227].

Data on the mean caffeine content of beverages are shown in [Table 1]. Energy drinks must not contain more than 320 mg caffeine/litre [228] and those containing 150 mg caffeine per litre and over must be labelled “Increased caffeine content. Not recommended for children and pregnant or breast-feeding women” [229]. Further typical ingredients of energy drinks are glucuronolactone, taurine and inositol, the interactions between which have not been fully established, as well as large amounts of sugar. Pregnant women should therefore avoid energy drinks.

Table 1 Mean caffeine contents of drinks (according to EFSA 2015 [224] and BfR 2015 [230]).

200 ml filter coffee:

about 90 mg

60 ml espresso:

about 80 mg

200 ml black tea (1 cup):

about 45 mg

200 ml green tea (1 cup):

about 30 mg

250 ml cola drinks:

25 mg/330 ml (can about 35 mg)

250 ml energy drink (1 tin):

about 80 mg

200 ml cocoa drink:

8 to 35 mg


#
#

Medication Use in Pregnancy

Recommendation
  • In pregnancy medications must only be taken or stopped after consulting a physician.

Basis of the recommendations

Medications, whether prescription-only or over-the-counter, may affect the child. The overwhelming majority of medications have been insufficiently studied in terms of risks in pregnancy. In the consumption and prescription of medications, the individual risk to the mother from not receiving treatment must be weighed against the risks to the unborn child.


#

Background information

Substance-specific recommendations can be given in the course of a medical consultation. Where necessary, a dose adjustment or a switch of medication may be necessary even before conception. Necessary treatment must not be stopped because of wrong assumptions about harm to the unborn child.

Within the Pharmacovigilance Network of the Federal Institute for Drugs and Medical Devices (BfArM), the course of pregnancies for which the network has provided advice on medication use is documented and these data are evaluated jointly with similar centres in other European countries (ENTIS European Network of Territorial Information Services [https://www.entis-org.eu]). Information about the safety of medications in pregnancy and during breast-feeding is available via the website www.embryotox.de.

Women with chronic diseases who are planning a pregnancy require special medical counselling.


#
#

Preparation for Breast-Feeding

Recommendation
  • Expectant parents must be informed and given advice about breast-feeding because breast-feeding is best for mother and child.

Bases of the recommendation

A Cochrane review article comes to the conclusion that all forms of additional support have a positive effect on the increased duration of breast-feeding and the duration of exclusive breast-feeding [231]. The recommendation is consistent with recommendations on the promotion of breast-feeding in Germany [239] and in other countries [249].


#

Background information

Measures to support breast-feeding exert a positive effect on the initiation and duration of breast-feeding [231]. Since the motherʼs intention to breastfeed, an early latch and early initiation of breast-feeding are very important for successful breast-feeding and insecurities often lead to premature weaning [232], [233], [234], [235], [236], women and their partners should obtain breast-feeding counselling even during pregnancy. A positive attitude on the part of the partner also has a positive effect on the initiation and duration of breast-feeding [237], [238]. Professionals and trained lay people, personal (as opposed to telephone) support, four to eight contacts and settings with high initial breast-feeding rates can promote exclusive breast-feeding [241].

Although different forms of support in pregnancy and during the post partum period show positive effects on the attitude to breast-feeding, it is not possible to provide more specific details, e.g. in terms of measures or times [231], [240], [241], [242], [243], [244]. Counselling and support are more effective if they are offered not only for a short time, but where possible over the whole of the pregnancy until after the childʼs birth [245] and in an ambulatory as well as an inpatient setting [246].


#
#

Nutrition in Pregnancy for the Prevention of Allergies in the Child

Recommendations
  • Pregnant women must not exclude any foods from their diet to prevent allergies in the child. The avoidance of certain foods during pregnancy is not beneficial for the prevention of allergies in the child.

  • Pregnant women are recommended to consume oily fish regularly also with respect to allergy prevention.

Basis of the recommendations

The recommendations are based on current data and the German guidelines for allergy prevention of 2014 [247].


#

Background information

A low-allergen diet on the part of the mother during pregnancy does not lead to a reduced allergy risk in the child [248], [249]. Dietary restrictions are therefore not meaningful and can also be associated with the risk of insufficient nutrient intake. However, foods to which the woman herself exhibits an allergic reaction should also be avoided in pregnancy.

There is evidence that the consumption of sea fish and the long-chain omega-3 fatty acids that they contain during pregnancy and/or while breast-feeding has a protective effect against the development of atopic diseases in the child [250], [251]. Randomised controlled trials have shown that the risk of asthma is halved in children whose mothers had taken long-chain omega-3 fatty acids at doses greater than 2 g/day as a supplement during pregnancy [252], [253].

The consumption of prebiotics and probiotics during pregnancy does not offer any sufficiently proven benefits for allergy prevention in the child.

From the point of view of allergy prevention in the child as well, pregnant women should avoid smoking and areas where there is or has been smoking. In families with a medical history of allergies, the acquisition of cats should be avoided. Furthermore, pregnant women should avoid high exposure to air pollutants and mould accumulation in order to protect their health.


#
#

Oral and Dental Health

Recommendation
  • Women who are planning a pregnancy should have a dental check-up and where necessary undergo specific treatment.

Bases of the recommendation

Untreated maternal periodontitis has been associated in studies with an increased risk of premature birth and low birth weight [255], [256], [257], [258]). Mothers with untreated caries pass on caries-associated bacteria to their child [259], thus increasing the risk of caries in the child [256], [260]. Appropriate oral hygiene and a healthy diet for teeth reduce the caries-associated microflora. Dentist-supported caries prevention of the mother in pregnancy has the potential to reduce the later degree of caries in the child [261], [262].


#

Background information

Regular appropriate oral hygiene is one of the general health care measures and is recommended for all adults [254]. Altered defence reactions in the gingiva and hormonal changes in pregnancy (increased oestrogen and progesterone levels) encourage the development of inflammation of the gums (gingivitis), characterised by increased sensitivity and a tendency to bleeding [263]. Existing periodontitis can be exacerbated [263]. Whether treatment of periodontitis reduces the risk of premature birth and low birth weight cannot be answered with certainty due to contradictory study results [257], [258], [264].

Recommended dental and oral hygiene includes brushing the teeth with fluorinated toothpaste at least twice a day, carefully cleaning the gaps between the teeth with dental floss or interdental brushes once a day [254], [265] and having the teeth cleaned professionally at the dentistʼs at individually defined intervals. The frequency depends among other factors on the individual risk for caries and periodontitis [266]. The German Society of Periodontology (DG PARO) recommends supporting oral hygiene by professional teeth cleaning with oral hygiene instruction at the beginning and end of pregnancy [263].

Where diseases of the teeth and gums are present, the dentist should be consulted where possible even before the pregnancy. As well as preventive and diagnostic measures, preservative treatments can usually also be performed during pregnancy (such as the placement of fillings, fitting of individual crowns or treatment of periodontitis [255], [267]. As a rule amalgam fillings should not be placed during pregnancy [268]. In specific indications, amalgam fillings can be removed and replaced by other filling material.


#
#

Vaccinations

Recommendation
  • The vaccination status should be checked and vaccination gaps should be plugged in women who are planning a pregnancy.

Basis of the recommendation

Vaccine-preventable diseases during pregnancy increase the risk to the womanʼs health, can result in severe birth defects in the child and may be life-threatening for newborns. The Standing Committee on Vaccination at the Robert Koch Institute (STIKO) gives recommendations for women of childbearing age wishing to have a child, for women in pregnancy and for further contacts in the infantʼs immediate environment [269].


#

Background information

Complete protection against measles, rubella, varicella (chickenpox) and pertussis (whooping cough) is of particular importance in the family planning phase. The STIKO recommends the appropriate vaccinations for women wishing to have children. While dead vaccines (inactivated vaccines: killed pathogens or their constituents) can in principle be administered even in pregnancy, live vaccines (such as those for measles, mumps, rubella and varicella) are contraindicated for pregnant women. After each vaccination with a live vaccine, reliable contraception must be recommended one month. However, even if this period is not observed and even in the event of inadvertent vaccination in early pregnancy, no fetal damage as a result of these vaccinations is known to date [270].

Vaccinations not only protect the pregnant woman, who is more susceptible to infection due to hormonal changes than outside of pregnancy, but also the unborn or newborn child. Practically all viral infections in pregnancy are associated with an increased risk of abortions, birth defects, premature births and complications of pregnancy. In addition, pregnant women are themselves at increased risk, e.g. in the case of measles, of developing severe pneumonia.

There is a particularly high risk of severe disease courses in influenza infections in pregnancy. The STIKO has recommended vaccination against seasonal influenza for all pregnant women since 2010 [271], which also protects the neonate in the first few weeks of life against serious courses of diseases as a result of the maternal vaccine-induced antibodies, also known as “nest protection” [272].


#
#

Conclusion

A balanced diet, regular exercise and a healthy lifestyle are particularly important before and during pregnancy. The time before conception and the first 1000 days of the childʼs life provide an opportunity to lay the foundations for the health of the child, the expectant mother and the family. This potential for prevention should be recognised and utilised on a broad basis. The revised recommendations presented here provide uniform, practical and up-to-date knowledge-based recommendations for pregnancy and also for women/couples wishing to have a child.


#
#

Conflict of Interest/Interessenkonflikt

B. Koletzko, M. Cremer, M. Flothkötter, C. Graf, H. Hauner, C. Hellmers, M. Kersting, M. Krawinkel, M. Röbl-Mathieu, H. Przyrembel, U. Schiffner, K. Vetter, A. Weißenborn and A. Wöckel declare that there are no conflicts of interest under the terms of the guidelines of the Institute of Medicine. The work of BK was supported by grants from the Commission of the European Communities (FP5-QLRT-2001-00389 CHOPIN, FP5-QLAM-2001-00582 PIANO, FP6-007036QLRT-2001-00389 EARNEST, FP7-289346- EarlyNutrition), the European Research Council (Advanced Grant ERC-2012-AdG – no. 322605 META-GROWTH), the European Erasmus+ programme (Early Nutrition eAcademy Southeast Asia – 573651-EPP-1-2016-1-DE-EPPKA2-CBHE-JP and Capacity Building to Improve Early Nutrition and Health in South Africa – 598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP) and the European Interreg programme (Focus in CD – CE111). Additional funding came from the German Federal Ministry of Education and Research (No. 01 GI 0825), the German Research Foundation (KO912/10-1), the McHealth innovation initiative of the Ludwig Maximilian University of Munich (LMU) and the Centre for Advanced Studies of the LMU. The LMU and its employee BK have worked with pharmaceutical food companies on scientific and educational projects, the majority of which were state-supported research projects. None of these interactions had any influence on the contents of this manuscript./
B. Koletzko, M. Cremer, M. Flothkötter, C. Graf, H. Hauner, C. Hellmers, M. Kersting, M. Krawinkel, M. Röbl-Mathieu, H. Przyrembel, U. Schiffner, K. Vetter, A. Weißenborn und A. Wöckel erklären, dass kein Interessenkonflikt im Sinne der Richtlinien des Institute of Medicine besteht. Die Arbeit von BK wird durch finanzielle Förderung der Kommission der Europäischen Gemeinschaften (FP5-QLRT-2001-00389 CHOPIN, FP5-QLAM-2001-00582 PIANO, FP6-007036QLRT-2001-00389 EARNEST, FP7-289346- EarlyNutrition), das European Research Council (Advanced Grant ERC-2012-AdG – no. 322605 META-GROWTH), das europäische Erasmus+ Programm (Early Nutrition eAcademy Southeast Asia – 573651-EPP-1-2016-1-DE-EPPKA2-CBHE-JP und Capacity Building to Improve Early Nutrition and Health in South Africa – 598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP) und das europäische Interreg-Programm (Focus in CD – CE111) unterstützt. Zusätzliche Förderung erfolgte durch das Bundesministerium für Bildung und Forschung (Nr. 01 GI 0825), die Deutsche Forschungsgemeinschaft (KO912/10-1), die Innovationsinitiative McHealth der Ludwig-Maximilians-Universität München (LMU) und das Center for Advanced Studies der LMU. Die LMU und ihr Mitarbeiter BK haben bei wissenschaftlichen und edukativen Projekten mit pharmazeutischen Nahrungsmittel-Unternehmen zusammengearbeitet, überwiegend als Teil öffentlich geförderter Forschungsprojekte. Keine dieser Interaktionen hat Einfluss auf den Inhalt dieses Manuskriptes genommen.

Acknowledgements

The Healthy Start – Young Family Network and the authors thank Uta Engels (University of Regensburg), Nina Ferrari (University Hospital Cologne), Thomas Kauth (Ludwigsburg), Lucilla Poston (Kings College London), Marion Sulprizio (German Sport University Cologne) and Janina Goletzke (Hamburg-Eppendorf University Hospital) for their technical support and their valuable contributions to the discussion.

1 The term “parents” encompasses all forms of relationships in which there is a wish to have children or in which a woman is pregnant.


2 The following key words (Mesh terms and title/abstract) in various spellings and truncations were searched for in the databases: diet/nutrition, energy/nutrient requirement, reference value, exercise/physical activity/sports, body weight/gestational weight gain/body weight changes, alcohol/alcohol consumption AND childbearing/gestation/gravidity/pregnancy, reproductive planning/pregnancy planning/pre gestation. The search was confined to meta-analyses, systematic reviews and guidelines/consensus development conferences since 2012.


Supporting Information

Ergänzendes Material

  • References/Literatur

  • 1 Koletzko B, Schiess S, Brands B. et al. [Infant feeding practice and later obesity risk. Indications for early metabolic programming]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2010; 53: 666-673
  • 2 Bundesministerium für Gesundheit. Nationales Gesundheitsziel – Gesundheit rund um die Geburt. Online: https://www.bundesregierung.de/Content/Infomaterial/BMG/_3005.html?view=trackDownload last access: 31.07.2018
  • 3 Röbl-Mathieu M. Preconception Counselling. Frauenarzt 2013; 54: 966-972
  • 4 Hanson MA, Bardsley A, De-Regil LM. et al. The International Federation of Gynecology and Obstetrics (FIGO) recommendations on adolescent, preconception, and maternal nutrition: “Think Nutrition First”. Int J Gynaecol Obstet 2015; 131 (Suppl. 04) S213-S253
  • 5 Mensink GBM, Schienkiewitz A, Haftenberger M. et al. Übergewicht und Adipositas in Deutschland. Ergebnisse der Studie zur Gesundheit Erwachsener in Deutschland (DEGS1). Bundesgesundheitsbl 2013; 56: 786-794
  • 6 Stubert J, Reister F, Hartmann S. et al. Risiken bei Adipositas in der Schwangerschaft. Dtsch Arztebl Int 2018; 115: 276-282
  • 7 Davies SC. Annual Report of the Chief Medical Officer, 2014, The Health of the 51 %: Women. London: Department of Health; 2015
  • 8 Melchior H, Kurch-Bek D, Mund J. The prevalence of gestational diabetes. Dtsch Arztebl Int 2017; 114: 412-418
  • 9 Schoenaker DA, Mishra GD, Callaway LK. et al. The Role of Energy, Nutrients, Foods, and Dietary Patterns in the Development of Gestational Diabetes Mellitus: A Systematic Review of Observational Studies. Diabetes Care 2016; 39: 16-23
  • 10 Bennett CJ, Walker RE, Blumfield ML. et al. Interventions designed to reduce excessive gestational weight gain can reduce the incidence of gestational diabetes mellitus: A systematic review and meta-analysis of randomised controlled trials. Diabetes Res Clin Pract 2018; 141: 69-79
  • 11 Orth B, Töppich J. Rauchen bei Jugendlichen und jungen Erwachsenen in Deutschland 2014. Ergebnisse einer aktuellen Repräsentativbefragung und Trends. Online: https://www.bzga.de/forschung/studien-untersuchungen/studien/suchtpraevention/?sub=90 last access: 29.12.2017
  • 12 Die Drogenbeauftragte der Bundesregierung Bundesministerium für Gesundheit. Hrsg. Drogen- und Suchtbericht Juni 2016. Online: https://www.drogenbeauftragte.de/fileadmin/dateien-dba/Drogenbeauftragte/4_Presse/1_Pressemitteilungen/2016/2016_2/160928_Drogenbericht-2016_NEU_Sept.2016.pdf last access: 31.07.2018
  • 13 Koletzko B, Bauer CP, Bung P. et al. [Nutrition in pregnancy – Practice recommendations of the Network „Healthy Start – Young Family Network“]. Dtsch Med Wochenschr 2012; 137: 1366-1372
  • 14 Stephenson J, Heslehurst N, Hall J. et al. Before the beginning: nutrition and lifestyle in the preconception period and its importance for future health. Lancet 2018; 391: 1830-1841
  • 15 Bundeszentrale für gesundheitliche Aufklärung. frauen leben 3. Familienplanung im Leben von Frauen. Schwerpunkt: Ungewollte Schwangerschaften. Köln: Bundeszentrale für gesundheitliche Aufklärung; 2016
  • 16 Zhang C, Wu Y, Li S. et al. Maternal prepregnancy obesity and the risk of shoulder dystocia: a meta-analysis. BJOG 2017; DOI: 10.1111/1471-0528.14841.
  • 17 Balsells M, Garcia-Patterson A, Corcoy R. Systematic review and meta-analysis on the association of prepregnancy underweight and miscarriage. Eur J Obstet Gynecol Reprod Biol 2016; 207: 73-79
  • 18 Meehan S, Beck CR, Mair-Jenkins J. et al. Maternal obesity and infant mortality: a meta-analysis. Pediatrics 2014; 133: 863-871
  • 19 World Health Organization Regional Office for Europe. Good maternal Nutrition. The best Start in Life. Copenhagen, Denmark: WHO Regional Office for Europe; 2016
  • 20 Gaudet L, Ferraro ZM, Wen SW. et al. Maternal obesity and occurrence of fetal macrosomia: a systematic review and meta-analysis. Biomed Res Int 2014; 2014: 640291
  • 21 OʼConnor DL, Blake J, Bell R. et al. Nutrition Working Group. Canadian Consensus on Female Nutrition: Adolescence, Reproduction, Menopause, and Beyond. J Obstet Gynaecol Can 2016; 38: 508-554.e18
  • 22 National Institute for Health and Clinical Excellence. Weight management before, during and after pregnancy. Online: https://www.nice.org.uk/guidance/ph27/resources/weight-management-before-during-and-after-pregnancy-pdf-1996242046405 last access: 16.11.2017
  • 23 Dudenhausen JW, Grunebaum A, Kirschner W. Prepregnancy body weight and gestational weight gain-recommendations and reality in the USA and in Germany. Am J Obstet Gynecol 2015; 213: 591-592
  • 24 Beyerlein A, Lack N, von Kries R. Within-population average ranges compared with Institute of Medicine recommendations for gestational weight gain. Obstet Gynecol 2010; 116: 1111-1118
  • 25 World Health Organization, Food and Agriculture Organization of the United Nations, University UN. Human energy requirements. Report of a Joint FAO/WHO/UNU Expert Consultation, Rome, Italy, 17 – 24 October 2001. Rome: WHO; 2004
  • 26 Goldberg GR. Nutrition in pregnancy: the facts and fallacies. Nurs Stand 2003; 17: 39-42
  • 27 Rasmussen KM, Yaktin AL. Committee to reexamine IOM Pregnancy Weight Guidelines. Weight Gain during Pregnancy: reexamining the Guidelines. Washington (DC): Institute of Medicine (US) and National Research Council (US); 2009
  • 28 Goldstein RF, Abell SK, Ranasinha S. et al. Association of Gestational Weight Gain With Maternal and Infant Outcomes: A Systematic Review and Meta-analysis. JAMA 2017; 317: 2207-2225
  • 29 Margerison Zilko CE, Rehkopf D, Abrams B. Association of maternal gestational weight gain with short- and long-term maternal and child health outcomes. Am J Obstet Gynecol 2010; 202: 574.e1-574.e8
  • 30 Scott C, Andersen CT, Valdez N. et al. No global consensus: a cross-sectional survey of maternal weight policies. BMC Pregnancy Childbirth 2014; 14: 167
  • 31 Alavi N, Haley S, Chow K. et al. Comparison of national gestational weight gain guidelines and energy intake recommendations. Obes Rev 2013; 14: 68-85
  • 32 Blake-Lamb TL, Locks LM, Perkins ME. et al. Interventions for Childhood Obesity in the First 1,000 Days A Systematic Review. Am J Prev Med 2016; 50: 780-789
  • 33 Nicklas JM, Barbour LA. Optimizing Weight for Maternal and Infant Health – Tenable, or Too Late?. Expert Rev Endocrinol Metab 2015; 10: 227-242
  • 34 Boney CM, Verma A, Tucker R. et al. Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics 2005; 115: e290-e296
  • 35 Reynolds RM, Allan KM, Raja EA. et al. Maternal obesity during pregnancy and premature mortality from cardiovascular event in adult offspring: follow-up of 1 323 275 person years. BMJ 2013; 347: f4539
  • 36 Vinturache A, McKeating A, Daly N. et al. Maternal body mass index and the prevalence of spontaneous and elective preterm deliveries in an Irish obstetric population: a retrospective cohort study. BMJ Open 2017; 7: e015258
  • 37 Hoellen F, Hornemann A, Haertel C. et al. Does maternal underweight prior to conception influence pregnancy risks and outcome?. In Vivo 2014; 28: 1165-1170
  • 38 Shin D, Song WO. Prepregnancy body mass index is an independent risk factor for gestational hypertension, gestational diabetes, preterm labor, and small- and large-for-gestational-age infants. Matern Fetal Neonatal Med 2015; 28: 1679-1686
  • 39 Busetto L, Dicker D, Azran C. et al. Practical Recommendations of the Obesity Management Task Force of the European Association for the Study of Obesity for the Post-Bariatric Surgery Medical Management. Obes Facts 2017; 10: 597-632
  • 40 Deutsche Adipositas-Gesellschaft (DAG) e.V., Deutsche Diabetes Gesellschaft (DDG), Deutsche Gesellschaft für Ernährung (DGE) e.V.. et al Interdisziplinäre Leitlinie der Qualität S3 zur „Prävention und Therapie der Adipositas“. Online: http://www.adipositas-gesellschaft.de/fileadmin/PDF/Leitlinien/S3_Adipositas_Praevention_Therapie_2014.pdf last access: 28.05.2018
  • 41 Kwong W, Tomlinson G, Feig DS. Maternal and neonatal outcomes after bariatric surgery; a systematic review and meta-analysis: do the benefits outweigh the risks?. Am J Obstet Gynecol 2018; 218: 573-580
  • 42 Jaddoe VWV. Persönliche Mitteilung. 2018
  • 43 Beyerlein A, Schiessl B, Lack N. et al. Optimal gestational weight gain ranges for the avoidance of adverse birth weight outcomes: a novel approach. Am J Clin Nutr 2009; 90: 1552-1558
  • 44 Rogozinska E, Marlin N, Jackson L. et al. Effects of antenatal diet and physical activity on maternal and fetal outcomes: individual patient data meta-analysis and health economic evaluation. Health Technol Assess 2017; 21: 1-158
  • 45 Dodd JM, Turnbull D, McPhee AJ. et al. Antenatal lifestyle advice for women who are overweight or obese: LIMIT randomised trial. BMJ 2014; 348: g1285
  • 46 Poston L, Bell R, Croker H. et al. Effect of a behavioural intervention in obese pregnant women (the UPBEAT study): a multicentre, randomised controlled trial. Lancet Diabetes Endocrinol 2015; 3: 767-777
  • 47 International Weight Management in Pregnancy Collaborative Group. Effect of diet and physical activity based interventions in pregnancy on gestational weight gain and pregnancy outcomes: meta-analysis of individual participant data from randomised trials. BMJ 2017; 358: j3119
  • 48 Starling AP, Brinton JT, Glueck DH. et al. Associations of maternal BMI and gestational weight gain with neonatal adiposity in the Healthy Start study. Am J Clin Nutr 2015; 101: 302-309
  • 49 Tan HC, Roberts J, Catov J. et al. Motherʼs pre-pregnancy BMI is an important determinant of adverse cardiometabolic risk in childhood. Pediatr Diabetes 2015; 16: 419-426
  • 50 Plachta-Danielzik S, Kehden B, Landsberg B. et al. Attributable risks for childhood overweight: evidence for limited effectiveness of prevention. Pediatrics 2012; 130: e865-e871
  • 51 EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA). Scientific Opinion on Dietary Reference Values for energy. EFSA Journal 2013; 11: 3005
  • 52 Deutsche Gesellschaft für Ernährung (DGE); Österreichische Gesellschaft für Ernährung (ÖGE), Schweizerische Gesellschaft für Ernährung (SGE). Referenzwerte für die Nährstoffzufuhr. Bonn: 2017
  • 53 Ferrari N, Graf C. Bewegungsempfehlungen für Frauen während und nach der Schwangerschaft. Gesundheitswesen 2017; 79: S36-S39
  • 54 Cantwell R, Clutton-Brock T, Cooper G. et al. Saving Mothersʼ Lives: Reviewing maternal deaths to make motherhood safer: 2006–2008. The Eighth Report of the Confidential Enquiries into Maternal Deaths in the United Kingdom. BJOG 2011; 118 (Suppl. 01) 1-203
  • 55 Catalano PM. Obesity, insulin resistance, and pregnancy outcome. Reproduction 2010; 140: 365-371
  • 56 Rasmussen KM, Abrams B, Bodnar LM. et al. Recommendations for weight gain during pregnancy in the context of the obesity epidemic. Obstet Gynecol 2010; 116: 1191-1195
  • 57 Tielemans MJ, Garcia AH, Peralta Santos A. et al. Macronutrient composition and gestational weight gain: a systematic review. Am J Clin Nutr 2016; 103: 83-99
  • 58 FAO/WHO/UNU Expert Consultation. Human energy requirements: report of a joint FAO/WHO/UNU Expert Consultation. Food Nutr Bull 2005; 26: 166
  • 59 Lof M. Physical activity pattern and activity energy expenditure in healthy pregnant and non-pregnant Swedish women. Eur J Clin Nutr 2011; 65: 1295-1301
  • 60 Rauh K, Gabriel E, Kerschbaum E. et al. Safety and efficacy of a lifestyle intervention for pregnant women to prevent excessive maternal weight gain: a cluster-randomized controlled trial. BMC Pregnancy Childbirth 2013; 13: 151
  • 61 Berti C, Biesalski HK, Gartner R. et al. Micronutrients in pregnancy: current knowledge and unresolved questions. Clini Nutr 2011; 30: 689-701
  • 62 Forschungsinstitut für Kinderernährung. Hrsg. Empfehlungen für die Ernährung von Mutter und Kind. Dortmund: Forschungsinstitut für Kinderernährung; 2016
  • 63 Deutsche Gesellschaft für Ernährung. Vollwertig essen und trinken nach den 10 Regeln der DGE. Online: http://www.dge.de/ernaehrungspraxis/vollwertige-ernaehrung/10-regeln-der-dge/ last access: 20.11.2017
  • 64 The American Society for Reproductive Medicine. Optimizing natural fertility: a committee opinion. Practice Committee of the American Society for Reproductive Medicine in collaboration with the Society for Reproductive Endocrinology and Infertility. Fertil Steril 2013; 100: 631-637
  • 65 Poston L, Bell R, Briley AL. et al. Improving Pregnancy Outcome in obese Women: the UK Pregnancies Better Eating and Activity randomised controlled Trial. Southampton (UK): NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House; 2017
  • 66 Koletzko B, Brands B, Grote V. et al. Long-Term Health Impact of Early Nutrition: The Power of Programming. Ann Nutr Metab 2017; 70: 161-169
  • 67 Thangaratinam S, Rogozinska E, Jolly K. et al. Effects of interventions in pregnancy on maternal weight and obstetric outcomes: meta-analysis of randomised evidence. BMJ 2012; 344: e2088
  • 68 Harrison CL, Lombard CB, Strauss BJ. et al. Optimizing healthy gestational weight gain in women at high risk of gestational diabetes: a randomized controlled trial. Obesity 2013; 21: 904-909
  • 69 Zhang R, Han S, Chen GC. et al. Effects of low-glycemic-index diets in pregnancy on maternal and newborn outcomes in pregnant women: a meta-analysis of randomized controlled trials. Eur J Nutr 2018; 57: 167-177
  • 70 Deutsche Gesellschaft für Ernährung. Ausgewählte Fragen und Antworten zu Folat. Online: https://www.dge.de/wissenschaft/weitere-publikationen/faqs/folat/ last access: 24.07.2018
  • 71 EFSA Panel on Contaminants in the Food Chain. Opinion of the Scientific Panel on Contaminants in the Food Chain on a request from the Commission related to mercury and methylmercury in food. EFSA Journal 2004; 34: 1-14
  • 72 Piccoli GB, Clari R, Vigotti FN. et al. Vegan-vegetarian diets in pregnancy: danger or panacea? A systematic narrative review. BJOG 2015; 122: 623-633
  • 73 Richter M, Boeing H, Grünewald-Funk D. et al. Vegane Ernährung. Position der Deutschen Gesellschaft für Ernährung e. V. (DGE). Ernährungs Umschau 2016; 63: 92-102
  • 74 Dror DK, Allen LH. Effect of vitamin B12 deficiency on neurodevelopment in infants: current knowledge and possible mechanisms. Nutr Rev 2008; 66: 250-255
  • 75 Honzik T, Adamovicova M, Smolka V. et al. Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B12 deficiency–what have we learned?. Eur J Paediatr Neurol 2010; 14: 488-495
  • 76 von Schenck U, Bender-Gotze C, Koletzko B. Persistence of neurological damage induced by dietary vitamin B-12 deficiency in infancy. Arch Dis Child 1997; 77: 137-139
  • 77 Wada L, King JC. Trace element nutrition during pregnancy. Clin Obstet Gynecol 1994; 37: 574-586
  • 78 Wagener IE, Bergmann RL, Kamtsiuris P. et al. Prävalenz und Risikofaktoren für Eisenmangel bei jungen Müttern. Gesundheitswesen 2000; 62: 176-178
  • 79 King JC, Stein T, Doyle M. Effect of vegetarianism on the zinc status of pregnant women. Am J Clin Nutr 1981; 34: 1049-1055
  • 80 Koebnick C, Hoffmann I, Dagnelie PC. et al. Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women. J Nutr 2004; 134: 3319-3326
  • 81 Czeizel AE, Dudas I, Paput L. et al. Prevention of neural-tube defects with periconceptional folic acid, methylfolate, or multivitamins?. Ann Nutr Metab 2011; 58: 263-271
  • 82 De-Regil LM, Pena-Rosas JP, Fernandez-Gaxiola AC. et al. Effects and safety of periconceptional oral folate supplementation for preventing birth defects. Cochrane Database Syst Rev 2015; (12) CD007950 DOI: 10.1002/14651858.CD007950.pub3.
  • 83 Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 1992; 327: 1832-1835
  • 84 Viswanathan M, Treiman KA, Doto JK. et al. Folic Acid Supplementation: An Evidence Review for the U.S. Preventive Services Task Force. Rockville (MD): Agency for Healthcare Research and Quality (US); 2017
  • 85 [Anonym] Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet 1991; 338: 131-137
  • 86 Obeid R, Pietrzik K. Neuralrohrdefekte: Das Veto gegen Folsäure im Mehl sollte überdacht werden. Dtsch Arztebl 2018; 115 (27-28): A-1329/B-1123/C-1115
  • 87 Koletzko B, Pietrzik K. Gesundheitliche Bedeutung der Folsäurezufuhr. Dtsch Arztebl 2004; 101: A-1670/B-1388/C-1338
  • 88 Deutsche Gesellschaft für Ernährung, Deutsche Gesellschaft für Humangenetik, Deutsche Gesellschaft für Kinderheilkunde. et al. Prävention von Neuralrohrdefekten durch Folsäurezufuhr in der Frühschwangerschaft. Der Frauenarzt 1994; 35: 1007–1010. Nachdruck in: Der Kinderarzt 1995; 26: 187–190; .2: ASbH-Brief – Zeitschrift der Arbeitsgemeinschaft Spina bifida und Hydrocephalus e. V.; .3: 1995; 1995;. Monatsschr Kinderheilkd 1995; 143: 1003-1005
  • 89 Krawinkel MB, Strohm D, Weissenborn A. et al. Revised D-A-CH intake recommendations for folate: how much is needed?. Eur J Clin Nutr 2014; 68: 719-723
  • 90 Gomes S, Lopes C, Pinto E. Folate and folic acid in the periconceptional period: recommendations from official health organizations in thirty-six countries worldwide and WHO. Public Health Nutr 2016; 19: 176-189
  • 91 Australian Government Department of Health. Clinical Practice Guidelines: Pregnancy Care. Online: http://www.health.gov.au/internet/main/publishing.nsf/Content/pregnancycareguidelines last access: 26.07.2018
  • 92 Bramswig S, Prinz-Langenohl R, Lamers Y. et al. Supplementation with a multivitamin containing 800 microg of folic acid shortens the time to reach the preventive red blood cell folate concentration in healthy women. Int J Vitam Nutr Res 2009; 79: 61-70
  • 93 Obeid R, Schon C, Wilhelm M. et al. The effectiveness of daily supplementation with 400 or 800 microg/day folate in reaching protective red blood folate concentrations in non-pregnant women: a randomized trial. Eur J Nutr 2017; DOI: 10.1007/s00394-017-1461-8.
  • 94 World Health Organization. Guideline: Optimal Serum and Red Blood Cell Folate Concentrations in Women of reproductive Age for Prevention of neural Tube Defects. Geneva: WHO; 2015
  • 95 Max Rubner Institut. Nationale Verzehrsstudie II, Ergebnisbericht. Karlsruhe: Bundesforschungsinstitut für Ernährung und Lebensmittel; 2008
  • 96 Mensink G, Weißenborn A, Richter A. Ernährungssituation in Deutschland. Folat. In: Deutsche Gesellschaft für Ernährung. Hrsg. 13 DGE-Ernährungsbericht. Bonn: Deutsche Gesellschaft für Ernährung; 2016
  • 97 Pietrzik K, Lamers Y, Bramswig S. et al. Calculation of red blood cell folate steady state conditions and elimination kinetics after daily supplementation with various folate forms and doses in women of childbearing age. Am J Clin Nutr 2007; 86: 1414-1419
  • 98 Scientific Committee on Food, European Commission. Opinion of the Scientific Committee on Food on the tolerable upper intake level of folate. Brüssel: Europäische Kommission; 2000
  • 99 Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes and its Panel on Folate OBV, and Choline. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington (DC): National Academies Press (US) National Academy of Sciences; 1998
  • 100 Oliver EM, Grimshaw KE, Schoemaker AA. et al. Dietary habits and supplement use in relation to national pregnancy recommendations: data from the EuroPrevall birth cohort. Matern Child Health J 2014; 18: 2408-2425
  • 101 Egen V, Hasford J. Prevention of neural tube defects: effect of an intervention aimed at implementing the official recommendations. Sozial- und Praventivmedizin 2003; 48: 24-32
  • 102 Kowoll S, Kurzenhäuser-Carstens S, Martin A. et al. Folsäure zur Prävention von Neuralrohrdefekten – Wissen und Einstellungen sowie Beratungs- und Einnahmepraxis in Berlin. Z Geburtshilfe Neonatol 2015; DOI: 10.1055/s-005-30402.
  • 103 Becker S, Schmid D, Amann-Gassner U. et al. Verwendung von Nährstoffsupplementen vor und während der Schwangerschaft. Ernährungs Umschau 2011; 58: 36-41
  • 104 World Health Organization. Urinary iodine concentrations for determing iodine status in population. Online: http://apps.who.int/iris/bitstream/10665/85972/1/WHO_NMH_NHD_EPG_13.1_eng.pdf last access: 24.11.2017
  • 105 Deutsche Gesellschaft für Ernährung. Hrsg. 13. Ernährungsbericht. Bonn: Deutsche Gesellschaft für Ernährung; 2016
  • 106 Gemeinsamer Bundesausschuss. Richtlinien des Gemeinsamen Bundesausschusses über die ärztliche Betreuung während der Schwangerschaft und nach der Entbindung („Mutterschafts-Richtlinien“) in der Fassung vom 10. Dezember 1985 (veröffentlicht im Bundesanzeiger Nr. 60 a vom 27. März 1986), zuletzt geändert am 21. April 2016, veröffentlicht im Bundesanzeiger AT 19.07.2016 B5, in Kraft getreten am 20. Juli 2016. Bundesanzeiger 2016; AT 19.07.2016.
  • 107 Alexander EK, Pearce EN, Brent GA. et al. 2017 Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and the Postpartum. Thyroid 2017; 27: 315-389
  • 108 Australian Government National Health and Medical Research Council (NHMRC). NHMRC Public Statement: Iodine Supplementation for Pregnant and Breastfeeding Women. 2010. Online: https://www.nhmrc.gov.au/guidelines-publications/new45 last access: 24.11.2017
  • 109 Taylor PN, Vaidya B. Iodine supplementation in pregnancy – is it time?. Clin Endocrinol (Oxf) 2016; 85: 10-14
  • 110 EFSA NDA Panel (EFSA Panel on Panel on Dietetic Products Nutrition and Allergies). Scientific Opinion on Dietary Reference Values for iodine. EFSA Journal 2014; 12: 3660
  • 111 Bath SC, Steer CD, Golding J. et al. Effect of inadequate iodine status in UK pregnant women on cognitive outcomes in their children: results from the Avon Longitudinal Study of Parents and Children (ALSPAC). Lancet 2013; 382: 331-337
  • 112 Bougma K, Aboud FE, Harding KB. et al. Iodine and mental development of children 5 years old and under: a systematic review and meta-analysis. Nutrients 2013; 5: 1384-1416
  • 113 Rayman MP, Bath SC. The new emergence of iodine deficiency in the UK: consequences for child neurodevelopment. Ann Clin Biochem 2015; 52: 705-708
  • 114 Trumpff C, De Schepper J, Tafforeau J. et al. Mild iodine deficiency in pregnancy in Europe and its consequences for cognitive and psychomotor development of children: a review. J Trace Elem Med Biol 2013; 27: 174-183
  • 115 Ghassabian A, Henrichs J, Tiemeier H. Impact of mild thyroid hormone deficiency in pregnancy on cognitive function in children: lessons from the Generation R Study. Best Pract Res Clin Endocrinol Metab 2014; 28: 221-232
  • 116 Abel MH, Caspersen IH, Meltzer HM. et al. Suboptimal Maternal Iodine Intake Is Associated with Impaired Child Neurodevelopment at 3 Years of Age in the Norwegian Mother and Child Cohort Study. J Nutr 2017; 147: 1314-1324
  • 117 Redman K, Ruffman T, Fitzgerald P. et al. Iodine Deficiency and the Brain: Effects and Mechanisms. Crit Rev Food Sci Nutr 2016; 56: 2695-2713
  • 118 Taylor PN, Okosieme OE, Dayan CM. et al. Therapy of endocrine disease: Impact of iodine supplementation in mild-to-moderate iodine deficiency: systematic review and meta-analysis. Eur J Endocrinol 2014; 170: R1-R15
  • 119 Harding KB, Pena-Rosas JP, Webster AC. et al. Iodine supplementation for women during the preconception, pregnancy and postpartum period. Cochrane Database Syst Rev 2017; (03) CD011761
  • 120 Zhou SJ, Anderson AJ, Gibson RA. et al. Effect of iodine supplementation in pregnancy on child development and other clinical outcomes: a systematic review of randomized controlled trials. Am J Clin Nutr 2013; 98: 1241-1254
  • 121 Bundesinstitut für Risikobewertung. Gesundheitliche Risiken durch zu hohen Jodgehalt in getrockneten Algen. Aktualisierte Stellungnahme Nr. 026/2007 des BfR vom 22. Juni 2004, aktualisiert am 12. Juni 2007. 2007. Online: https://www.bfr.bund.de/cm/343/gesundheitliche_risiken_durch_zu_hohen_jodgehalt_in_getrockneten_algen.pdf last access: 24.11.2017
  • 122 Bouga M, Combet E. Emergence of Seaweed and Seaweed-Containing Foods in the UK: Focus on Labeling, Iodine Content, Toxicity and Nutrition. Foods (Basel, Switzerland) 2015; 4: 240-253
  • 123 Pena-Rosas JP, De-Regil LM, Garcia-Casal MN. et al. Daily oral iron supplementation during pregnancy. Cochrane Database Syst Rev 2015; (07) CD004736 DOI: 10.1002/14651858.CD004736.pub5.
  • 124 Vucic V, Berti C, Vollhardt C. et al. Effect of iron intervention on growth during gestation, infancy, childhood, and adolescence: a systematic review with meta-analysis. Nutr Rev 2013; 71: 386-401
  • 125 McDonagh M, Cantor A, Bougatsos C. et al. In: Routine Iron Supplementation and Screening for Iron Deficiency Anemia in Pregnant Women: A Systematic Review to Update the US Preventive Services Task Force Recommendation. Rockville (MD): Agency for Healthcare Research and Quality (US); 2015
  • 126 Milman N. Oral iron prophylaxis in pregnancy: not too little and not too much!. J Pregnancy 2012; 2012: 514345
  • 127 Hwang JY, Lee JY, Kim KN. et al. Maternal iron intake at mid-pregnancy is associated with reduced fetal growth: results from Mothers and Childrenʼs Environmental Health (MOCEH) study. Nutr J 2013; 12: 38
  • 128 NIHR Dissemination Centre. Better Beginnings. Improving Health for Pregnancy. Themed Review. Online: http://www.dc.nihr.ac.uk/themed-reviews/Better-beginnings-web-interactive.pdf last access: 23.01.2018
  • 129 Haute Autorité de Santé. Comment mieux informer les femmes enceintes?. Online: https://www.has-sante.fr/portail/jcms/c_268522/fr/information-femmes-enceintes-recommandations-pdf last access: 31.07.2018
  • 130 Institute of Obstetricians & Gynaecologists RCoPoI, Directorate of Clinical Strategy and Programmes, Health Service Executiv. Clinical Practice Guideline: Nutrition for Pregnancy. Online: https://rcpi-live-cdn.s3.amazonaws.com/wp-content/uploads/2016/05/22.-Nutrition-during-Pregnancy.pdf last access: 31.07.2018
  • 131 World Health Organization. Guideline: Intermittent Iron and Folic Acid Supplementation in Non-Anaemic Pregnant Women. Geneva: WHO; 2012
  • 132 EFSA Panel on Dietetic Products, Nutrition and Allergies. Scientific Opinion on Dietary Reference Values for fats, including saturated fatty acids, polyunsaturated fatty acids, monounsaturated fatty acids, trans fatty acids, and cholesterol. EFSA Journal 2010; DOI: 10.2903/j.efsa.2010.1461.
  • 133 Koletzko B, Lien E, Agostoni C. et al. The roles of long-chain polyunsaturated fatty acids in pregnancy, lactation and infancy: review of current knowledge and consensus recommendations. J Perinat Med 2008; 36: 5-14
  • 134 Menon KC, Ferguson EL, Thomson CD. et al. Effects of anemia at different stages of gestation on infant outcomes. Nutrition 2016; 32: 61-65
  • 135 Scholl TO, Hediger ML, Fischer RL. et al. Anemia vs. iron deficiency: increased risk of preterm delivery in a prospective study. Am J Clin Nutr 1992; 55: 985-988
  • 136 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA)). Scientific Opinion on Dietary Reference Values for iron. EFSA Journal 2015; 13: 4254
  • 137 Bergmann RL, Dudenhausen JW, Ennen JC. et al. Diagnostik und Behandlung der Anämie und des Eisenmangels in der Schwangerschaft und im Wochenbett. Geburtshilfe Frauenheilkd 2009; 69: 682-686
  • 138 Burdge GC, Tan SY, Henry CJ. Long-chain n-3 PUFA in vegetarian women: a metabolic perspective. J Nutr Sci 2017; 6: e58
  • 139 Glaser C, Lattka E, Rzehak P. et al. Genetic variation in polyunsaturated fatty acid metabolism and its potential relevance for human development and health. Matern Child Nutr 2011; 7 (Suppl. 02) 27-40
  • 140 Lattka E, Klopp N, Demmelmair H. et al. Genetic variations in polyunsaturated fatty acid meatbolism-implixations for child health?. Ann Nutr Metab 2012; 60: 8-17
  • 141 Koletzko B, Boey CC, Campoy C. et al. Current information and Asian perspectives on long-chain polyunsaturated fatty acids in pregnancy, lactation, and infancy: systematic review and practice recommendations from an early nutrition academy workshop. Ann Nutr Metab 2014; 65: 49-80
  • 142 Brenna JT. Efficiency of conversion of alpha-linolenic acid to long chain n-3 fatty acids in man. Curr Opin Clin Nutr Metab Care 2002; 5: 127-132
  • 143 Brenna JT, Salem jr. N, Sinclair AJ. et al. alpha-Linolenic acid supplementation and conversion to n-3 long-chain polyunsaturated fatty acids in humans. Prostaglandins Leukot Essent Fatty Acids 2009; 80: 85-91
  • 144 Barcelo-Coblijn G, Murphy EJ. Alpha-linolenic acid and its conversion to longer chain n-3 fatty acids: benefits for human health and a role in maintaining tissue n-3 fatty acid levels. Prog Lipid Res 2009; 48: 355-374
  • 145 Kar S, Wong M, Rogozinska E. et al. Effects of omega-3 fatty acids in prevention of early preterm delivery: a systematic review and meta-analysis of randomized studies. Eur J Obstet Gynecol Reprod Biol 2016; 198: 40-46
  • 146 Makrides M, Duley L, Olsen SF. Marine oil, and other prostaglandin precursor, supplementation for pregnancy uncomplicated by pre-eclampsia or intrauterine growth restriction. Cochrane Database Syst Rev 2006; (03) CD003402 DOI: 10.1002/14651858.CD003402.pub2.
  • 147 Yelland LN, Gajewski BJ, Colombo J. et al. Predicting the effect of maternal docosahexaenoic acid (DHA) supplementation to reduce early preterm birth in Australia and the United States using results of within country randomized controlled trials. Prostaglandins Leukot Essent Fatty Acids 2016; 112: 44-49
  • 148 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA)). Scientific Opinion on the substantiation of a health claim related to DHA and contribution to normal brain development pursuant to Article 14 of Regulation (EC) No 1924/2006. EFSA Journal 2014; 12: 3840
  • 149 Julvez J, Mendez M, Fernandez-Barres S. et al. Maternal Consumption of Seafood in Pregnancy and Child Neuropsychological Development: A Longitudinal Study Based on a Population With High Consumption Levels. Am J Epidemiol 2016; 183: 169-182
  • 150 Hibbeln JR, Davis JM, Steer C. et al. Maternal seafood consumption in pregnancy and neurodevelopmental outcomes in childhood (ALSPAC study): an observational cohort study. Lancet 2007; 369: 578-585
  • 151 Oken E, Radesky JS, Wright RO. et al. Maternal fish intake during pregnancy, blood mercury levels, and child cognition at age 3 years in a US cohort. Am J Epidemiol 2008; 167: 1171-1181
  • 152 Steer CD, Lattka E, Koletzko B. et al. Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age. Am J Clin Nutr 2013; 98: 1575-1582
  • 153 Braarud HC, Markhus MW, Skotheim S. et al. Maternal DHA Status during Pregnancy Has a Positive Impact on Infant Problem Solving: A Norwegian Prospective Observation Study. Nutrients 2018; DOI: 10.3390/nu10050529.
  • 154 Gould JF, Makrides M, Colombo J. et al. Randomized controlled trial of maternal omega-3 long-chain PUFA supplementation during pregnancy and early childhood development of attention, working memory, and inhibitory control. Am J Clin Nutr 2014; 99: 851-859
  • 155 Meldrum S, Dunstan JA, Foster JK. et al. Maternal fish oil supplementation in pregnancy: a 12 year follow-up of a randomised controlled trial. Nutrients 2015; 7: 2061-2067
  • 156 Bischoff-Ferrari HA. Vitamin D: role in pregnancy and early childhood. Ann Nutr Metab 2011; 59: 17-21
  • 157 Dawodu A, Wagner CL. Prevention of vitamin D deficiency in mothers and infants worldwide – a paradigm shift. Paediatr Int Child Health 2012; 32: 3-13
  • 158 Hyppönen E. Preventing vitamin D deficiency in pregnancy: importance for the mother and child. Ann Nutr Metab 2011; 59: 28-31
  • 159 Allerberger F, Wagner M. Listeriosis: a resurgent foodborne infection. Clin Microbiol Infect 2010; 16: 16-23
  • 160 Elsheikha HM. Congenital toxoplasmosis: priorities for further health promotion action. Public Health 2008; 122: 335-353
  • 161 Bundeszentrum für Ernährung. Listeriose und Toxoplasmose. Sicher essen in der Schwangerschaft. Bestell-Nr. 0346. Online: http://www.ble-medienservice.de last access: 31.07.2018
  • 162 Robert Koch-Institut. Infektionsepidemiologisches Jahrbuch meldepflichtiger Krankheiten für 2016. Berlin: Robert Koch-Institut; 2017
  • 163 Schoneberg I. Seltene Infektionskrankheiten in Deutschland. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2008; 51: 539-546
  • 164 Wilking H, Thamm M, Stark K. et al. Prevalence, incidence estimations, and risk factors of Toxoplasma gondii infection in Germany: a representative, cross-sectional, serological study. Sci Rep 2016; 6: 22551
  • 165 EFSA. Scientific Opinion of the Panel on Biological Hazards on a Request of EFSA on Surveillance and monitoring of Toxoplasma in humans, food and animals. EFSA Journal 2007; 583: 1-64
  • 166 Bojar I, Szymanska J. Environmental exposure of pregnant women to infection with Toxoplasma gondii–state of the art. Ann Agric Environ Med 2010; 17: 209-214
  • 167 Lamont RF, Sobel J, Mazaki-Tovi S. et al. Listeriosis in human pregnancy: a systematic review. J Perinat Med 2011; 39: 227-236
  • 168 Oliveira M, Usall J, Solsona C. et al. Effects of packaging type and storage temperature on the growth of foodborne pathogens on shredded ‘Romaine’ lettuce. Food Microbiol 2010; 27: 375-380
  • 169 Sinigaglia M, Bevilacqua A, Campaniello D. et al. Growth of Listeria monocytogenes in fresh-cut coconut as affected by storage conditions and inoculum size. Food Prot 2006; 69: 6
  • 170 Thevenot D, Delignette-Muller ML, Christieans S. et al. Prevalence of Listeria monocytogenes in 13 dried sausage processing plants and their products. Int J Food Microbiol 2005; 102: 85-94
  • 171 Evenson KR, Barakat R, Brown WJ. et al. Guidelines for Physical Activity during Pregnancy: Comparisons From Around the World. Am J Lifestyle Med 2014; 8: 102-121
  • 172 Pfeifer K, Banzer W, Ferrari N. et al. Nationale Empfehlungen für Bewegung und Bewegungsförderung. Köln: Bundeszentrale für gesundheitliche Aufklärung; 2017
  • 173 [Anonym] ACOG Committee Opinion No. 650: Physical Activity and Exercise During Pregnancy and the Postpartum Period. Obstet Gynecol 2015; 126: e135-e142
  • 174 National Institute for Health and Clinical Excellence. Antenatal care for uncomplicated pregnancies. Clinical guideline. Online: https://www.nice.org.uk/guidance/cg62/resources/antenatal-care-for-uncomplicated-pregnancies-pdf-975564597445 last access: 11.07.2107
  • 175 Colberg SR, Sigal RJ, Yardley JE. et al. Physical Activity/Exercise and Diabetes: A Position Statement of the American Diabetes Association. Diabetes Care 2016; 39: 2065-2079
  • 176 Di Mascio D, Magro-Malosso ER, Saccone G. et al. Exercise during pregnancy in normal-weight women and risk of preterm birth: a systematic review and meta-analysis of randomized controlled trials. Am J Obstet Gynecol 2016; 215: 561-571
  • 177 Magro-Malosso ER, Saccone G, Di Mascio D. et al. Exercise during pregnancy and risk of preterm birth in overweight and obese women: a systematic review and meta-analysis of randomized controlled trials. Acta Obstet Gynecol Scand 2017; 96: 263-273
  • 178 da Silva SG, Ricardo LI, Evenson KR. et al. Leisure-Time Physical Activity in Pregnancy and Maternal-Child Health: A Systematic Review and Meta-Analysis of Randomized Controlled Trials and Cohort Studies. Sports Med 2017; 47: 295-317
  • 179 Wiebe HW, Boule NG, Chari R. et al. The effect of supervised prenatal exercise on fetal growth: a meta-analysis. Obstet Gynecol 2015; 125: 1185-1194
  • 180 Aune D, Schlesinger S, Henriksen T. et al. Physical activity and the risk of preterm birth: a systematic review and meta-analysis of epidemiological studies. BJOG 2017; 124: 1816-1826
  • 181 Wen J, Xun P, Chen C. et al. Non-occupational physical activity during pregnancy and the risk of preterm birth: a meta-analysis of observational and interventional studies. Sci Rep 2017; 7: 44842
  • 182 Poyatos-Leon R, Garcia-Hermoso A, Sanabria-Martinez G. et al. Effects of exercise during pregnancy on mode of delivery: a meta-analysis. Acta Obstet Gynecol Scand 2015; 94: 1039-1047
  • 183 Magro-Malosso ER, Saccone G, Di Tommaso M. et al. Exercise during pregnancy and risk of gestational hypertensive disorders: a systematic review and meta-analysis. Acta Obstet Gynecol Scand 2017; 96: 921-931
  • 184 Yu Y, Xie R, Shen C. et al. Effect of exercise during pregnancy to prevent gestational diabetes mellitus: a systematic review and meta-analysis. J Matern Fetal Neonatal Med 2018; 31: 1632-1637
  • 185 Muktabhant B, Lawrie TA, Lumbiganon P. et al. Diet or exercise, or both, for preventing excessive weight gain in pregnancy. Cochrane Database Syst Rev 2015; (06) CD007145 DOI: 10.1002/14651858.CD007145.pub3.
  • 186 Yeo S, Walker JS, Caughey MC. et al. What characteristics of nutrition and physical activity interventions are key to effectively reducing weight gain in obese or overweight pregnant women? A systematic review and meta-analysis. Obes Rev 2017; 18: 385-399
  • 187 Perales M, Artal R, Lucia A. Exercise During Pregnancy. JAMA 2017; 317: 1113-1114
  • 188 Woodley SJ, Boyle R, Cody JD. et al. Pelvic floor muscle training for prevention and treatment of urinary and faecal incontinence in antenatal and postnatal women. Cochrane Database Syst Rev 2017; (12) CD007471
  • 189 Liddle SD, Pennick V. Interventions for preventing and treating low-back and pelvic pain during pregnancy. Cochrane Database Syst Rev 2015; (09) CD001139 DOI: 10.1002/14651858.CD001139.pub4.
  • 190 Shiri R, Coggon D, Falah-Hassani K. Exercise for the Prevention of Low Back Pain: Systematic Review and Meta-Analysis of Controlled Trials. Am J Epidemiol 2018; 187: 1093-1101
  • 191 World Health Organization. Global recommendations on physical activity for health. Genf: World Health Organization; 2010
  • 192 2018 Physical Activity Guidelines Advisory Committee. 2018 Physical Activity Guidelines Advisory Committee Scientific Report. Washington, DC: U.S. Department of Health and Human Services; 2018
  • 193 The American College of Obstetricians and Gynecologists, Committee on Obstetric Practice. Physical Activity and Exercise During Pregnancy and the Postpartum Period. Obstet Gynecol 2015; 126: e135-e142
  • 194 Mottola MF. Physical activity and maternal obesity: cardiovascular adaptations, exercise recommendations, and pregnancy outcomes. Nutr Rev 2013; 71 (Suppl. 01) S31-S36
  • 195 Tudor-Locke C, Craig CL, Brown WJ. et al. How many steps/day are enough? For adults. Int J Behav Nutr Phys Act 2011; 8: 79
  • 196 Baumann H, Bung P, Fallenstein F. et al. Reaction of mother and fetus to physical stress at high altitude. Geburtshilfe Frauenheilkd 1985; 45: 869-876
  • 197 Huch R. Physical activity at altitude in pregnancy. Semin Perinatol 1996; 20: 303-314
  • 198 Bo K, Artal R, Barakat R. et al. Exercise and pregnancy in recreational and elite athletes: 2016 evidence summary from the IOC expert group meeting, Lausanne. Part 1–exercise in women planning pregnancy and those who are pregnant. Br J Sports Med 2016; 50: 571-589
  • 199 Bo K, Artal R, Barakat R. et al. Exercise and pregnancy in recreational and elite athletes: 2016 evidence summary from the IOC expert group meeting, Lausanne. Part 2–the effect of exercise on the fetus, labour and birth. Br J Sports Med 2016; DOI: 10.1136/bjsports-2016-096810.
  • 200 Coll CV, Domingues MR, Goncalves H. et al. Perceived barriers to leisure-time physical activity during pregnancy: A literature review of quantitative and qualitative evidence. J Sci Med Sport 2017; 20: 17-25
  • 201 Brust JC. Ethanol and cognition: indirect effects, neurotoxicity and neuroprotection: a review. Int J Environ Res Public Health 2010; 7: 1540-1557
  • 202 Dolan GP, Stone DH, Briggs AH. A systematic review of continuous performance task research in children prenatally exposed to alcohol. Alcohol Alcohol 2010; 45: 30-38
  • 203 Spohr HL, Steinhausen HC. Fetal alcohol spectrum disorders and their persisting sequelae in adult life. Deutsches Arzteblatt international 2008; 105: 693-698
  • 204 Flak AL, Su S, Bertrand J. et al. The association of mild, moderate, and binge prenatal alcohol exposure and child neuropsychological outcomes: a meta-analysis. Alcohol Clin Exp Res 2014; 38: 214-226
  • 205 European Board and College of Obstetrics & Gynaecology. Position Statement from the European Board and College of Obstetrics & Gynaecology (EBCOG): Alcohol and pregnancy. Online: https://www.ebcog.org/blank-2/2015/11/27/EBCOG-Position-paper-on-Alcohol-and-pregnancy last access: 22.01.2018
  • 206 Shawe J, Delbaere I, Ekstrand M. et al. Preconception care policy, guidelines, recommendations and services across six European countries: Belgium (Flanders), Denmark, Italy, the Netherlands, Sweden and the United Kingdom. Eur J Contracept Reprod Health Care 2015; 20: 77-87
  • 207 Van Heertum K, Rossi B. Alcohol and fertility: how much is too much?. Fertil Res Pract 2017; 3: 10
  • 208 Niclasen J. Drinking or not drinking in pregnancy: the multiplicity of confounding influences. Alcohol Alcohol 2014; 49: 349-355
  • 209 Kesmodel US, Bertrand J, Stovring H. et al. The effect of different alcohol drinking patterns in early to mid pregnancy on the childʼs intelligence, attention, and executive function. BJOG 2012; 119: 1180-1190
  • 210 Leonardi-Bee J, Smyth A, Britton J. et al. Environmental tobacco smoke and fetal health: systematic review and meta-analysis. Arch Dis Child Fetal Neonatal Ed 2008; 93: F351-F361
  • 211 Murin S, Rafii R, Bilello K. Smoking and smoking cessation in pregnancy. Clin Chest Med 2011; 32: 75-91 viii
  • 212 Rebhan B, Kohlhuber M, Schwegler U. et al. Rauchen, Alkohol und Koffeinkonsum von Müttern vor, während und nach der Schwangerschaft – Ergebnisse der Studie „Stillverhalten in Bayern“. Gesundheitswesen 2009; 71: 391-398
  • 213 Reeves S, Bernstein I. Effects of maternal tobacco-smoke exposure on fetal growth and neonatal size. Expert Rev Obstet Gynecol 2008; 3: 719-730
  • 214 Schneider S, Maul H, Freerksen N. et al. Who smokes during pregnancy? An analysis of the German Perinatal Quality Survey 2005. Public Health 2008; 122: 1210-1216
  • 215 Mei-Dan E, Walfisch A, Weisz B. et al. The unborn smoker: association between smoking during pregnancy and adverse perinatal outcomes. J Perinat Med 2015; 43: 553-558
  • 216 Abraham M, Alramadhan S, Iniguez C. et al. A systematic review of maternal smoking during pregnancy and fetal measurements with meta-analysis. PLoS One 2017; 12: e0170946
  • 217 Pereira PP, Da Mata FA, Figueiredo AC. et al. Maternal Active Smoking During Pregnancy and Low Birth Weight in the Americas: A Systematic Review and Meta-analysis. Nicotine Tob Res 2017; 19: 497-505
  • 218 Bundeszentrale für gesundheitliche Aufklärung. Ich bekomme ein Baby. Rauchfrei in der Schwangerschaft. Ratgeber für Schwangere und ihre Partner. Köln: Bundeszentrale für gesundheitliche Aufklärung.
  • 219 Krebsforschungszentrum D. Tabakatlas Deutschland 2015 – Zahlen und Fakten. Online: https://www.dkfz.de/de/tabakkontrolle/download/Publikationen/sonstVeroeffentlichungen/Tabakatlas_auf_einen_Blick-Zahlen_und_Fakten.pdf last access: 29.12.2017
  • 220 Kuntz B, Zeiher J, Starker A. et al. Rauchen in der Schwangerschaft – Querschnittsergebnisse aus KiGGS Welle 2 und Trends. Journal of Health Monitoring 2018; 3: 47-54
  • 221 Bundesinstitut für Risikobewertung. Gesundheitliche Bewertung von Zusatzstoffen für Tabakerzeugnisse und elektronische Zigaretten. Stellungnahme Nr. 045/2015 vom 30. Juli 2015. 2015.
  • 222 CARE Study Group. Maternal caffeine intake during pregnancy and risk of fetal growth restriction: a large prospective observational study. BMJ 2008; 337: a2332
  • 223 Sengpiel V, Elind E, Bacelis J. et al. Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study. BMC Med 2013; 11: 42
  • 224 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies). Scientific Opinion on the safety of caffeine. EFSA Journal 2015; 13: 4102
  • 225 Lyngso J, Ramlau-Hansen CH, Bay B. et al. Association between coffee or caffeine consumption and fecundity and fertility: a systematic review and dose-response meta-analysis. Clin Epidemiol 2017; 9: 699-719
  • 226 Li J, Zhao H, Song JM. et al. A meta-analysis of risk of pregnancy loss and caffeine and coffee consumption during pregnancy. Int J Gynaecol Obstet 2015; 130: 116-122
  • 227 Jahanfar S, Jaafar SH. Effects of restricted caffeine intake by mother on fetal, neonatal and pregnancy outcomes. Cochrane Database Syst Rev 2015; (06) CD006965 DOI: 10.1002/14651858.CD006965.pub4.
  • 228 [Anonym] Fruchtsaft- und Erfrischungsgetränkeverordnung vom 24. Mai 2004 (BGBl. I S. 1016), die zuletzt durch Artikel 12 der Verordnung vom 5. Juli 2017 (BGBl. I S. 2272) geändert worden ist. Online: https://www.gesetze-im-internet.de/frsaftv_2004/BJNR101600004.html last access 24.07.2018
  • 229 Europäisches Parlament und Rat. Verordnung (EU) Nr. 1169/2011 des europäischen Parlaments und des Rates vom 25. Oktober 2011 betreffend die Information der Verbraucher über Lebensmittel und zur Änderung der Verordnungen (EG) Nr. 1924/2006 und (EG) Nr. 1925/2006 des Europäischen Parlaments und des Rates und zur Aufhebung der Richtlinie 87/250/EWG der Kommission, der Richtlinie 90/496/EWG des Rates, der Richtlinie 1999/10/EG der Kommission, der Richtlinie 2000/13/EG des Europäischen Parlaments und des Rates, der Richtlinien 2002/67/EG und 2008/5/EG der Kommission und der Verordnung (EG) Nr. 608/2004 der Kommission. Amtsbl Europäische Union 2011; L304/18.
  • 230 Bundesinstitut für Risikobewertung. Fragen und Antworten zu Koffein und koffeinhaltigen Lebensmitteln, einschließlich Energy Drinks. Online: https://www.bfr.bund.de/de/fragen_und_antworten_zu_koffein_und_koffeinhaltigen_lebensmitteln__einschliesslich_energy_drinks-194760.html last access: 24.07.2018
  • 231 Renfrew MJ, McCormick FM, Wade A. et al. Support for healthy breastfeeding mothers with healthy term babies. Cochrane Database Syst Rev 2012; (05) CD001141
  • 232 Kohlhuber M, Rebhan B, Schwegler U. et al. Breastfeeding rates and duration in Germany: a Bavarian cohort study. Br J Nutr 2008; 99: 1127-1132
  • 233 Rebhan B, Kohlhuber M, Schwegler U. et al. Infant feeding practices and associated factors through the first 9 months of life in Bavaria, Germany. J Pediatr Gastroenterol Nutr 2009; 49: 467-473
  • 234 Scott JA, Binns CW, Oddy WH. et al. Predictors of breastfeeding duration: evidence from a cohort study. Pediatrics 2006; 117: e646-e655
  • 235 Brown CR, Dodds L, Legge A. et al. Factors influencing the reasons why mothers stop breastfeeding. Can J Public Health 2014; 105: e179-e185
  • 236 Odom EC, Li R, Scanlon KS. et al. Reasons for earlier than desired cessation of breastfeeding. Pediatrics 2013; 131: e726-e732
  • 237 Rasenack R, Schneider C, Jahnz E. et al. Factors Associated with the Duration of Breastfeeding in the Freiburg Birth Collective, Germany (FreiStill). Geburtshilfe Frauenheilkd 2012; 72: 64-69
  • 238 Ayton J, van der Mei I, Wills K. et al. Cumulative risks and cessation of exclusive breast feeding: Australian cross-sectional survey. Arch Dis Child 2015; 100: 863-868
  • 239 Nationale Stillkommission am Bundesinstitut für Risikobewertung. Stillinformationen für Schwangere. Online: https://www.bfr.bund.de/cm/350/stillempfehlungen-fuer-schwangere-deutsch.pdf last access: 31.07.2018
  • 240 Skouteris H, Nagle C, Fowler M. et al. Interventions designed to promote exclusive breastfeeding in high-income countries: a systematic review. Breastfeed Med 2014; 9: 113-127
  • 241 McFadden A, Gavine A, Renfrew MJ. et al. Support for healthy breastfeeding mothers with healthy term babies. Cochrane Database Syst Rev 2017; (02) CD001141
  • 242 Dyson L, McCormick F, Renfrew MJ. Interventions for promoting the initiation of breastfeeding. Cochrane Database Syst Rev 2005; (02) CD001688 DOI: 10.1002/14651858.CD001688.pub2.
  • 243 Lumbiganon P, Martis R, Laopaiboon M. et al. Antenatal breastfeeding education for increasing breastfeeding duration. Cochrane Database Syst Rev 2016; (12) CD006425
  • 244 Balogun OO, OʼSullivan EJ, McFadden A. et al. Interventions for promoting the initiation of breastfeeding. Cochrane Database Syst Rev 2016; (11) CD001688
  • 245 Hannula L, Kaunonen M, Tarkka MT. A systematic review of professional support interventions for breastfeeding. J Clin Nurs 2008; 17: 1132-1143
  • 246 Sinha B, Chowdhury R, Sankar MJ. et al. Interventions to improve breastfeeding outcomes: a systematic review and meta-analysis. Acta Paediatr Suppl 2015; 104: 114-134
  • 247 Schäfer T, Bauer CP, Beyer K. et al. S3-Leitlinie Allergieprävention – Update 2014. Online: http://www.awmf.org/uploads/tx_szleitlinien/061-016l_S3_Allergiepr%25C3%25A4vention_2014-07.pdf last access: 02.08.2016
  • 248 Kramer MS, Kakuma R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Evid Based Child Health 2014; 9: 447-483
  • 249 Kramer MS, Kakuma R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Cochrane Database Syst Rev 2012; (09) CD000133 DOI: 10.1002/14651858.CD000133.pub3.
  • 250 Miles EA, Calder PC. Can Early Omega-3 Fatty Acid Exposure Reduce Risk of Childhood Allergic Disease?. Nutrients 2017; DOI: 10.3390/nu9070784.
  • 251 Gunaratne AW, Makrides M, Collins CT. Maternal prenatal and/or postnatal n-3 long chain polyunsaturated fatty acids (LCPUFA) supplementation for preventing allergies in early childhood. Cochrane Database Syst Rev 2015; (07) CD010085 DOI: 10.1002/14651858.CD010085.pub2.
  • 252 Bisgaard H, Stokholm J, Chawes BL. et al. Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring. N Engl J Med 2016; 375: 2530-2539
  • 253 Hansen S, Strom M, Maslova E. et al. Fish oil supplementation during pregnancy and allergic respiratory disease in the adult offspring. J Allergy Clin Immunol 2017; 139: 104-111.e4
  • 254 Deutsche Gesellschaft für Zahnerhaltung (DGZ), Deutsche Gesellschaft für Zahn-, Mund- und Kieferheilkunde, Deutsche Gesellschaft für Kinderzahnheilkunde (DGKiZ). et al. S2k-Leitlinie: Kariesprophylaxe bei bleibenden Zähnen – grundlegende Empfehlungen. Online: http://www.awmf.org/leitlinien/detail/ll/083-021.html last access: 27.12.2017
  • 255 Public Health Agency of Canada. Preconception Care. In: Public Health Agency of Canada, Family-Centred Maternity and Newborn Care: National Guidelines. Ottawa: Public Health Agency of Canada; 2017
  • 256 American Academy of Pediatric Dentistry (AAPD). Guideline on Perinatal Oral Health Care. Online: http://www.aapd.org/media/policies_guidelines/g_perinataloralhealthcare.pdf last access: 25.07.2018
  • 257 Lopez NJ, Uribe S, Martinez B. Effect of periodontal treatment on preterm birth rate: a systematic review of meta-analyses. Periodontol 2000 2015; 67: 87-130
  • 258 Iheozor-Ejiofor Z, Middleton P, Esposito M. et al. Treating periodontal disease for preventing adverse birth outcomes in pregnant women. Cochrane Database Syst Rev 2017; (06) CD005297
  • 259 da Silva Bastos Vde A, Freitas-Fernandes LB, Fidalgo TK. et al. Mother-to-child transmission of Streptococcus mutans: a systematic review and meta-analysis. J Dent 2015; 43: 181-191
  • 260 Chaffee BW, Gansky SA, Weintraub JA. et al. Maternal oral bacterial levels predict early childhood caries development. J Dent Res 2014; 93: 238-244
  • 261 Kohler B, Andreen I. Mutans streptococci and caries prevalence in children after early maternal caries prevention: a follow-up at 19 years of age. Caries Res 2012; 46: 474-480
  • 262 Meyer K, Khorshidi-Bohm M, Geurtsen W. et al. An early oral health care program starting during pregnancy–a long-term study–phase V. Clin Oral Investig 2014; 18: 863-872
  • 263 Raffauf AB, Kunze M, Ratka-Krüger P. Parodontale Behandlung während der Schwangerschaft. Wissenschaftliche Mitteilung der Deutschen Gesellschaft für Parodontologie (DGParo). Online: http://www.dgzmk.de/uploads/tx_szdgzmkdocuments/WM_PA-Schwangerschaft.pdf last access: 23.04.2018;
  • 264 Schwendicke F, Karimbux N, Allareddy V. et al. Periodontal treatment for preventing adverse pregnancy outcomes: a meta- and trial sequential analysis. PLoS One 2015; 10: e0129060
  • 265 American Dental Association (ADA), ADA Science Institute. Floss/Interdental Cleaners. Online: https://www.ada.org/en/member-center/oral-health-topics/floss last access: 19.05.2018
  • 266 Bundeszahnärztekammer (BZÄK), Deutsche Gesellschaft für Zahn-, Mund- und Kieferheilkunde. Wissenschaftlich abgesicherte Patienteninformation: Professionelle Zahnreinigung (PZR). Online: https://www.bzaek.de/fileadmin/PDFs/pati/bzaekdgzmk/2_03_pzr.pdf last access: 24.04.2017
  • 267 American Dental Association (ADA), ADA Science Institute. Pregnancy. Online : https://www.ada.org/en/member-center/oral-health-topics/pregnancy last access: 19.05.2018
  • 268 Europäisches Parlament und Europäischer Rat. Verordnung (EU) 2017/852 des Europäischen Parlaments und des Rates vom 17. Mai 2017 über Quecksilber und zur Aufhebung der Verordnung (EG) Nr. 1102/2008. Online: http://data.europa.eu/eli/reg/2017/852/oj last access: 19.05.2018
  • 269 Ständige Impfkommission am Robert Koch-Institut (RKI). Empfehlungen der Ständigen Impfkommission (STIKO) am Robert Koch-Institut – 2017/2018. Epidemiologisches Bulletin 2017; 34: 335-371
  • 270 Robert Koch-Institut. Impfen: Häufig gestellte Fragen und Antworten. Kann in der Schwangerschaft und Stillzeit geimpft werden?. Online: https://www.rki.de/SharedDocs/FAQ/Impfen/AllgFr_Allgemeine%20Fragen/FAQ-Liste_AllgFr_Impfen.html%23FAQId3400682 last access: 25.07.2018
  • 271 Ständige Impfkommission (STIKO) am Robert Koch-Institut. Änderung der Empfehlungen zur Impfung gegen Influenza. Epidemiologisches Bulletin 2010; 31: 299-309
  • 272 Shakib JH, Korgenski K, Presson AP. et al. . Pediatrics 2016; DOI: 10.1542/peds.2015-2360.

Correspondence/Korrespondenzadresse

Prof. Dr. Berthold Koletzko
LMU – Ludwig-Maximilians-Universität München
Dr. von Haunersches Kinderspital
Lindwurmstr. 4
80337 München
Germany   

 

Maria Flothkötter
Netzwerk Gesund ins Leben im Bundeszentrum für Ernährung (BZfE) in der Bundesanstalt für Landwirtschaft und Ernährung (BLE)
Deichmanns Aue 29
53179 Bonn
Germany   

  • References/Literatur

  • 1 Koletzko B, Schiess S, Brands B. et al. [Infant feeding practice and later obesity risk. Indications for early metabolic programming]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2010; 53: 666-673
  • 2 Bundesministerium für Gesundheit. Nationales Gesundheitsziel – Gesundheit rund um die Geburt. Online: https://www.bundesregierung.de/Content/Infomaterial/BMG/_3005.html?view=trackDownload last access: 31.07.2018
  • 3 Röbl-Mathieu M. Preconception Counselling. Frauenarzt 2013; 54: 966-972
  • 4 Hanson MA, Bardsley A, De-Regil LM. et al. The International Federation of Gynecology and Obstetrics (FIGO) recommendations on adolescent, preconception, and maternal nutrition: “Think Nutrition First”. Int J Gynaecol Obstet 2015; 131 (Suppl. 04) S213-S253
  • 5 Mensink GBM, Schienkiewitz A, Haftenberger M. et al. Übergewicht und Adipositas in Deutschland. Ergebnisse der Studie zur Gesundheit Erwachsener in Deutschland (DEGS1). Bundesgesundheitsbl 2013; 56: 786-794
  • 6 Stubert J, Reister F, Hartmann S. et al. Risiken bei Adipositas in der Schwangerschaft. Dtsch Arztebl Int 2018; 115: 276-282
  • 7 Davies SC. Annual Report of the Chief Medical Officer, 2014, The Health of the 51 %: Women. London: Department of Health; 2015
  • 8 Melchior H, Kurch-Bek D, Mund J. The prevalence of gestational diabetes. Dtsch Arztebl Int 2017; 114: 412-418
  • 9 Schoenaker DA, Mishra GD, Callaway LK. et al. The Role of Energy, Nutrients, Foods, and Dietary Patterns in the Development of Gestational Diabetes Mellitus: A Systematic Review of Observational Studies. Diabetes Care 2016; 39: 16-23
  • 10 Bennett CJ, Walker RE, Blumfield ML. et al. Interventions designed to reduce excessive gestational weight gain can reduce the incidence of gestational diabetes mellitus: A systematic review and meta-analysis of randomised controlled trials. Diabetes Res Clin Pract 2018; 141: 69-79
  • 11 Orth B, Töppich J. Rauchen bei Jugendlichen und jungen Erwachsenen in Deutschland 2014. Ergebnisse einer aktuellen Repräsentativbefragung und Trends. Online: https://www.bzga.de/forschung/studien-untersuchungen/studien/suchtpraevention/?sub=90 last access: 29.12.2017
  • 12 Die Drogenbeauftragte der Bundesregierung Bundesministerium für Gesundheit. Hrsg. Drogen- und Suchtbericht Juni 2016. Online: https://www.drogenbeauftragte.de/fileadmin/dateien-dba/Drogenbeauftragte/4_Presse/1_Pressemitteilungen/2016/2016_2/160928_Drogenbericht-2016_NEU_Sept.2016.pdf last access: 31.07.2018
  • 13 Koletzko B, Bauer CP, Bung P. et al. [Nutrition in pregnancy – Practice recommendations of the Network „Healthy Start – Young Family Network“]. Dtsch Med Wochenschr 2012; 137: 1366-1372
  • 14 Stephenson J, Heslehurst N, Hall J. et al. Before the beginning: nutrition and lifestyle in the preconception period and its importance for future health. Lancet 2018; 391: 1830-1841
  • 15 Bundeszentrale für gesundheitliche Aufklärung. frauen leben 3. Familienplanung im Leben von Frauen. Schwerpunkt: Ungewollte Schwangerschaften. Köln: Bundeszentrale für gesundheitliche Aufklärung; 2016
  • 16 Zhang C, Wu Y, Li S. et al. Maternal prepregnancy obesity and the risk of shoulder dystocia: a meta-analysis. BJOG 2017; DOI: 10.1111/1471-0528.14841.
  • 17 Balsells M, Garcia-Patterson A, Corcoy R. Systematic review and meta-analysis on the association of prepregnancy underweight and miscarriage. Eur J Obstet Gynecol Reprod Biol 2016; 207: 73-79
  • 18 Meehan S, Beck CR, Mair-Jenkins J. et al. Maternal obesity and infant mortality: a meta-analysis. Pediatrics 2014; 133: 863-871
  • 19 World Health Organization Regional Office for Europe. Good maternal Nutrition. The best Start in Life. Copenhagen, Denmark: WHO Regional Office for Europe; 2016
  • 20 Gaudet L, Ferraro ZM, Wen SW. et al. Maternal obesity and occurrence of fetal macrosomia: a systematic review and meta-analysis. Biomed Res Int 2014; 2014: 640291
  • 21 OʼConnor DL, Blake J, Bell R. et al. Nutrition Working Group. Canadian Consensus on Female Nutrition: Adolescence, Reproduction, Menopause, and Beyond. J Obstet Gynaecol Can 2016; 38: 508-554.e18
  • 22 National Institute for Health and Clinical Excellence. Weight management before, during and after pregnancy. Online: https://www.nice.org.uk/guidance/ph27/resources/weight-management-before-during-and-after-pregnancy-pdf-1996242046405 last access: 16.11.2017
  • 23 Dudenhausen JW, Grunebaum A, Kirschner W. Prepregnancy body weight and gestational weight gain-recommendations and reality in the USA and in Germany. Am J Obstet Gynecol 2015; 213: 591-592
  • 24 Beyerlein A, Lack N, von Kries R. Within-population average ranges compared with Institute of Medicine recommendations for gestational weight gain. Obstet Gynecol 2010; 116: 1111-1118
  • 25 World Health Organization, Food and Agriculture Organization of the United Nations, University UN. Human energy requirements. Report of a Joint FAO/WHO/UNU Expert Consultation, Rome, Italy, 17 – 24 October 2001. Rome: WHO; 2004
  • 26 Goldberg GR. Nutrition in pregnancy: the facts and fallacies. Nurs Stand 2003; 17: 39-42
  • 27 Rasmussen KM, Yaktin AL. Committee to reexamine IOM Pregnancy Weight Guidelines. Weight Gain during Pregnancy: reexamining the Guidelines. Washington (DC): Institute of Medicine (US) and National Research Council (US); 2009
  • 28 Goldstein RF, Abell SK, Ranasinha S. et al. Association of Gestational Weight Gain With Maternal and Infant Outcomes: A Systematic Review and Meta-analysis. JAMA 2017; 317: 2207-2225
  • 29 Margerison Zilko CE, Rehkopf D, Abrams B. Association of maternal gestational weight gain with short- and long-term maternal and child health outcomes. Am J Obstet Gynecol 2010; 202: 574.e1-574.e8
  • 30 Scott C, Andersen CT, Valdez N. et al. No global consensus: a cross-sectional survey of maternal weight policies. BMC Pregnancy Childbirth 2014; 14: 167
  • 31 Alavi N, Haley S, Chow K. et al. Comparison of national gestational weight gain guidelines and energy intake recommendations. Obes Rev 2013; 14: 68-85
  • 32 Blake-Lamb TL, Locks LM, Perkins ME. et al. Interventions for Childhood Obesity in the First 1,000 Days A Systematic Review. Am J Prev Med 2016; 50: 780-789
  • 33 Nicklas JM, Barbour LA. Optimizing Weight for Maternal and Infant Health – Tenable, or Too Late?. Expert Rev Endocrinol Metab 2015; 10: 227-242
  • 34 Boney CM, Verma A, Tucker R. et al. Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics 2005; 115: e290-e296
  • 35 Reynolds RM, Allan KM, Raja EA. et al. Maternal obesity during pregnancy and premature mortality from cardiovascular event in adult offspring: follow-up of 1 323 275 person years. BMJ 2013; 347: f4539
  • 36 Vinturache A, McKeating A, Daly N. et al. Maternal body mass index and the prevalence of spontaneous and elective preterm deliveries in an Irish obstetric population: a retrospective cohort study. BMJ Open 2017; 7: e015258
  • 37 Hoellen F, Hornemann A, Haertel C. et al. Does maternal underweight prior to conception influence pregnancy risks and outcome?. In Vivo 2014; 28: 1165-1170
  • 38 Shin D, Song WO. Prepregnancy body mass index is an independent risk factor for gestational hypertension, gestational diabetes, preterm labor, and small- and large-for-gestational-age infants. Matern Fetal Neonatal Med 2015; 28: 1679-1686
  • 39 Busetto L, Dicker D, Azran C. et al. Practical Recommendations of the Obesity Management Task Force of the European Association for the Study of Obesity for the Post-Bariatric Surgery Medical Management. Obes Facts 2017; 10: 597-632
  • 40 Deutsche Adipositas-Gesellschaft (DAG) e.V., Deutsche Diabetes Gesellschaft (DDG), Deutsche Gesellschaft für Ernährung (DGE) e.V.. et al Interdisziplinäre Leitlinie der Qualität S3 zur „Prävention und Therapie der Adipositas“. Online: http://www.adipositas-gesellschaft.de/fileadmin/PDF/Leitlinien/S3_Adipositas_Praevention_Therapie_2014.pdf last access: 28.05.2018
  • 41 Kwong W, Tomlinson G, Feig DS. Maternal and neonatal outcomes after bariatric surgery; a systematic review and meta-analysis: do the benefits outweigh the risks?. Am J Obstet Gynecol 2018; 218: 573-580
  • 42 Jaddoe VWV. Persönliche Mitteilung. 2018
  • 43 Beyerlein A, Schiessl B, Lack N. et al. Optimal gestational weight gain ranges for the avoidance of adverse birth weight outcomes: a novel approach. Am J Clin Nutr 2009; 90: 1552-1558
  • 44 Rogozinska E, Marlin N, Jackson L. et al. Effects of antenatal diet and physical activity on maternal and fetal outcomes: individual patient data meta-analysis and health economic evaluation. Health Technol Assess 2017; 21: 1-158
  • 45 Dodd JM, Turnbull D, McPhee AJ. et al. Antenatal lifestyle advice for women who are overweight or obese: LIMIT randomised trial. BMJ 2014; 348: g1285
  • 46 Poston L, Bell R, Croker H. et al. Effect of a behavioural intervention in obese pregnant women (the UPBEAT study): a multicentre, randomised controlled trial. Lancet Diabetes Endocrinol 2015; 3: 767-777
  • 47 International Weight Management in Pregnancy Collaborative Group. Effect of diet and physical activity based interventions in pregnancy on gestational weight gain and pregnancy outcomes: meta-analysis of individual participant data from randomised trials. BMJ 2017; 358: j3119
  • 48 Starling AP, Brinton JT, Glueck DH. et al. Associations of maternal BMI and gestational weight gain with neonatal adiposity in the Healthy Start study. Am J Clin Nutr 2015; 101: 302-309
  • 49 Tan HC, Roberts J, Catov J. et al. Motherʼs pre-pregnancy BMI is an important determinant of adverse cardiometabolic risk in childhood. Pediatr Diabetes 2015; 16: 419-426
  • 50 Plachta-Danielzik S, Kehden B, Landsberg B. et al. Attributable risks for childhood overweight: evidence for limited effectiveness of prevention. Pediatrics 2012; 130: e865-e871
  • 51 EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA). Scientific Opinion on Dietary Reference Values for energy. EFSA Journal 2013; 11: 3005
  • 52 Deutsche Gesellschaft für Ernährung (DGE); Österreichische Gesellschaft für Ernährung (ÖGE), Schweizerische Gesellschaft für Ernährung (SGE). Referenzwerte für die Nährstoffzufuhr. Bonn: 2017
  • 53 Ferrari N, Graf C. Bewegungsempfehlungen für Frauen während und nach der Schwangerschaft. Gesundheitswesen 2017; 79: S36-S39
  • 54 Cantwell R, Clutton-Brock T, Cooper G. et al. Saving Mothersʼ Lives: Reviewing maternal deaths to make motherhood safer: 2006–2008. The Eighth Report of the Confidential Enquiries into Maternal Deaths in the United Kingdom. BJOG 2011; 118 (Suppl. 01) 1-203
  • 55 Catalano PM. Obesity, insulin resistance, and pregnancy outcome. Reproduction 2010; 140: 365-371
  • 56 Rasmussen KM, Abrams B, Bodnar LM. et al. Recommendations for weight gain during pregnancy in the context of the obesity epidemic. Obstet Gynecol 2010; 116: 1191-1195
  • 57 Tielemans MJ, Garcia AH, Peralta Santos A. et al. Macronutrient composition and gestational weight gain: a systematic review. Am J Clin Nutr 2016; 103: 83-99
  • 58 FAO/WHO/UNU Expert Consultation. Human energy requirements: report of a joint FAO/WHO/UNU Expert Consultation. Food Nutr Bull 2005; 26: 166
  • 59 Lof M. Physical activity pattern and activity energy expenditure in healthy pregnant and non-pregnant Swedish women. Eur J Clin Nutr 2011; 65: 1295-1301
  • 60 Rauh K, Gabriel E, Kerschbaum E. et al. Safety and efficacy of a lifestyle intervention for pregnant women to prevent excessive maternal weight gain: a cluster-randomized controlled trial. BMC Pregnancy Childbirth 2013; 13: 151
  • 61 Berti C, Biesalski HK, Gartner R. et al. Micronutrients in pregnancy: current knowledge and unresolved questions. Clini Nutr 2011; 30: 689-701
  • 62 Forschungsinstitut für Kinderernährung. Hrsg. Empfehlungen für die Ernährung von Mutter und Kind. Dortmund: Forschungsinstitut für Kinderernährung; 2016
  • 63 Deutsche Gesellschaft für Ernährung. Vollwertig essen und trinken nach den 10 Regeln der DGE. Online: http://www.dge.de/ernaehrungspraxis/vollwertige-ernaehrung/10-regeln-der-dge/ last access: 20.11.2017
  • 64 The American Society for Reproductive Medicine. Optimizing natural fertility: a committee opinion. Practice Committee of the American Society for Reproductive Medicine in collaboration with the Society for Reproductive Endocrinology and Infertility. Fertil Steril 2013; 100: 631-637
  • 65 Poston L, Bell R, Briley AL. et al. Improving Pregnancy Outcome in obese Women: the UK Pregnancies Better Eating and Activity randomised controlled Trial. Southampton (UK): NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House; 2017
  • 66 Koletzko B, Brands B, Grote V. et al. Long-Term Health Impact of Early Nutrition: The Power of Programming. Ann Nutr Metab 2017; 70: 161-169
  • 67 Thangaratinam S, Rogozinska E, Jolly K. et al. Effects of interventions in pregnancy on maternal weight and obstetric outcomes: meta-analysis of randomised evidence. BMJ 2012; 344: e2088
  • 68 Harrison CL, Lombard CB, Strauss BJ. et al. Optimizing healthy gestational weight gain in women at high risk of gestational diabetes: a randomized controlled trial. Obesity 2013; 21: 904-909
  • 69 Zhang R, Han S, Chen GC. et al. Effects of low-glycemic-index diets in pregnancy on maternal and newborn outcomes in pregnant women: a meta-analysis of randomized controlled trials. Eur J Nutr 2018; 57: 167-177
  • 70 Deutsche Gesellschaft für Ernährung. Ausgewählte Fragen und Antworten zu Folat. Online: https://www.dge.de/wissenschaft/weitere-publikationen/faqs/folat/ last access: 24.07.2018
  • 71 EFSA Panel on Contaminants in the Food Chain. Opinion of the Scientific Panel on Contaminants in the Food Chain on a request from the Commission related to mercury and methylmercury in food. EFSA Journal 2004; 34: 1-14
  • 72 Piccoli GB, Clari R, Vigotti FN. et al. Vegan-vegetarian diets in pregnancy: danger or panacea? A systematic narrative review. BJOG 2015; 122: 623-633
  • 73 Richter M, Boeing H, Grünewald-Funk D. et al. Vegane Ernährung. Position der Deutschen Gesellschaft für Ernährung e. V. (DGE). Ernährungs Umschau 2016; 63: 92-102
  • 74 Dror DK, Allen LH. Effect of vitamin B12 deficiency on neurodevelopment in infants: current knowledge and possible mechanisms. Nutr Rev 2008; 66: 250-255
  • 75 Honzik T, Adamovicova M, Smolka V. et al. Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B12 deficiency–what have we learned?. Eur J Paediatr Neurol 2010; 14: 488-495
  • 76 von Schenck U, Bender-Gotze C, Koletzko B. Persistence of neurological damage induced by dietary vitamin B-12 deficiency in infancy. Arch Dis Child 1997; 77: 137-139
  • 77 Wada L, King JC. Trace element nutrition during pregnancy. Clin Obstet Gynecol 1994; 37: 574-586
  • 78 Wagener IE, Bergmann RL, Kamtsiuris P. et al. Prävalenz und Risikofaktoren für Eisenmangel bei jungen Müttern. Gesundheitswesen 2000; 62: 176-178
  • 79 King JC, Stein T, Doyle M. Effect of vegetarianism on the zinc status of pregnant women. Am J Clin Nutr 1981; 34: 1049-1055
  • 80 Koebnick C, Hoffmann I, Dagnelie PC. et al. Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women. J Nutr 2004; 134: 3319-3326
  • 81 Czeizel AE, Dudas I, Paput L. et al. Prevention of neural-tube defects with periconceptional folic acid, methylfolate, or multivitamins?. Ann Nutr Metab 2011; 58: 263-271
  • 82 De-Regil LM, Pena-Rosas JP, Fernandez-Gaxiola AC. et al. Effects and safety of periconceptional oral folate supplementation for preventing birth defects. Cochrane Database Syst Rev 2015; (12) CD007950 DOI: 10.1002/14651858.CD007950.pub3.
  • 83 Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 1992; 327: 1832-1835
  • 84 Viswanathan M, Treiman KA, Doto JK. et al. Folic Acid Supplementation: An Evidence Review for the U.S. Preventive Services Task Force. Rockville (MD): Agency for Healthcare Research and Quality (US); 2017
  • 85 [Anonym] Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet 1991; 338: 131-137
  • 86 Obeid R, Pietrzik K. Neuralrohrdefekte: Das Veto gegen Folsäure im Mehl sollte überdacht werden. Dtsch Arztebl 2018; 115 (27-28): A-1329/B-1123/C-1115
  • 87 Koletzko B, Pietrzik K. Gesundheitliche Bedeutung der Folsäurezufuhr. Dtsch Arztebl 2004; 101: A-1670/B-1388/C-1338
  • 88 Deutsche Gesellschaft für Ernährung, Deutsche Gesellschaft für Humangenetik, Deutsche Gesellschaft für Kinderheilkunde. et al. Prävention von Neuralrohrdefekten durch Folsäurezufuhr in der Frühschwangerschaft. Der Frauenarzt 1994; 35: 1007–1010. Nachdruck in: Der Kinderarzt 1995; 26: 187–190; .2: ASbH-Brief – Zeitschrift der Arbeitsgemeinschaft Spina bifida und Hydrocephalus e. V.; .3: 1995; 1995;. Monatsschr Kinderheilkd 1995; 143: 1003-1005
  • 89 Krawinkel MB, Strohm D, Weissenborn A. et al. Revised D-A-CH intake recommendations for folate: how much is needed?. Eur J Clin Nutr 2014; 68: 719-723
  • 90 Gomes S, Lopes C, Pinto E. Folate and folic acid in the periconceptional period: recommendations from official health organizations in thirty-six countries worldwide and WHO. Public Health Nutr 2016; 19: 176-189
  • 91 Australian Government Department of Health. Clinical Practice Guidelines: Pregnancy Care. Online: http://www.health.gov.au/internet/main/publishing.nsf/Content/pregnancycareguidelines last access: 26.07.2018
  • 92 Bramswig S, Prinz-Langenohl R, Lamers Y. et al. Supplementation with a multivitamin containing 800 microg of folic acid shortens the time to reach the preventive red blood cell folate concentration in healthy women. Int J Vitam Nutr Res 2009; 79: 61-70
  • 93 Obeid R, Schon C, Wilhelm M. et al. The effectiveness of daily supplementation with 400 or 800 microg/day folate in reaching protective red blood folate concentrations in non-pregnant women: a randomized trial. Eur J Nutr 2017; DOI: 10.1007/s00394-017-1461-8.
  • 94 World Health Organization. Guideline: Optimal Serum and Red Blood Cell Folate Concentrations in Women of reproductive Age for Prevention of neural Tube Defects. Geneva: WHO; 2015
  • 95 Max Rubner Institut. Nationale Verzehrsstudie II, Ergebnisbericht. Karlsruhe: Bundesforschungsinstitut für Ernährung und Lebensmittel; 2008
  • 96 Mensink G, Weißenborn A, Richter A. Ernährungssituation in Deutschland. Folat. In: Deutsche Gesellschaft für Ernährung. Hrsg. 13 DGE-Ernährungsbericht. Bonn: Deutsche Gesellschaft für Ernährung; 2016
  • 97 Pietrzik K, Lamers Y, Bramswig S. et al. Calculation of red blood cell folate steady state conditions and elimination kinetics after daily supplementation with various folate forms and doses in women of childbearing age. Am J Clin Nutr 2007; 86: 1414-1419
  • 98 Scientific Committee on Food, European Commission. Opinion of the Scientific Committee on Food on the tolerable upper intake level of folate. Brüssel: Europäische Kommission; 2000
  • 99 Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes and its Panel on Folate OBV, and Choline. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington (DC): National Academies Press (US) National Academy of Sciences; 1998
  • 100 Oliver EM, Grimshaw KE, Schoemaker AA. et al. Dietary habits and supplement use in relation to national pregnancy recommendations: data from the EuroPrevall birth cohort. Matern Child Health J 2014; 18: 2408-2425
  • 101 Egen V, Hasford J. Prevention of neural tube defects: effect of an intervention aimed at implementing the official recommendations. Sozial- und Praventivmedizin 2003; 48: 24-32
  • 102 Kowoll S, Kurzenhäuser-Carstens S, Martin A. et al. Folsäure zur Prävention von Neuralrohrdefekten – Wissen und Einstellungen sowie Beratungs- und Einnahmepraxis in Berlin. Z Geburtshilfe Neonatol 2015; DOI: 10.1055/s-005-30402.
  • 103 Becker S, Schmid D, Amann-Gassner U. et al. Verwendung von Nährstoffsupplementen vor und während der Schwangerschaft. Ernährungs Umschau 2011; 58: 36-41
  • 104 World Health Organization. Urinary iodine concentrations for determing iodine status in population. Online: http://apps.who.int/iris/bitstream/10665/85972/1/WHO_NMH_NHD_EPG_13.1_eng.pdf last access: 24.11.2017
  • 105 Deutsche Gesellschaft für Ernährung. Hrsg. 13. Ernährungsbericht. Bonn: Deutsche Gesellschaft für Ernährung; 2016
  • 106 Gemeinsamer Bundesausschuss. Richtlinien des Gemeinsamen Bundesausschusses über die ärztliche Betreuung während der Schwangerschaft und nach der Entbindung („Mutterschafts-Richtlinien“) in der Fassung vom 10. Dezember 1985 (veröffentlicht im Bundesanzeiger Nr. 60 a vom 27. März 1986), zuletzt geändert am 21. April 2016, veröffentlicht im Bundesanzeiger AT 19.07.2016 B5, in Kraft getreten am 20. Juli 2016. Bundesanzeiger 2016; AT 19.07.2016.
  • 107 Alexander EK, Pearce EN, Brent GA. et al. 2017 Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and the Postpartum. Thyroid 2017; 27: 315-389
  • 108 Australian Government National Health and Medical Research Council (NHMRC). NHMRC Public Statement: Iodine Supplementation for Pregnant and Breastfeeding Women. 2010. Online: https://www.nhmrc.gov.au/guidelines-publications/new45 last access: 24.11.2017
  • 109 Taylor PN, Vaidya B. Iodine supplementation in pregnancy – is it time?. Clin Endocrinol (Oxf) 2016; 85: 10-14
  • 110 EFSA NDA Panel (EFSA Panel on Panel on Dietetic Products Nutrition and Allergies). Scientific Opinion on Dietary Reference Values for iodine. EFSA Journal 2014; 12: 3660
  • 111 Bath SC, Steer CD, Golding J. et al. Effect of inadequate iodine status in UK pregnant women on cognitive outcomes in their children: results from the Avon Longitudinal Study of Parents and Children (ALSPAC). Lancet 2013; 382: 331-337
  • 112 Bougma K, Aboud FE, Harding KB. et al. Iodine and mental development of children 5 years old and under: a systematic review and meta-analysis. Nutrients 2013; 5: 1384-1416
  • 113 Rayman MP, Bath SC. The new emergence of iodine deficiency in the UK: consequences for child neurodevelopment. Ann Clin Biochem 2015; 52: 705-708
  • 114 Trumpff C, De Schepper J, Tafforeau J. et al. Mild iodine deficiency in pregnancy in Europe and its consequences for cognitive and psychomotor development of children: a review. J Trace Elem Med Biol 2013; 27: 174-183
  • 115 Ghassabian A, Henrichs J, Tiemeier H. Impact of mild thyroid hormone deficiency in pregnancy on cognitive function in children: lessons from the Generation R Study. Best Pract Res Clin Endocrinol Metab 2014; 28: 221-232
  • 116 Abel MH, Caspersen IH, Meltzer HM. et al. Suboptimal Maternal Iodine Intake Is Associated with Impaired Child Neurodevelopment at 3 Years of Age in the Norwegian Mother and Child Cohort Study. J Nutr 2017; 147: 1314-1324
  • 117 Redman K, Ruffman T, Fitzgerald P. et al. Iodine Deficiency and the Brain: Effects and Mechanisms. Crit Rev Food Sci Nutr 2016; 56: 2695-2713
  • 118 Taylor PN, Okosieme OE, Dayan CM. et al. Therapy of endocrine disease: Impact of iodine supplementation in mild-to-moderate iodine deficiency: systematic review and meta-analysis. Eur J Endocrinol 2014; 170: R1-R15
  • 119 Harding KB, Pena-Rosas JP, Webster AC. et al. Iodine supplementation for women during the preconception, pregnancy and postpartum period. Cochrane Database Syst Rev 2017; (03) CD011761
  • 120 Zhou SJ, Anderson AJ, Gibson RA. et al. Effect of iodine supplementation in pregnancy on child development and other clinical outcomes: a systematic review of randomized controlled trials. Am J Clin Nutr 2013; 98: 1241-1254
  • 121 Bundesinstitut für Risikobewertung. Gesundheitliche Risiken durch zu hohen Jodgehalt in getrockneten Algen. Aktualisierte Stellungnahme Nr. 026/2007 des BfR vom 22. Juni 2004, aktualisiert am 12. Juni 2007. 2007. Online: https://www.bfr.bund.de/cm/343/gesundheitliche_risiken_durch_zu_hohen_jodgehalt_in_getrockneten_algen.pdf last access: 24.11.2017
  • 122 Bouga M, Combet E. Emergence of Seaweed and Seaweed-Containing Foods in the UK: Focus on Labeling, Iodine Content, Toxicity and Nutrition. Foods (Basel, Switzerland) 2015; 4: 240-253
  • 123 Pena-Rosas JP, De-Regil LM, Garcia-Casal MN. et al. Daily oral iron supplementation during pregnancy. Cochrane Database Syst Rev 2015; (07) CD004736 DOI: 10.1002/14651858.CD004736.pub5.
  • 124 Vucic V, Berti C, Vollhardt C. et al. Effect of iron intervention on growth during gestation, infancy, childhood, and adolescence: a systematic review with meta-analysis. Nutr Rev 2013; 71: 386-401
  • 125 McDonagh M, Cantor A, Bougatsos C. et al. In: Routine Iron Supplementation and Screening for Iron Deficiency Anemia in Pregnant Women: A Systematic Review to Update the US Preventive Services Task Force Recommendation. Rockville (MD): Agency for Healthcare Research and Quality (US); 2015
  • 126 Milman N. Oral iron prophylaxis in pregnancy: not too little and not too much!. J Pregnancy 2012; 2012: 514345
  • 127 Hwang JY, Lee JY, Kim KN. et al. Maternal iron intake at mid-pregnancy is associated with reduced fetal growth: results from Mothers and Childrenʼs Environmental Health (MOCEH) study. Nutr J 2013; 12: 38
  • 128 NIHR Dissemination Centre. Better Beginnings. Improving Health for Pregnancy. Themed Review. Online: http://www.dc.nihr.ac.uk/themed-reviews/Better-beginnings-web-interactive.pdf last access: 23.01.2018
  • 129 Haute Autorité de Santé. Comment mieux informer les femmes enceintes?. Online: https://www.has-sante.fr/portail/jcms/c_268522/fr/information-femmes-enceintes-recommandations-pdf last access: 31.07.2018
  • 130 Institute of Obstetricians & Gynaecologists RCoPoI, Directorate of Clinical Strategy and Programmes, Health Service Executiv. Clinical Practice Guideline: Nutrition for Pregnancy. Online: https://rcpi-live-cdn.s3.amazonaws.com/wp-content/uploads/2016/05/22.-Nutrition-during-Pregnancy.pdf last access: 31.07.2018
  • 131 World Health Organization. Guideline: Intermittent Iron and Folic Acid Supplementation in Non-Anaemic Pregnant Women. Geneva: WHO; 2012
  • 132 EFSA Panel on Dietetic Products, Nutrition and Allergies. Scientific Opinion on Dietary Reference Values for fats, including saturated fatty acids, polyunsaturated fatty acids, monounsaturated fatty acids, trans fatty acids, and cholesterol. EFSA Journal 2010; DOI: 10.2903/j.efsa.2010.1461.
  • 133 Koletzko B, Lien E, Agostoni C. et al. The roles of long-chain polyunsaturated fatty acids in pregnancy, lactation and infancy: review of current knowledge and consensus recommendations. J Perinat Med 2008; 36: 5-14
  • 134 Menon KC, Ferguson EL, Thomson CD. et al. Effects of anemia at different stages of gestation on infant outcomes. Nutrition 2016; 32: 61-65
  • 135 Scholl TO, Hediger ML, Fischer RL. et al. Anemia vs. iron deficiency: increased risk of preterm delivery in a prospective study. Am J Clin Nutr 1992; 55: 985-988
  • 136 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA)). Scientific Opinion on Dietary Reference Values for iron. EFSA Journal 2015; 13: 4254
  • 137 Bergmann RL, Dudenhausen JW, Ennen JC. et al. Diagnostik und Behandlung der Anämie und des Eisenmangels in der Schwangerschaft und im Wochenbett. Geburtshilfe Frauenheilkd 2009; 69: 682-686
  • 138 Burdge GC, Tan SY, Henry CJ. Long-chain n-3 PUFA in vegetarian women: a metabolic perspective. J Nutr Sci 2017; 6: e58
  • 139 Glaser C, Lattka E, Rzehak P. et al. Genetic variation in polyunsaturated fatty acid metabolism and its potential relevance for human development and health. Matern Child Nutr 2011; 7 (Suppl. 02) 27-40
  • 140 Lattka E, Klopp N, Demmelmair H. et al. Genetic variations in polyunsaturated fatty acid meatbolism-implixations for child health?. Ann Nutr Metab 2012; 60: 8-17
  • 141 Koletzko B, Boey CC, Campoy C. et al. Current information and Asian perspectives on long-chain polyunsaturated fatty acids in pregnancy, lactation, and infancy: systematic review and practice recommendations from an early nutrition academy workshop. Ann Nutr Metab 2014; 65: 49-80
  • 142 Brenna JT. Efficiency of conversion of alpha-linolenic acid to long chain n-3 fatty acids in man. Curr Opin Clin Nutr Metab Care 2002; 5: 127-132
  • 143 Brenna JT, Salem jr. N, Sinclair AJ. et al. alpha-Linolenic acid supplementation and conversion to n-3 long-chain polyunsaturated fatty acids in humans. Prostaglandins Leukot Essent Fatty Acids 2009; 80: 85-91
  • 144 Barcelo-Coblijn G, Murphy EJ. Alpha-linolenic acid and its conversion to longer chain n-3 fatty acids: benefits for human health and a role in maintaining tissue n-3 fatty acid levels. Prog Lipid Res 2009; 48: 355-374
  • 145 Kar S, Wong M, Rogozinska E. et al. Effects of omega-3 fatty acids in prevention of early preterm delivery: a systematic review and meta-analysis of randomized studies. Eur J Obstet Gynecol Reprod Biol 2016; 198: 40-46
  • 146 Makrides M, Duley L, Olsen SF. Marine oil, and other prostaglandin precursor, supplementation for pregnancy uncomplicated by pre-eclampsia or intrauterine growth restriction. Cochrane Database Syst Rev 2006; (03) CD003402 DOI: 10.1002/14651858.CD003402.pub2.
  • 147 Yelland LN, Gajewski BJ, Colombo J. et al. Predicting the effect of maternal docosahexaenoic acid (DHA) supplementation to reduce early preterm birth in Australia and the United States using results of within country randomized controlled trials. Prostaglandins Leukot Essent Fatty Acids 2016; 112: 44-49
  • 148 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA)). Scientific Opinion on the substantiation of a health claim related to DHA and contribution to normal brain development pursuant to Article 14 of Regulation (EC) No 1924/2006. EFSA Journal 2014; 12: 3840
  • 149 Julvez J, Mendez M, Fernandez-Barres S. et al. Maternal Consumption of Seafood in Pregnancy and Child Neuropsychological Development: A Longitudinal Study Based on a Population With High Consumption Levels. Am J Epidemiol 2016; 183: 169-182
  • 150 Hibbeln JR, Davis JM, Steer C. et al. Maternal seafood consumption in pregnancy and neurodevelopmental outcomes in childhood (ALSPAC study): an observational cohort study. Lancet 2007; 369: 578-585
  • 151 Oken E, Radesky JS, Wright RO. et al. Maternal fish intake during pregnancy, blood mercury levels, and child cognition at age 3 years in a US cohort. Am J Epidemiol 2008; 167: 1171-1181
  • 152 Steer CD, Lattka E, Koletzko B. et al. Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age. Am J Clin Nutr 2013; 98: 1575-1582
  • 153 Braarud HC, Markhus MW, Skotheim S. et al. Maternal DHA Status during Pregnancy Has a Positive Impact on Infant Problem Solving: A Norwegian Prospective Observation Study. Nutrients 2018; DOI: 10.3390/nu10050529.
  • 154 Gould JF, Makrides M, Colombo J. et al. Randomized controlled trial of maternal omega-3 long-chain PUFA supplementation during pregnancy and early childhood development of attention, working memory, and inhibitory control. Am J Clin Nutr 2014; 99: 851-859
  • 155 Meldrum S, Dunstan JA, Foster JK. et al. Maternal fish oil supplementation in pregnancy: a 12 year follow-up of a randomised controlled trial. Nutrients 2015; 7: 2061-2067
  • 156 Bischoff-Ferrari HA. Vitamin D: role in pregnancy and early childhood. Ann Nutr Metab 2011; 59: 17-21
  • 157 Dawodu A, Wagner CL. Prevention of vitamin D deficiency in mothers and infants worldwide – a paradigm shift. Paediatr Int Child Health 2012; 32: 3-13
  • 158 Hyppönen E. Preventing vitamin D deficiency in pregnancy: importance for the mother and child. Ann Nutr Metab 2011; 59: 28-31
  • 159 Allerberger F, Wagner M. Listeriosis: a resurgent foodborne infection. Clin Microbiol Infect 2010; 16: 16-23
  • 160 Elsheikha HM. Congenital toxoplasmosis: priorities for further health promotion action. Public Health 2008; 122: 335-353
  • 161 Bundeszentrum für Ernährung. Listeriose und Toxoplasmose. Sicher essen in der Schwangerschaft. Bestell-Nr. 0346. Online: http://www.ble-medienservice.de last access: 31.07.2018
  • 162 Robert Koch-Institut. Infektionsepidemiologisches Jahrbuch meldepflichtiger Krankheiten für 2016. Berlin: Robert Koch-Institut; 2017
  • 163 Schoneberg I. Seltene Infektionskrankheiten in Deutschland. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2008; 51: 539-546
  • 164 Wilking H, Thamm M, Stark K. et al. Prevalence, incidence estimations, and risk factors of Toxoplasma gondii infection in Germany: a representative, cross-sectional, serological study. Sci Rep 2016; 6: 22551
  • 165 EFSA. Scientific Opinion of the Panel on Biological Hazards on a Request of EFSA on Surveillance and monitoring of Toxoplasma in humans, food and animals. EFSA Journal 2007; 583: 1-64
  • 166 Bojar I, Szymanska J. Environmental exposure of pregnant women to infection with Toxoplasma gondii–state of the art. Ann Agric Environ Med 2010; 17: 209-214
  • 167 Lamont RF, Sobel J, Mazaki-Tovi S. et al. Listeriosis in human pregnancy: a systematic review. J Perinat Med 2011; 39: 227-236
  • 168 Oliveira M, Usall J, Solsona C. et al. Effects of packaging type and storage temperature on the growth of foodborne pathogens on shredded ‘Romaine’ lettuce. Food Microbiol 2010; 27: 375-380
  • 169 Sinigaglia M, Bevilacqua A, Campaniello D. et al. Growth of Listeria monocytogenes in fresh-cut coconut as affected by storage conditions and inoculum size. Food Prot 2006; 69: 6
  • 170 Thevenot D, Delignette-Muller ML, Christieans S. et al. Prevalence of Listeria monocytogenes in 13 dried sausage processing plants and their products. Int J Food Microbiol 2005; 102: 85-94
  • 171 Evenson KR, Barakat R, Brown WJ. et al. Guidelines for Physical Activity during Pregnancy: Comparisons From Around the World. Am J Lifestyle Med 2014; 8: 102-121
  • 172 Pfeifer K, Banzer W, Ferrari N. et al. Nationale Empfehlungen für Bewegung und Bewegungsförderung. Köln: Bundeszentrale für gesundheitliche Aufklärung; 2017
  • 173 [Anonym] ACOG Committee Opinion No. 650: Physical Activity and Exercise During Pregnancy and the Postpartum Period. Obstet Gynecol 2015; 126: e135-e142
  • 174 National Institute for Health and Clinical Excellence. Antenatal care for uncomplicated pregnancies. Clinical guideline. Online: https://www.nice.org.uk/guidance/cg62/resources/antenatal-care-for-uncomplicated-pregnancies-pdf-975564597445 last access: 11.07.2107
  • 175 Colberg SR, Sigal RJ, Yardley JE. et al. Physical Activity/Exercise and Diabetes: A Position Statement of the American Diabetes Association. Diabetes Care 2016; 39: 2065-2079
  • 176 Di Mascio D, Magro-Malosso ER, Saccone G. et al. Exercise during pregnancy in normal-weight women and risk of preterm birth: a systematic review and meta-analysis of randomized controlled trials. Am J Obstet Gynecol 2016; 215: 561-571
  • 177 Magro-Malosso ER, Saccone G, Di Mascio D. et al. Exercise during pregnancy and risk of preterm birth in overweight and obese women: a systematic review and meta-analysis of randomized controlled trials. Acta Obstet Gynecol Scand 2017; 96: 263-273
  • 178 da Silva SG, Ricardo LI, Evenson KR. et al. Leisure-Time Physical Activity in Pregnancy and Maternal-Child Health: A Systematic Review and Meta-Analysis of Randomized Controlled Trials and Cohort Studies. Sports Med 2017; 47: 295-317
  • 179 Wiebe HW, Boule NG, Chari R. et al. The effect of supervised prenatal exercise on fetal growth: a meta-analysis. Obstet Gynecol 2015; 125: 1185-1194
  • 180 Aune D, Schlesinger S, Henriksen T. et al. Physical activity and the risk of preterm birth: a systematic review and meta-analysis of epidemiological studies. BJOG 2017; 124: 1816-1826
  • 181 Wen J, Xun P, Chen C. et al. Non-occupational physical activity during pregnancy and the risk of preterm birth: a meta-analysis of observational and interventional studies. Sci Rep 2017; 7: 44842
  • 182 Poyatos-Leon R, Garcia-Hermoso A, Sanabria-Martinez G. et al. Effects of exercise during pregnancy on mode of delivery: a meta-analysis. Acta Obstet Gynecol Scand 2015; 94: 1039-1047
  • 183 Magro-Malosso ER, Saccone G, Di Tommaso M. et al. Exercise during pregnancy and risk of gestational hypertensive disorders: a systematic review and meta-analysis. Acta Obstet Gynecol Scand 2017; 96: 921-931
  • 184 Yu Y, Xie R, Shen C. et al. Effect of exercise during pregnancy to prevent gestational diabetes mellitus: a systematic review and meta-analysis. J Matern Fetal Neonatal Med 2018; 31: 1632-1637
  • 185 Muktabhant B, Lawrie TA, Lumbiganon P. et al. Diet or exercise, or both, for preventing excessive weight gain in pregnancy. Cochrane Database Syst Rev 2015; (06) CD007145 DOI: 10.1002/14651858.CD007145.pub3.
  • 186 Yeo S, Walker JS, Caughey MC. et al. What characteristics of nutrition and physical activity interventions are key to effectively reducing weight gain in obese or overweight pregnant women? A systematic review and meta-analysis. Obes Rev 2017; 18: 385-399
  • 187 Perales M, Artal R, Lucia A. Exercise During Pregnancy. JAMA 2017; 317: 1113-1114
  • 188 Woodley SJ, Boyle R, Cody JD. et al. Pelvic floor muscle training for prevention and treatment of urinary and faecal incontinence in antenatal and postnatal women. Cochrane Database Syst Rev 2017; (12) CD007471
  • 189 Liddle SD, Pennick V. Interventions for preventing and treating low-back and pelvic pain during pregnancy. Cochrane Database Syst Rev 2015; (09) CD001139 DOI: 10.1002/14651858.CD001139.pub4.
  • 190 Shiri R, Coggon D, Falah-Hassani K. Exercise for the Prevention of Low Back Pain: Systematic Review and Meta-Analysis of Controlled Trials. Am J Epidemiol 2018; 187: 1093-1101
  • 191 World Health Organization. Global recommendations on physical activity for health. Genf: World Health Organization; 2010
  • 192 2018 Physical Activity Guidelines Advisory Committee. 2018 Physical Activity Guidelines Advisory Committee Scientific Report. Washington, DC: U.S. Department of Health and Human Services; 2018
  • 193 The American College of Obstetricians and Gynecologists, Committee on Obstetric Practice. Physical Activity and Exercise During Pregnancy and the Postpartum Period. Obstet Gynecol 2015; 126: e135-e142
  • 194 Mottola MF. Physical activity and maternal obesity: cardiovascular adaptations, exercise recommendations, and pregnancy outcomes. Nutr Rev 2013; 71 (Suppl. 01) S31-S36
  • 195 Tudor-Locke C, Craig CL, Brown WJ. et al. How many steps/day are enough? For adults. Int J Behav Nutr Phys Act 2011; 8: 79
  • 196 Baumann H, Bung P, Fallenstein F. et al. Reaction of mother and fetus to physical stress at high altitude. Geburtshilfe Frauenheilkd 1985; 45: 869-876
  • 197 Huch R. Physical activity at altitude in pregnancy. Semin Perinatol 1996; 20: 303-314
  • 198 Bo K, Artal R, Barakat R. et al. Exercise and pregnancy in recreational and elite athletes: 2016 evidence summary from the IOC expert group meeting, Lausanne. Part 1–exercise in women planning pregnancy and those who are pregnant. Br J Sports Med 2016; 50: 571-589
  • 199 Bo K, Artal R, Barakat R. et al. Exercise and pregnancy in recreational and elite athletes: 2016 evidence summary from the IOC expert group meeting, Lausanne. Part 2–the effect of exercise on the fetus, labour and birth. Br J Sports Med 2016; DOI: 10.1136/bjsports-2016-096810.
  • 200 Coll CV, Domingues MR, Goncalves H. et al. Perceived barriers to leisure-time physical activity during pregnancy: A literature review of quantitative and qualitative evidence. J Sci Med Sport 2017; 20: 17-25
  • 201 Brust JC. Ethanol and cognition: indirect effects, neurotoxicity and neuroprotection: a review. Int J Environ Res Public Health 2010; 7: 1540-1557
  • 202 Dolan GP, Stone DH, Briggs AH. A systematic review of continuous performance task research in children prenatally exposed to alcohol. Alcohol Alcohol 2010; 45: 30-38
  • 203 Spohr HL, Steinhausen HC. Fetal alcohol spectrum disorders and their persisting sequelae in adult life. Deutsches Arzteblatt international 2008; 105: 693-698
  • 204 Flak AL, Su S, Bertrand J. et al. The association of mild, moderate, and binge prenatal alcohol exposure and child neuropsychological outcomes: a meta-analysis. Alcohol Clin Exp Res 2014; 38: 214-226
  • 205 European Board and College of Obstetrics & Gynaecology. Position Statement from the European Board and College of Obstetrics & Gynaecology (EBCOG): Alcohol and pregnancy. Online: https://www.ebcog.org/blank-2/2015/11/27/EBCOG-Position-paper-on-Alcohol-and-pregnancy last access: 22.01.2018
  • 206 Shawe J, Delbaere I, Ekstrand M. et al. Preconception care policy, guidelines, recommendations and services across six European countries: Belgium (Flanders), Denmark, Italy, the Netherlands, Sweden and the United Kingdom. Eur J Contracept Reprod Health Care 2015; 20: 77-87
  • 207 Van Heertum K, Rossi B. Alcohol and fertility: how much is too much?. Fertil Res Pract 2017; 3: 10
  • 208 Niclasen J. Drinking or not drinking in pregnancy: the multiplicity of confounding influences. Alcohol Alcohol 2014; 49: 349-355
  • 209 Kesmodel US, Bertrand J, Stovring H. et al. The effect of different alcohol drinking patterns in early to mid pregnancy on the childʼs intelligence, attention, and executive function. BJOG 2012; 119: 1180-1190
  • 210 Leonardi-Bee J, Smyth A, Britton J. et al. Environmental tobacco smoke and fetal health: systematic review and meta-analysis. Arch Dis Child Fetal Neonatal Ed 2008; 93: F351-F361
  • 211 Murin S, Rafii R, Bilello K. Smoking and smoking cessation in pregnancy. Clin Chest Med 2011; 32: 75-91 viii
  • 212 Rebhan B, Kohlhuber M, Schwegler U. et al. Rauchen, Alkohol und Koffeinkonsum von Müttern vor, während und nach der Schwangerschaft – Ergebnisse der Studie „Stillverhalten in Bayern“. Gesundheitswesen 2009; 71: 391-398
  • 213 Reeves S, Bernstein I. Effects of maternal tobacco-smoke exposure on fetal growth and neonatal size. Expert Rev Obstet Gynecol 2008; 3: 719-730
  • 214 Schneider S, Maul H, Freerksen N. et al. Who smokes during pregnancy? An analysis of the German Perinatal Quality Survey 2005. Public Health 2008; 122: 1210-1216
  • 215 Mei-Dan E, Walfisch A, Weisz B. et al. The unborn smoker: association between smoking during pregnancy and adverse perinatal outcomes. J Perinat Med 2015; 43: 553-558
  • 216 Abraham M, Alramadhan S, Iniguez C. et al. A systematic review of maternal smoking during pregnancy and fetal measurements with meta-analysis. PLoS One 2017; 12: e0170946
  • 217 Pereira PP, Da Mata FA, Figueiredo AC. et al. Maternal Active Smoking During Pregnancy and Low Birth Weight in the Americas: A Systematic Review and Meta-analysis. Nicotine Tob Res 2017; 19: 497-505
  • 218 Bundeszentrale für gesundheitliche Aufklärung. Ich bekomme ein Baby. Rauchfrei in der Schwangerschaft. Ratgeber für Schwangere und ihre Partner. Köln: Bundeszentrale für gesundheitliche Aufklärung.
  • 219 Krebsforschungszentrum D. Tabakatlas Deutschland 2015 – Zahlen und Fakten. Online: https://www.dkfz.de/de/tabakkontrolle/download/Publikationen/sonstVeroeffentlichungen/Tabakatlas_auf_einen_Blick-Zahlen_und_Fakten.pdf last access: 29.12.2017
  • 220 Kuntz B, Zeiher J, Starker A. et al. Rauchen in der Schwangerschaft – Querschnittsergebnisse aus KiGGS Welle 2 und Trends. Journal of Health Monitoring 2018; 3: 47-54
  • 221 Bundesinstitut für Risikobewertung. Gesundheitliche Bewertung von Zusatzstoffen für Tabakerzeugnisse und elektronische Zigaretten. Stellungnahme Nr. 045/2015 vom 30. Juli 2015. 2015.
  • 222 CARE Study Group. Maternal caffeine intake during pregnancy and risk of fetal growth restriction: a large prospective observational study. BMJ 2008; 337: a2332
  • 223 Sengpiel V, Elind E, Bacelis J. et al. Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study. BMC Med 2013; 11: 42
  • 224 EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies). Scientific Opinion on the safety of caffeine. EFSA Journal 2015; 13: 4102
  • 225 Lyngso J, Ramlau-Hansen CH, Bay B. et al. Association between coffee or caffeine consumption and fecundity and fertility: a systematic review and dose-response meta-analysis. Clin Epidemiol 2017; 9: 699-719
  • 226 Li J, Zhao H, Song JM. et al. A meta-analysis of risk of pregnancy loss and caffeine and coffee consumption during pregnancy. Int J Gynaecol Obstet 2015; 130: 116-122
  • 227 Jahanfar S, Jaafar SH. Effects of restricted caffeine intake by mother on fetal, neonatal and pregnancy outcomes. Cochrane Database Syst Rev 2015; (06) CD006965 DOI: 10.1002/14651858.CD006965.pub4.
  • 228 [Anonym] Fruchtsaft- und Erfrischungsgetränkeverordnung vom 24. Mai 2004 (BGBl. I S. 1016), die zuletzt durch Artikel 12 der Verordnung vom 5. Juli 2017 (BGBl. I S. 2272) geändert worden ist. Online: https://www.gesetze-im-internet.de/frsaftv_2004/BJNR101600004.html last access 24.07.2018
  • 229 Europäisches Parlament und Rat. Verordnung (EU) Nr. 1169/2011 des europäischen Parlaments und des Rates vom 25. Oktober 2011 betreffend die Information der Verbraucher über Lebensmittel und zur Änderung der Verordnungen (EG) Nr. 1924/2006 und (EG) Nr. 1925/2006 des Europäischen Parlaments und des Rates und zur Aufhebung der Richtlinie 87/250/EWG der Kommission, der Richtlinie 90/496/EWG des Rates, der Richtlinie 1999/10/EG der Kommission, der Richtlinie 2000/13/EG des Europäischen Parlaments und des Rates, der Richtlinien 2002/67/EG und 2008/5/EG der Kommission und der Verordnung (EG) Nr. 608/2004 der Kommission. Amtsbl Europäische Union 2011; L304/18.
  • 230 Bundesinstitut für Risikobewertung. Fragen und Antworten zu Koffein und koffeinhaltigen Lebensmitteln, einschließlich Energy Drinks. Online: https://www.bfr.bund.de/de/fragen_und_antworten_zu_koffein_und_koffeinhaltigen_lebensmitteln__einschliesslich_energy_drinks-194760.html last access: 24.07.2018
  • 231 Renfrew MJ, McCormick FM, Wade A. et al. Support for healthy breastfeeding mothers with healthy term babies. Cochrane Database Syst Rev 2012; (05) CD001141
  • 232 Kohlhuber M, Rebhan B, Schwegler U. et al. Breastfeeding rates and duration in Germany: a Bavarian cohort study. Br J Nutr 2008; 99: 1127-1132
  • 233 Rebhan B, Kohlhuber M, Schwegler U. et al. Infant feeding practices and associated factors through the first 9 months of life in Bavaria, Germany. J Pediatr Gastroenterol Nutr 2009; 49: 467-473
  • 234 Scott JA, Binns CW, Oddy WH. et al. Predictors of breastfeeding duration: evidence from a cohort study. Pediatrics 2006; 117: e646-e655
  • 235 Brown CR, Dodds L, Legge A. et al. Factors influencing the reasons why mothers stop breastfeeding. Can J Public Health 2014; 105: e179-e185
  • 236 Odom EC, Li R, Scanlon KS. et al. Reasons for earlier than desired cessation of breastfeeding. Pediatrics 2013; 131: e726-e732
  • 237 Rasenack R, Schneider C, Jahnz E. et al. Factors Associated with the Duration of Breastfeeding in the Freiburg Birth Collective, Germany (FreiStill). Geburtshilfe Frauenheilkd 2012; 72: 64-69
  • 238 Ayton J, van der Mei I, Wills K. et al. Cumulative risks and cessation of exclusive breast feeding: Australian cross-sectional survey. Arch Dis Child 2015; 100: 863-868
  • 239 Nationale Stillkommission am Bundesinstitut für Risikobewertung. Stillinformationen für Schwangere. Online: https://www.bfr.bund.de/cm/350/stillempfehlungen-fuer-schwangere-deutsch.pdf last access: 31.07.2018
  • 240 Skouteris H, Nagle C, Fowler M. et al. Interventions designed to promote exclusive breastfeeding in high-income countries: a systematic review. Breastfeed Med 2014; 9: 113-127
  • 241 McFadden A, Gavine A, Renfrew MJ. et al. Support for healthy breastfeeding mothers with healthy term babies. Cochrane Database Syst Rev 2017; (02) CD001141
  • 242 Dyson L, McCormick F, Renfrew MJ. Interventions for promoting the initiation of breastfeeding. Cochrane Database Syst Rev 2005; (02) CD001688 DOI: 10.1002/14651858.CD001688.pub2.
  • 243 Lumbiganon P, Martis R, Laopaiboon M. et al. Antenatal breastfeeding education for increasing breastfeeding duration. Cochrane Database Syst Rev 2016; (12) CD006425
  • 244 Balogun OO, OʼSullivan EJ, McFadden A. et al. Interventions for promoting the initiation of breastfeeding. Cochrane Database Syst Rev 2016; (11) CD001688
  • 245 Hannula L, Kaunonen M, Tarkka MT. A systematic review of professional support interventions for breastfeeding. J Clin Nurs 2008; 17: 1132-1143
  • 246 Sinha B, Chowdhury R, Sankar MJ. et al. Interventions to improve breastfeeding outcomes: a systematic review and meta-analysis. Acta Paediatr Suppl 2015; 104: 114-134
  • 247 Schäfer T, Bauer CP, Beyer K. et al. S3-Leitlinie Allergieprävention – Update 2014. Online: http://www.awmf.org/uploads/tx_szleitlinien/061-016l_S3_Allergiepr%25C3%25A4vention_2014-07.pdf last access: 02.08.2016
  • 248 Kramer MS, Kakuma R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Evid Based Child Health 2014; 9: 447-483
  • 249 Kramer MS, Kakuma R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Cochrane Database Syst Rev 2012; (09) CD000133 DOI: 10.1002/14651858.CD000133.pub3.
  • 250 Miles EA, Calder PC. Can Early Omega-3 Fatty Acid Exposure Reduce Risk of Childhood Allergic Disease?. Nutrients 2017; DOI: 10.3390/nu9070784.
  • 251 Gunaratne AW, Makrides M, Collins CT. Maternal prenatal and/or postnatal n-3 long chain polyunsaturated fatty acids (LCPUFA) supplementation for preventing allergies in early childhood. Cochrane Database Syst Rev 2015; (07) CD010085 DOI: 10.1002/14651858.CD010085.pub2.
  • 252 Bisgaard H, Stokholm J, Chawes BL. et al. Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring. N Engl J Med 2016; 375: 2530-2539
  • 253 Hansen S, Strom M, Maslova E. et al. Fish oil supplementation during pregnancy and allergic respiratory disease in the adult offspring. J Allergy Clin Immunol 2017; 139: 104-111.e4
  • 254 Deutsche Gesellschaft für Zahnerhaltung (DGZ), Deutsche Gesellschaft für Zahn-, Mund- und Kieferheilkunde, Deutsche Gesellschaft für Kinderzahnheilkunde (DGKiZ). et al. S2k-Leitlinie: Kariesprophylaxe bei bleibenden Zähnen – grundlegende Empfehlungen. Online: http://www.awmf.org/leitlinien/detail/ll/083-021.html last access: 27.12.2017
  • 255 Public Health Agency of Canada. Preconception Care. In: Public Health Agency of Canada, Family-Centred Maternity and Newborn Care: National Guidelines. Ottawa: Public Health Agency of Canada; 2017
  • 256 American Academy of Pediatric Dentistry (AAPD). Guideline on Perinatal Oral Health Care. Online: http://www.aapd.org/media/policies_guidelines/g_perinataloralhealthcare.pdf last access: 25.07.2018
  • 257 Lopez NJ, Uribe S, Martinez B. Effect of periodontal treatment on preterm birth rate: a systematic review of meta-analyses. Periodontol 2000 2015; 67: 87-130
  • 258 Iheozor-Ejiofor Z, Middleton P, Esposito M. et al. Treating periodontal disease for preventing adverse birth outcomes in pregnant women. Cochrane Database Syst Rev 2017; (06) CD005297
  • 259 da Silva Bastos Vde A, Freitas-Fernandes LB, Fidalgo TK. et al. Mother-to-child transmission of Streptococcus mutans: a systematic review and meta-analysis. J Dent 2015; 43: 181-191
  • 260 Chaffee BW, Gansky SA, Weintraub JA. et al. Maternal oral bacterial levels predict early childhood caries development. J Dent Res 2014; 93: 238-244
  • 261 Kohler B, Andreen I. Mutans streptococci and caries prevalence in children after early maternal caries prevention: a follow-up at 19 years of age. Caries Res 2012; 46: 474-480
  • 262 Meyer K, Khorshidi-Bohm M, Geurtsen W. et al. An early oral health care program starting during pregnancy–a long-term study–phase V. Clin Oral Investig 2014; 18: 863-872
  • 263 Raffauf AB, Kunze M, Ratka-Krüger P. Parodontale Behandlung während der Schwangerschaft. Wissenschaftliche Mitteilung der Deutschen Gesellschaft für Parodontologie (DGParo). Online: http://www.dgzmk.de/uploads/tx_szdgzmkdocuments/WM_PA-Schwangerschaft.pdf last access: 23.04.2018;
  • 264 Schwendicke F, Karimbux N, Allareddy V. et al. Periodontal treatment for preventing adverse pregnancy outcomes: a meta- and trial sequential analysis. PLoS One 2015; 10: e0129060
  • 265 American Dental Association (ADA), ADA Science Institute. Floss/Interdental Cleaners. Online: https://www.ada.org/en/member-center/oral-health-topics/floss last access: 19.05.2018
  • 266 Bundeszahnärztekammer (BZÄK), Deutsche Gesellschaft für Zahn-, Mund- und Kieferheilkunde. Wissenschaftlich abgesicherte Patienteninformation: Professionelle Zahnreinigung (PZR). Online: https://www.bzaek.de/fileadmin/PDFs/pati/bzaekdgzmk/2_03_pzr.pdf last access: 24.04.2017
  • 267 American Dental Association (ADA), ADA Science Institute. Pregnancy. Online : https://www.ada.org/en/member-center/oral-health-topics/pregnancy last access: 19.05.2018
  • 268 Europäisches Parlament und Europäischer Rat. Verordnung (EU) 2017/852 des Europäischen Parlaments und des Rates vom 17. Mai 2017 über Quecksilber und zur Aufhebung der Verordnung (EG) Nr. 1102/2008. Online: http://data.europa.eu/eli/reg/2017/852/oj last access: 19.05.2018
  • 269 Ständige Impfkommission am Robert Koch-Institut (RKI). Empfehlungen der Ständigen Impfkommission (STIKO) am Robert Koch-Institut – 2017/2018. Epidemiologisches Bulletin 2017; 34: 335-371
  • 270 Robert Koch-Institut. Impfen: Häufig gestellte Fragen und Antworten. Kann in der Schwangerschaft und Stillzeit geimpft werden?. Online: https://www.rki.de/SharedDocs/FAQ/Impfen/AllgFr_Allgemeine%20Fragen/FAQ-Liste_AllgFr_Impfen.html%23FAQId3400682 last access: 25.07.2018
  • 271 Ständige Impfkommission (STIKO) am Robert Koch-Institut. Änderung der Empfehlungen zur Impfung gegen Influenza. Epidemiologisches Bulletin 2010; 31: 299-309
  • 272 Shakib JH, Korgenski K, Presson AP. et al. . Pediatrics 2016; DOI: 10.1542/peds.2015-2360.

Zoom Image
Fig. 1 Reference nutrient values – Recommended additional intake in pregnancy according to German Nutrition Society (DGE), expressed as a percentage of the reference value [52].
Zoom Image
Abb. 1 Nährstoffreferenzwerte – empfohlene Zulage nach DGE in der Schwangerschaft in % des Referenzwertes [52].