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DOI: 10.1055/a-1938-0010
Placental and Umbilical Cord Blood Oxidative Stress Level and Telomere Homeostasis in Early Onset Severe Preeclampsia
Funding Information Yozgat Bozok University Scientific Research Foundation – Grant No. 6602b-TF/18-204

Abstract
Objective Although the etiopathogenesis of preeclampsia (PE) is unknown, evidence suggests that it may be associated with increased oxidative stress. Studies have shown that oxidative stress can affect DNA fragments called telomeres. However, the interactions of PE, oxidative stress, and telomere length are not clearly known. This study aims to evaluate the oxidative/anti-oxidative stress balance in the placenta and umbilical cord and examine the effect of oxidative stress on telomeres.
Materials-Method Cord blood and placental samples were collected from 27 pregnant women with severe PE (280/7–336/7 gestational weeks) and 53 healthy pregnant women. Telomere length (TL) was measured by real-time PCR in the cord blood and placenta tissue. Total antioxidant status (TAS) and total oxidant status (TOS) levels were measured in the cord blood and placenta tissue using a colorimetric method.
Results No significant differences were found between groups regarding age, BMI, gravida, parity, and newborn gender (p>0.05). Cord blood and placental TL of PE patients were significantly shorter than the control group, while cord blood and placental TAS and TOS levels were higher (p<0.05). The results of a multivariate logistic regression analysis showed that the level of placental TOS in PE patients (OR=1.212, 95% CI=1.068–1.375) was an independent risk factor affecting PE.
Conclusion This study found that oxidative stress is an independent risk factor in the development of PE and shortens TL in both placental and umbilical cord blood. Future research on telomere homeostasis may offer a new perspective for the treatment of PE.
Publication History
Received: 01 February 2022
Accepted after revision: 18 August 2022
Article published online:
10 October 2022
© 2022. Thieme. All rights reserved.
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References
- 1
Steegers EA,
Von Dadelszen P,
Duvekot JJ.
et al. Pre-eclampsia. Lancet 2010; 376: 631-644
MissingFormLabel
- 2
Zabul P,
Wozniak M,
Slominski AT.
et al. A proposed molecular mechanism of high-dose vitamin d3 supplementation in
prevention and treatment of preeclampsia. Int J Mol Sci 2015; 16: 13043-13064
MissingFormLabel
- 3
Ghosh G,
Grewal J,
Männistö T.
et al. Racial/ethnic differences in pregnancy-related hypertensive disease in
nulliparous women. Ethn Dis 2014; 24: 283
MissingFormLabel
- 4
Aouache R,
Biquard L,
Vaiman D.
et al. Oxidative stress in preeclampsia and placental diseases. Int J Mol Sci 2018;
19: 1496
MissingFormLabel
- 5
Martínez-Ezquerro JD,
Rodriguez-Castañeda A,
Ortiz-Ramirez M.
et al. Oxidative stress, telomere length, and frailty in an old age population. Rev
Invest Clin 2019; 71: 393-401
MissingFormLabel
- 6
Tastekin A,
Ors R,
Demircan B.
et al. Oxidative stress in infants born to preeclamptic mothers. Pediatr Int 2005;
47: 658-662
MissingFormLabel
- 7
Suhail M,
Suhail S,
Gupta BK.
et al. Malondialdehyde and antioxidant enzymes in maternal and cord blood, and their
correlation in normotensive and preeclamptic women. Clin Med Res 2009; 1: 150
MissingFormLabel
- 8
Tenório MB,
Ferreira RC,
Moura FA.
et al. Cross-talk between oxidative stress and inflammation in preeclampsia. Oxid
Med Cell Longev 2019; 2019: 8238727
MissingFormLabel
- 9
Schoots MH,
Bourgonje MF,
Bourgonje AR.
et al. Oxidative stress biomarkers in fetal growth restriction with and without
preeclampsia. Placenta 2021; 115: 87-96
MissingFormLabel
- 10
Correa P,
Palmeiro Y,
Soto M.
et al. Etiopathogenesis, prediction, and prevention of preeclampsia. Hypertens Pregnancy
2016; 35: 280-294
MissingFormLabel
- 11
Blasco MA,
Gasser SM,
Lingner J.
Telomeres and telomerase. Genes Dev 1999; 13: 2353-2359
MissingFormLabel
- 12
Olivieri F,
Lorenzi M,
Antonicelli R.
et al. Leukocyte telomere shortening in elderly type2 DM patients with previous
myocardial infarction. Atherosclerosis 2009; 206: 588-593
MissingFormLabel
- 13
Epel ES,
Blackburn EH,
Lin J.
et al. Accelerated telomere shortening in response to life stress. Proc Natl Acad
Sci 2004; 101: 17312-17315
MissingFormLabel
- 14
Davy P,
Nagata M,
Bullard P.
et al. Fetal growth restriction is associated with accelerated telomere shortening
and
increased expression of cell senescence markers in the placenta. Placenta 2009; 30:
539-542
MissingFormLabel
- 15
Sukenik-Halevy R,
Fejgin M,
Kidron D.
et al. Telomere aggregate formation in placenta specimens of pregnancies complicated
with pre-eclampsia. Cancer Genet Cytogenet 2009; 195: 27-30
MissingFormLabel
- 16
Sukenik-Halevy R,
Amiel A,
Kidron D.
et al.
Telomere homeostasis in trophoblasts and in cord blood cells from pregnancies
complicated with preeclampsia. Am J Obstet Gynecol 2016; 214: 283 e281–283. e287
MissingFormLabel
- 17
Watanabe K,
Naruse K,
Tanaka K.
et al. Outline of definition and classification of “pregnancy induced
hypertension (PIH)”. Hypertens Res Pregnancy 2013; 1: 3-4
MissingFormLabel
- 18
ACOG Committee on Obstetric Practice.
ACOG practice bulletin. Diagnosis and management of preeclampsia and eclampsia.
Number 33, January 2002. American College of Obstetricians and
Gynecologists. Int J Gynaecol Obstet 2002; 77: 67-75
MissingFormLabel
- 19
Minakami H,
Maeda T,
Fujii T.
et al. Guidelines for obstetrical practice in Japan: Japan Society of Obstetrics and
Gynecology (JSOG) and Japan Association of Obstetricians and Gynecologists
(JAOG) 2014 edition. J Obstet Gynaecol Res 2014; 40: 1469-1499
MissingFormLabel
- 20
Yumru M,
Savas HA,
Kalenderoglu A.
et al. Oxidative imbalance in bipolar disorder subtypes: a comparative study. Prog
Neuropsychopharmacol Biol Psychiatry 2009; 33: 1070-1074
MissingFormLabel
- 21
Cawthon RM.
Telomere measurement by quantitative PCR. Nucleic Acids Res 2002; 30: e47-e47
MissingFormLabel
- 22
Ferreira RC,
Fragoso MBT,
Bueno NB.
et al. Oxidative stress markers in preeclamptic placentas: a systematic review with
meta-analysis. Placenta 2020; 99: 89-100
MissingFormLabel
- 23
Kirbas A,
Daglar K,
Gencosmanoglu G.
et al. Total oxidative and anti-oxidative status, and ADAMTS-12 levels in placenta
previa and early-onset severe preeclampsia. Pregnancy Hypertens 2016; 6: 295-299
MissingFormLabel
- 24
Okuda K,
Bardeguez A,
Gardner JP.
et al. Telomere length in the newborn. Pediatric Res 2002; 52: 377-381
MissingFormLabel
- 25
Wojcicki J,
Olveda R,
Heyman M.
et al. Cord blood telomere length in Latino infants: relation with maternal education
and infant sex. J Perinatol 2016; 36: 235-241
MissingFormLabel
- 26
Gielen M,
Hageman G,
Pachen D.
et al. Placental telomere length decreases with gestational age and is influenced
by
parity: a study of third trimester live-born twins. Placenta 2014; 35: 791-796
MissingFormLabel
- 27
Biron-Shental T,
Sukenik-Halevy R,
Sharon Y.
et al. Short telomeres may play a role in placental dysfunction in preeclampsia and
intrauterine growth restriction. Am J Obstet Gynecol 2010; 202: 381.e1-7
MissingFormLabel
- 28
von Zglinicki T,
Saretzki G,
Döcke W.
et al. Mild hyperoxia shortens telomeres and inhibits proliferation of fibroblasts:
a
model for senescence?. Exp Cell Res 1995; 220: 186-193
MissingFormLabel
- 29
Cattan V,
Mercier N,
Gardner JP.
et al. Chronic oxidative stress induces a tissue-specific reduction in telomere length
in CAST/Ei mice. Free Radic Biol Med 2008; 44: 1592-1598
MissingFormLabel
- 30
Houben JM,
Moonen HJ,
van Schooten FJ.
et al. Telomere length assessment: biomarker of chronic oxidative stress?. Free Radic
Biol Med 2008; 44: 235-246
MissingFormLabel
- 31
Xu J,
Ye J,
Wu Y.
et al. Reduced fetal telomere length in gestational diabetes. PloS One 2014; 9: e86161
MissingFormLabel
- 32
Rani N,
Dhingra R,
Arya DS.
et al. Role of oxidative stress markers and antioxidants in the placenta of
preeclamptic patients. J Obstet Gynaecol Res 2010; 36: 1189-1194
MissingFormLabel
- 33
Chiarello DI,
Abad C,
Rojas D.
et al. Oxidative stress: normal pregnancy versus preeclampsia. Biochim Biophys Acta
Mol Basis Dis 2020; 1866: 165354
MissingFormLabel
- 34
Szentpéteri I,
Rab A,
Kornya L.
et al. Placental gene expression patterns of endoglin (CD105) in intrauterine growth
restriction. J Matern Fetal Neonatal Med 2014; 27: 350-354
MissingFormLabel
- 35
Hsu P,
Santner-Nanan B,
Dahlstrom JE.
et al. Altered decidual DC-SIGN+antigen-presenting cells and impaired
regulatory t-cell induction in preeclampsia. Am J Pathol 2012; 181: 2149-2160
MissingFormLabel
- 36
Booth SA,
Wadley GD,
Marques FZ.
et al. Fetal growth restriction shortens cardiac telomere length, but this is
attenuated by exercise in early life. Physiological genomics 2018; 50: 956-963
MissingFormLabel
- 37
Biron-Shental T,
Sukenik-Halevy R,
Sharon Y.
et al. Telomere shortening in intrauterine growth restriction placentas. Early Hum
Dev 2014; 90: 465-469
MissingFormLabel