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DOI: 10.1055/s-0045-1809438
The Impact of Psychological Factors on Periodontitis in the Elderly: A Systematic Review
- Abstract
- Introduction
- Methods
- Results
- Periodontitis and Cognitive Impairment
- Periodontitis and Depression, Stress
- Methodological Quality
- GRADE Tool for Evidence
- Discussion
- Conclusion
- References
Abstract
Psychological factors and periodontitis are prevalent in geriatric populations, with evolving evidence suggesting potential associations. This systematic review comprehensively examines and evaluates the bidirectional relationship between psychological factors and periodontitis in older adults. Following PRISMA guidelines, systematic searches were conducted across PubMed, Google Scholar, Scopus, Embase, and Web of Science databases. The research question was structured using the PECO framework (P = older adults aged ≥ 60 years; E = presence of psychological factors; C = absence of psychological factors; O = periodontitis and its severity). Articles were selected based on predetermined inclusion/exclusion criteria, followed by data extraction. The Newcastle-Ottawa Scale assessed risk of bias and methodological quality, while the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) framework determined evidence certainty. Of 475 studies identified, 13 met the inclusion criteria for qualitative synthesis (8 on depression, 3 on stress, 1 on cognitive impairment, and 1 on examining multiple factors). For depression–periodontitis associations, results were inconsistent: four studies demonstrated positive associations, three found no significant relationship, and one had unclear findings. All three studies investigating stress–periodontitis relationships showed positive associations, suggesting a more consistent connection. The single study on cognitive impairment found significant independent associations with periodontitis after controlling for confounders. Only one longitudinal study (n = 11,454) revealed increased periodontitis risk at both 6-month and 1-year follow-ups in older adults with depression. Based on Newcastle-Ottawa Scale ratings, seven studies were deemed high quality, three moderate quality, and one low quality. GRADE assessment indicated very low certainty of evidence across all psychological factors, primarily due to methodological heterogeneity. This systematic review indicates significant associations between periodontal disease severity and psychological factors, particularly stress and cognitive impairment, in older adults. These findings suggest the importance of integrating psychological assessment into geriatric oral healthcare. More longitudinal research is needed to establish causality and bidirectional relationships, especially in middle- and low-income countries with a rapidly growing geriatric population. Mental health considerations should be incorporated into prevention and treatment strategies for periodontal disease in older adults.
Keywords
periodontitis - psychological factors - older adults - GRADE analysis - oral health - stress - anxiety - depression - cognitive impairment - cardiovascular outcomesIntroduction
With declining fertility rates and rising life expectancies, the global elderly population (60 years and older) has grown substantially from 5% in 1975 to 11.5% in 2019 and is projected to reach 2.1 billion by 2050.[1] [2] Although developed nations currently have a higher percentage of older adults, rapid growth occurs in developing countries.[3] The population of persons aged 80+ years is increasing by 4.0% annually.[3] Reflecting this demographic shift, more older adults are retaining natural teeth. In the United States, edentulism decreased from 38% in 1980 to 4.6% in 2012.[4] Similar patterns are seen in other developed nations like Europe, Japan, and Australia, with declining edentulism rates among older adults.[5] [6] [7] With more retained teeth, periodontitis prevalence may rise in older populations.
Periodontitis is an inflammatory disorder affecting the soft tissue and bone supporting the tooth.[8] It has a complex pathogenesis initiated by subgingival colonization of gram-negative anaerobic bacteria. Interactions between the microbial challenge and host inflammatory response determine disease progression and connective tissue/bone destruction. Periodontitis has a multifactorial etiology with varied clinical presentations. A new classification grades periodontitis (A, B, C) by disease progression risk, treatment response, and potential oral health impact, with grade C being the most rapidly progressive.[9] It stages disease (I, II, III, IV) by severity and complexity, with stage IV being the most severe with altered masticatory function. Stages are designated localized, generalized, or molar-incisor patterns based on affected teeth. Various clinical measurements define periodontal disease cases in research, including probing depth, gingival bleeding, and clinical attachment level. Probing depth in millimeters (mm) from the free gingival margin to the base of the pocket is commonly used.[10] Gingival bleeding indicates active inflammation. Clinical attachment level, measured from the cementoenamel junction to the base of the pocket, is used in epidemiology. Some studies measure alveolar bone loss radiographically to quantify destruction.[8] Differing measures and thresholds to define disease across studies of older adults may hamper prevalence comparison. Partial versus complete mouth assessments also underestimate true prevalence and severity.[11]
Numerous studies have documented periodontitis prevalence and severity in older adults, but progression data are limited, possibly due to the low proportion of adults aged 65+ retaining natural teeth. However, recent NHANES survey data (2018–2019) indicate 63% of older adults have moderate-severe periodontitis, with a small but significant proportion having severe disease.[12] The New England Elders Dental Study of 554 adults aged 70+ similarly found that 66% had moderate periodontitis, with at least one 4- to 5-mm pocket.[7] [13] Other U.S.[14] and global studies[9] [15] [16] report comparable results. Severe 6–7 mm pockets were seen only in one-fifth of older adults. Likewise, only a small percentage have advanced alveolar bone loss.[17] [18] While periodontitis prevalence and severity rise, current consensus disputes age as an independent risk factor. Rather than increased vulnerability, the cumulative effect of prolonged exposure to established periodontal disease risk factors is cited.[19]
Systemic illness is common in older adults. Age-related declines in health, cognition, financial capacity, physical ability, and other functions are expected. Older adults often experience stress due to physical frailty and limited activity. Stressed elderly are more susceptible to periodontitis, as poor oral hygiene, increased glucocorticoid release, suppressed immunity, and insulin resistance are all linked to stress and may increase periodontitis risk.[20] Periodontitis is also associated with other chronic diseases like cardiovascular disease, rheumatoid arthritis, atherosclerosis, and diabetes, reinforcing the role of periodontitis-induced inflammatory mediators entering the bloodstream.[21]
Recent evidence has significantly strengthened our understanding of the relationship between periodontitis and systemic diseases, as comprehensive research by Sanz et al[22] has demonstrated that periodontal inflammation directly contributes to cardiovascular pathology through bacteremia and inflammatory pathways. Their work emphasizes how periodontal pathogens and inflammatory mediators can affect distant organs beyond the oral cavity. Additionally, Ramseier et al[23] have established that effective periodontal treatment can significantly improve cardiovascular disease outcomes, highlighting the clinical importance of maintaining periodontal health in at-risk populations such as the elderly. These findings underscore the need to identify factors influencing periodontal disease progression in geriatric patients.
Given the role of periodontitis in systemic and neuroinflammation,[20] an association between periodontitis and psychological impairment is biologically plausible and clinically relevant. The complex bidirectional relationship between oral health and mental health represents a critical yet understudied aspect of geriatric healthcare. Psychological factors may influence periodontitis development through behavioral mechanisms (affecting oral hygiene practices), neuroendocrine pathways (stress-induced immunomodulation), and inflammatory processes (shared inflammatory mediators). Conversely, periodontitis may exacerbate psychological conditions through chronic inflammation and its effects on neurological function.
Understanding these relationships has significant implications for developing integrated approaches to geriatric healthcare. Clarifying associations between psychological factors and periodontitis could help identify at-risk elderly populations and inform more effective preventive and therapeutic strategies. Thus, this systematic review aims to comprehensively assess and evaluate the relationship between psychological factors and periodontitis in older adults, addressing an important gap in our understanding of geriatric oral health determinants.
Methods
This systematic review followed PRISMA guidelines and the Cochrane Handbook.[24] Before initiation, the protocol was registered on PROSPERO (Reg. no: CRD42023424929).
Focused Question
Is there an association between psychological factors and periodontitis in older adults? The PECOS framework was used: P = older adults aged ≥60 years; E = presence of psychological factors; C = older adults without psychological factors; O = periodontitis severity. This structure ensures consistent alignment between our research question formulation and methodology.
Search Strategy
Two reviewers independently searched PubMed, Cochrane CENTRAL, Embase, Scopus, and other sources like Google Scholar and reference lists, without language restrictions. Ongoing trial registries were searched. Authors were contacted regarding unpublished studies. Manual searches of periodontology and psychology journals were conducted. Reference lists of excluded articles were checked. The detailed search strategy is presented in [Table 1].
Sl. no. |
Domains |
Keywords |
Wildcard |
---|---|---|---|
1 |
Periodontitis |
(Periodontal Loss, Periodontal Attachment) OR (Alveolar Process[a]) OR (Alveolar Resorption[a]) OR (Resorption[a], Alveolar) OR (Bone Loss[a], Periodontal) OR (Periodontal Bone Loss[a]) OR (Periodontal Resorption) OR (Resorption, Periodontal) OR (Alveolar Bone Atroph[a]) OR (Bone Atroph[a], Alveolar) OR (Bone Loss[a], Alveolar) OR (Intra-bony Defects) OR (Bony defect[a]) OR (Defect[a], bony) OR (Bone defect[a]) OR (Defect[a], bone) |
atrophy, atrophies, resorption, resorptions, loss, losses, bone, bony, defect, defects |
2 |
Psychological factors |
(“Depression” OR “depressive disorders” OR “depression symptoms”) OR (“anxiety” OR “mood disorders” OR “psychological distress”) OR (“stress” OR “psychological distress” OR “stress symptom”) OR (“cognitive impairment” OR “cognitive decline” OR “cognitive dysfunction”) |
None |
3 |
Population |
“older adults” OR “elderly” OR “geriatric population” OR “older people” OR “senior citizens” OR “aged 60 and above” OR “vulnerable population” |
None |
4 |
Assessment Tools |
(“Periodontal Probing index” OR “Community Periodontal Index for Treatment Needs” OR “Periodontal Screening and Recording Index”) AND (“HADS” OR “hospital Anxiety and Depression Index” OR “Becks depression Index” OR “BDI” OR “LIPPS Inventory for stress in elderly” OR “DASS” OR “Depression anxiety and stress scale” OR “Mini-Mental State Examination” OR “MMSE” OR “Geriatric Depression Scale” OR “GDS”) |
None |
5 |
Outcome |
(Outcome, Treatment) OR (Patient-Relevant Outcome) OR (Outcome[a], Patient-Relevant) OR (Patient Relevant Outcome) OR (Treatment needs for elderly) OR (Oral health-related quality of life) |
outcome, outcomes |
a Indicates wildcard in PubMed.
For the literature search, we employed comprehensive search terms combining multiple domains: (1) periodontitis and related periodontal conditions; (2) psychological factors including depression, anxiety, stress, and cognitive impairment; (3) geriatric population descriptors; (4) relevant assessment indices; and (5) outcome measurements. The search was structured to capture all relevant publications through October 2024, with no language restrictions applied.
Eligibility Criteria
Original cross-sectional, case–control, longitudinal, and observational studies investigating associations between periodontitis and psychological factors (depression, stress, anxiety, cognitive impairment) in adults aged ≥60 years were included. Studies had to report sample size calculations and use validated tools to assess periodontal health/disease and psychological factors. Self-reported and clinically diagnosed periodontitis were eligible, with a preference for clinical diagnosis. Severe periodontitis was selected over moderate or mild forms. Reviews, letters, in vitro studies, animal studies, case reports, and conference abstracts were excluded. Studies on other oral conditions were not included.
Studies were selected based on clearly defined inclusion criteria regarding population (older adults ≥60 years), exposures (validated measures of psychological factors), comparators (appropriate control or reference groups), outcomes (clinically or radiographically assessed periodontitis), and study design (original research with proper methodology). This approach ensured systematic and reproducible study selection aligned with our research question.
Screening and Selection
Search results were imported into EndNote and Excel. Titles/abstracts were independently screened by two reviewers (R.S.P., A.A.) for relevance. Non-research articles were excluded. Full texts were obtained for potentially relevant articles. Two reviewers (R.S.P., A.A.M.) then assessed full texts for eligibility. Reference lists of included studies were searched. Disagreements were resolved through discussion or a third reviewer (S.A.). The screening process followed a two-stage approach to ensure comprehensive and unbiased selection. Initial screening focused on title and abstract evaluation against predetermined criteria, followed by full-text review of potentially eligible studies. We specifically sought articles examining associations between validated measures of psychological factors and periodontitis in adults ≥60 years. Two reviewers conducted each step independently, with a third reviewer resolving discrepancies.
Data Extraction
Two reviewers (R.S.P., W.I.I.) independently extracted data using a standardized form recording: study design, sample demographics, psychological factor(s) studied, diagnostic/rating tools used, analyses, and key findings. One reviewer (A.A.M.) completed the extraction, and two (R.S.P., S.A.) verified it for accuracy. The data extraction process employed structured forms designed for this review, ensuring comprehensive and consistent information capture across all included studies. Particular attention was given to extracting details about psychological assessment methodologies, periodontal examination protocols, demographic characteristics of participants, and statistical analyses employed, facilitating robust comparison across studies.
Risk of Bias Assessment
The Newcastle-Ottawa Scale assessed the methodological quality of included studies.[25] Using NOS guidelines, each study was assigned a score from 0 to 10 stars. Two reviewers (R.S.P., S.A.) evaluated three domains: sample selection, exposure assessment, and comparability. Scores ≥8 indicated low risk of bias. Scores <4 on ≥2 domains indicated high risk. For cross-sectional studies, we evaluated four selection criteria (representativeness, sample size, nonrespondents, and exposure ascertainment), comparability criteria (control for confounding), and outcome criteria (assessment methods and statistical analysis). For case–control studies, selection criteria included case definition, representativeness, control selection, and control definition; exposure criteria covered exposure ascertainment, assessment methods, and nonresponse rates. This comprehensive approach systematically evaluated internal validity for each included study.
Quantitative Analysis
Due to inconsistencies in participants' age, periodontal assessments, and psychological factor measurements, conducting a meta-analysis was not feasible. Significant heterogeneity was expected. Thus, findings were summarized using the GRADE system.
We thoroughly evaluated the potential for meta-analysis, examining statistical heterogeneity (using I 2 statistics), methodological heterogeneity (differences in study design and quality), and clinical heterogeneity (variations in participant characteristics, interventions, and outcome measurements). Despite identifying several studies with similar psychological constructs and periodontal outcomes, the pronounced methodological differences in assessment tools and reporting formats precluded meaningful statistical pooling. We therefore employed narrative synthesis with GRADE assessment to systematically evaluate evidence quality.
Level of Evidence
The GRADE approach examined the level of evidence. GRADE rates the quality of evidence and strength of recommendations. The level of evidence was rated as low or very low if studies had serious limitations in risk of bias, inconsistency, imprecision, indirectness, or publication bias. GRADE does not assess intervention effects/dosages. Here, it evaluated the evidence for psychological factor–periodontitis associations in older adults. Our GRADE assessment specifically evaluated five domains that might reduce confidence in estimated effects: risk of bias (methodological limitations), inconsistency (unexplained heterogeneity), indirectness (population, intervention, outcome differences from review question), imprecision (wide confidence intervals, small sample sizes), and publication bias (systematic underestimation of effects). Each domain was rated as not serious, serious, or very serious, with the final evidence quality classified as high, moderate, low, or very low. This structured approach provided a transparent evaluation of evidence certainty for each psychological factor–periodontitis relationship.
Results
The database search yielded 475 potential articles, of which 294 were duplicates. After title/abstract screening of the remaining 181 articles, 128 were excluded. The 48 articles receiving full-text review were reduced to 13 included studies after applying eligibility criteria ([Fig. 1]). The remaining were removed for a reason ([Supplementary Tables S1] and [S2] [available in the online version only]). All studies underwent GRADE evidence assessment. The main characteristics of the 13 included studies are presented in [Table 2], categorized by exposure–outcome relationship direction. Four studies examined depression–periodontitis links, three investigated stress–periodontitis associations, two assessed cognitive impairment–periodontitis relationships, and four found no association between psychological factors and periodontitis. Results are presented by psychological factors below.


Authors/Country |
Study design |
Sample size (M/F) |
Age group (years) |
Psychological factors and periodontitis assessment |
Key findings |
---|---|---|---|---|---|
Viana et al[26] Brazil |
Cross-sectional |
191 (35/156) |
60–85 |
Depression: GDS-15 periodontitis: clinical examination |
No association between periodontitis and depression; an association between oral hygiene and depression was observed |
Shin et al[37] South Korea |
Cross-sectional |
189 (98/91) |
60–90 |
Cognitive impairment: MMSE-KC depression: CES-D periodontitis: clinical examination and radiographs |
Periodontitis is independently associated with both cognitive impairment and depression after controlling for confounders |
Botelho et al[34] Portugal |
Cross-sectional |
592 (272/320) |
≥ 65 |
Stress: PSS-10-PT Oral HRQoL: OHIP-14-PT periodontitis: clinical examination |
Self-perceived xerostomia and stress are significantly associated with periodontitis severity |
Persson et al[29] USA |
Cross-sectional |
701 (287/414) |
60–75 |
Depression: GDS periodontitis: clinical examination |
No significant association between depression and periodontitis in elderly participants |
Luca et al[32] Italy |
Case–control |
90 (31/59) |
≥ 60 |
Depression: DSM-IV criteria, periodontitis: clinical examination |
Significant correlation between psychiatric variables and poor periodontal health status |
Skośkiewicz-Malinowska et al[30] Poland |
Cross-sectional |
500 (180/320) |
65–99 |
Depression: PHQ-9 periodontitis: clinical examination |
No association between periodontitis and depression; an association between oral hygiene and depression was detected |
Coelho et al[36] Brazil |
Cross-sectional |
621 (321/300) |
60–85 |
Stress: Perceived Stress Scale periodontitis: clinical attachment loss |
A significant association between stress and periodontitis is attributed to the multifactorial nature of both conditions |
Hugo et al[38] Brazil |
Cross-sectional |
230 (not specified) |
60–75 |
Stress: ISSL depression: BDI periodontitis: GBI and probing depth |
A complex relationship between stress and periodontitis was identified; no association between depression and periodontitis |
Hilgert et al[35] Brazil |
Cross-sectional |
235 (not specified) |
60–84 |
Stress: ISSL periodontitis: clinical examination cortisol: salivary assay |
No association found between cortisol levels, stress measures, and periodontitis parameters |
Youn et al[31] Korea |
Cross-sectional |
2002 (872/1134) |
≥ 65 |
Depression: ISSL sleep: questionnaire periodontitis: clinical examination |
A significant association was found between depression, sleep disturbance, and periodontitis severity |
Kim et al[28] Korea |
Longitudinal |
11,454 (not specified) |
≥ 66 |
Depression: ISSL periodontitis: clinical diagnosis (database) |
Significant association between depression and chronic periodontitis at 6-mo and 1-y follow-ups |
Iwasaki et al[27] Japan |
Cross-sectional |
85 (not specified) |
≥ 75 |
Depression: not specified, cognitive decline: assessment, periodontitis: CAL ≥6 mm |
A significant association was found between cognitive decline and severe periodontitis |
Kjellström et al[33] Sweden |
Case–control |
1,610 (not specified) |
65–85 |
Depression: assessment periodontitis: panoramic radiography |
No significant difference in depression symptoms between those with and without periodontitis |
Abbreviations: OHIP-14-PT, Oral Health Impact Profile-14 Portuguese version; PSS-10-PT, Perceived Stress Scale-10 Portuguese version; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders, 4th edition; PHQ-9, Patient Health Questionnaire-9; ISSL, Lipp's Inventory of Stress Symptoms for Adults; BDI, Beck's Depression Index; GBI, Gingival Bleeding Index; CAL, Clinical Attachment Loss; HRQoL, health-related quality of life.
Depression–Periodontitis
Eight studies examined depression–periodontitis associations, considering depression as the exposure and periodontitis as the outcome. Studies were conducted between 2003 and 2022 with sample sizes ranging from 191 to 11,545. One study was from Brazil[26]; the rest were from high-income countries. There were four cross-sectional,[27] [28] [29] [30] [31] [32] [33] three case–control,[27] [32] [33] and one longitudinal study.[28] Various depression scales were used. Periodontitis was assessed by clinical examination (six studies) or radiographs (two studies). In the longitudinal study by Kim et al[28] in 11,545 older South Koreans, depressive mood was associated with periodontitis at 6-month and 1-year follow-ups. All studies were controlled for confounders like age, sex, and smoking. Meta-analysis was precluded by heterogeneity across studies. Of the eight studies examining depression–periodontitis relationships, four demonstrated positive associations, while three found no significant relationship, and one showed unclear associations. This inconsistency in findings may reflect methodological differences in depression assessment tools, with studies employing various instruments including the Geriatric Depression Scale (GDS), Beck's Depression Inventory (BDI), and Patient Health Questionnaire (PHQ-9). Additionally, different approaches to periodontitis assessment (clinical vs. radiographic) may have contributed to the variability in results.
Periodontitis and Stress
Three cross-sectional studies examined the association between stress (exposure) and periodontitis (outcome). Sample sizes ranged from 235 to 621. One study was conducted in Portugal[34] and two in Brazil.[35] [36] Different validated stress scales were used, including the Perceived Stress Scale (two studies) and Lipp's Inventory of Stress Symptoms for Adults (one study). Periodontitis was assessed via clinical examination for pocket depth ≥4 mm (one study), clinical attachment loss >4 mm (one study), Community Periodontal Index (one study), and radiographic bone loss >0 mm (one study). Two studies had a moderate risk of bias[34] [36] and one had a low risk.[35] Confounding was controlled statistically. The small number and heterogeneity between studies precluded meta-analysis. All three studies examining stress–periodontitis relationships demonstrated positive associations, suggesting a more consistent relationship than observed with depression. This consistency is particularly noteworthy given the methodological variations across studies. The findings align with established biological mechanisms linking stress to periodontal health through immune function alterations, behavioral changes affecting oral hygiene, and potential direct effects on periodontal tissues.
Periodontitis and Cognitive Impairment
One study examined associations between periodontitis, cognitive impairment, and depression.[37] This cross-sectional study was conducted in South Korea in 2016 with 189 older adults. Periodontitis was assessed by clinical examination of pocket depth and clinical attachment loss using digital panoramic radiographs. Cognitive impairment was measured with the Mini-Mental State Examination Korean version (MMSE-KC) and depression with Beck's depressive scale. This study was rated as having good methodological quality. Statistical analysis revealed that cognitive impairment and depression were independently associated with chronic periodontitis, after controlling for confounders like age, sex, occupation, and smoking ([Table 2]).
It is important to note that our systematic search identified numerous studies investigating the relationship between periodontitis and cognitive impairment. Still, many did not meet our strict inclusion criteria regarding age group (≥60 years exclusively), assessment tools, or reporting methods. The literature in this field has expanded substantially in recent years, with a notable meta-analysis by Guo et al[53] incorporating 20 studies on this topic. Their analysis demonstrated significant associations between periodontal disease and cognitive impairment across diverse populations. The neuroinflammatory pathway linking periodontitis and cognitive decline has received increasing research attention. Periodontal pathogens and their byproducts may contribute to neuroinflammation through systemic circulation, potentially exacerbating neurodegenerative processes. This mechanism aligns with findings from Wu et al[54] and Dziedzic A[55], who identified significant relationships between periodontal parameters and cognitive function in older adults. While our review identified only one study meeting all inclusion criteria, the broader literature strongly suggests this remains an important area for further investigation, with a specific focus on geriatric populations.
Periodontitis and Depression, Stress
One cross-sectional study[38] conducted in Brazil, with 230 older adults evaluated, examined the associations between chronic periodontitis (outcome) and stress and depression (exposures). Periodontitis was assessed using the gingival bleeding index and probing depth. Stress was measured with the Lipp's Inventory of Stress Symptoms for Adults (ISSL) and depression with Beck's Depression Index (BDI). Results showed a complex relationship between stress and periodontitis, but no association between depression and periodontitis. This study by Hugo et al.[38] provides valuable insights into the complex interplay between multiple psychological factors and periodontitis. Their findings suggest that the relationship between stress and periodontitis may involve various pathways, not limited to immune system changes alone. The differential findings for stress versus depression highlight the importance of examining specific psychological constructs rather than general “psychological factors” when investigating relationships with periodontal health.
Methodological Quality
Methodological quality was assessed using the Newcastle-Ottawa Scale (NOS) for cross-sectional and case–control studies ([Tables 3] and [4]). Based on NOS ratings, seven studies were deemed high quality, three moderate quality, and one low quality with high risk of bias. The main limitations in lower-quality studies were a lack of case verification, inadequate validation of exposures, and omission of nonresponse rates.[33] Moderate issues with case selection, sample size, and response rates existed in three studies.[29] [34] [36] Most studies[26] [27] [28] [31] [32] [35] [38] had a low risk of bias for exposure–outcome assessment using valid instruments. Questionnaire-based studies appeared more susceptible to bias. Despite similar settings and cohorts, meta-analysis was precluded by differences in periodontitis, psychological factors, outcome measurements, and varying methodological quality. This would introduce substantial heterogeneity and inconsistency. Thus, findings are summarized using the GRADE approach.
Assessment domain |
Evaluation criteria |
Viana et al[26] |
Shin et al[37] |
Botelho et al[34] |
Persson et al[29] |
Youn et al[31] |
Coelho et al[36] |
Hugo et al[38] |
Hilgert et al[35] |
---|---|---|---|---|---|---|---|---|---|
Selection |
Representativeness of sample |
* |
** |
** |
** |
* |
** |
** |
** |
Sample size |
** |
* |
* |
** |
** |
* |
* |
* |
|
Nonrespondent |
* |
* |
* |
– |
– |
* |
* |
* |
|
Uncertainty of exposure |
– |
– |
– |
– |
* |
– |
– |
– |
|
Comparability |
Control for confounding |
N/A |
* |
N/A |
N/A |
* |
N/A |
N/A |
N/A |
Outcome |
Assessment of outcome |
* |
* |
* |
* |
* |
* |
* |
* |
Statistical tests |
** |
** |
* |
* |
* |
* |
* |
* |
|
Overall quality rating |
Good |
Good |
Moderate |
Moderate |
Good |
Moderate |
Good |
Good |
Notes:
• Rating system: * = one star, ** = two stars, - = zero stars, N/A = not applicable.
• Overall quality rating: good = 7–10 stars; moderate = 5–6 stars.
• The Newcastle-Ottawa Scale evaluates methodological quality across three domains: selection of study groups, comparability of groups, and assessment of outcomes.
Assessment domain |
Evaluation criteria |
Luca et al[32] |
Iwasaki et al[27] |
Kjellström et al[33] |
---|---|---|---|---|
Selection |
Case definition adequate |
* |
* |
** |
Representativeness of cases |
** |
** |
* |
|
Selection of controls |
* |
* |
– |
|
Definition of controls |
* |
– |
||
Comparability |
Control for confounding |
** |
N/A |
N/A |
Exposure |
Ascertainment of exposure |
– |
* |
– |
Same method of ascertainment for case and control |
* |
* |
* |
|
Nonresponse rate |
– |
– |
– |
|
Overall quality rating |
Good |
Good |
Poor |
Notes:
• Rating system: * = one star, ** = two stars, - = zero stars, N/A = not applicable.
• Overall quality rating: good = 7–10 stars; poor = 0–4 stars.
• The Newcastle-Ottawa Scale evaluates methodological quality across three domains: selection of study groups, comparability of groups, and assessment of exposure.
GRADE Tool for Evidence
The GRADE approach evaluated the level of evidence for associations between periodontitis and depression, stress, and cognitive impairment in older adults. Overall, the evidence was rated as low or very low quality in most studies. Several limitations may have impacted study outcomes, including flaws in methodology, design, sample size, and validation of measures.[39] [40] Heterogeneity in these factors likely contributed to inconsistent results across studies ([Table 5]). Our GRADE assessment revealed that the evidence quality was constrained primarily by methodological limitations, inconsistency across studies, and indirectness in addressing the primary research question. For depression–periodontitis associations, the evidence was particularly heterogeneous, with some studies showing positive associations and others finding no relationship. The proof of stress–periodontitis associations was more consistent but still limited by methodological concerns. The limited number of studies meeting inclusion criteria for cognitive impairment restricted our ability to establish high-quality evidence, despite promising findings from the included research and broader literature. The overall low to very low GRADE ratings do not necessarily indicate an absence of relationships between psychological factors and periodontitis, but rather highlight the need for more methodologically rigorous studies specifically focused on older adult populations. Future research should employ standardized assessment tools, clearly defined periodontal parameters, and longitudinal designs to strengthen the evidence base in this important area.
No. of studies |
Study design |
Risk of bias |
Inconsistency |
Indirectness |
Imprecision |
Publication bias |
Impact |
Certainty |
---|---|---|---|---|---|---|---|---|
Periodontitis and depression ( n = 8) |
Cross-sectional[a] (n = 4) Case–control[a] (n = 3) Longitudinal[a] (n = 1) |
Very serious[b] |
Very serious[c] |
Very serious[c] |
Not serious |
Highly suspected[d] |
Of the 8 depression-periodontitis studies, 4 found a positive association, 3 found no association, and 1 was inconclusive |
⨁◯◯◯ Very low |
Periodontitis and stress ( n = 3) |
Cross-sectional (n = 3) |
Very serious[b] |
Very serious[c] |
Very serious[c] |
Not serious |
Highly suspected[d] |
All 3 studies found a positive association between stress and periodontitis in the elderly |
⨁◯◯◯ Very low |
Periodontitis and cognitive impairment ( n = 1) |
Cross-sectional[a] (n = 1) |
Very serious[b] |
Very serious[c] |
Very serious[c] |
Not serious |
Highly suspected[d] |
Cognitive impairment and depression were independently associated with periodontitis |
⨁◯◯◯ Very low |
Abbreviation: CI, confidence interval.
a Observational studies are at higher risk of bias due to the criteria of exposed and unexposed population.
b Heterogeneity of instruments to measure periodontitis and depression, stress, and cognitive impairment.
c The majority of evidence is from the geriatric population of either home care, small sample from selected population not from geriatric population in general.
d Most of the observational studies are prone to publication bias as they do not have registration procedures like randomized control and clinical trials.
Discussion
This systematic review used GRADE analysis to examine associations between psychological factors and periodontitis progression in older adults. Our findings revealed important patterns across the included studies: positive associations were found when stress and cognitive impairment were investigated as exposures for periodontitis in five included studies. The stress–periodontitis relationship demonstrated consistent results across all three studies examining this factor. However, results were inconsistent across the nine studies exploring depression–periodontitis links, with most showing no clear association. This aligns with a prior systematic review by Cademartori et al,[41] finding no depression–periodontitis association, despite their meta-analysis indicating an independent relationship. The relationship between periodontitis and systemic conditions has recently gained significant attention. Notably, Sanz et al[22] demonstrated that periodontal inflammation contributes to cardiovascular diseases through direct bacteremia and indirect inflammatory mediator pathways. Their comprehensive review established periodontitis as an important risk factor for cardiovascular outcomes that warrants clinical attention. Additionally, Ramseier et al[23] established that periodontal treatment improves cardiovascular disease outcomes, highlighting the clinical significance of maintaining periodontal health in older adults. These findings underscore the importance of understanding how psychological factors might influence periodontal health, potentially mediating broader systemic health consequences.
The underlying mechanisms remain unclear, while included studies consistently demonstrate links between psychological factors and poor oral health behaviors. Both behavioral and biological pathways have been proposed.[34] [42] [43] Over the past decade, strong associations have emerged between stress/depression and unhealthy behaviors like smoking, excessive alcohol use, poor diet, and sedentary lifestyles.[11] [17] [19] [20] [44] By worsening oral health-related quality of life, depression and stress may also negatively impact self-perceived oral health. Biologically, these factors have been associated with reduced salivary flow, increased oral inflammation, and immune system dysfunction,[6] [45] [46] which may precipitate periodontitis. Further research is needed to elucidate the behavioral and biological mechanisms linking psychological factors to increased periodontitis susceptibility in older populations.
Regarding depression–periodontitis, eight studies were included, with four suggesting a positive association, three no association, and one an unclear relationship. Our mixed results align with prior reviews. Positive findings support hypotheses that depressed patients have heightened proinflammatory cytokines and acute phase proteins, thereby increasing the risk of periodontal disease.[47] [48] Poor oral health from periodontitis may also increase depression risk via embarrassment, social isolation, etc.[10] [49] However, Arias-Bujanda et al[48] noted that despite low risk of bias, high heterogeneity in depression and periodontitis assessments may obscure relationships.
In the depression–periodontitis studies, inconsistencies in the instruments used to assess depression (three different validated tools) likely contributed to the unclear associations found. Additionally, while all participants were older adults, differences in periodontitis assessment via clinical exam versus radiographs may explain the discordant results. This methodological heterogeneity highlights the need for standardized approaches in future research to enable more robust comparisons across studies. The use of different depression screening tools with varying sensitivity and specificity in geriatric populations could significantly impact findings, as noted in previous studies examining oral health–mental health relationships. Another systematic review also found no clear depression–periodontitis association, citing differences in methodological quality.[50] The inclusion of longitudinal, case–control, and cross-sectional studies with representative samples provides relative strength in the current review.
For stress, depression, and periodontitis, included studies generally found positive associations between exposures and outcomes. However, one study showed a complex stress–periodontitis relationship but no link to depression,[38] unlike a prior review indicating negative stress–periodontitis associations.[51] Methodological factors may again account for these discrepancies. Overall, the included studies were of high methodological quality, supporting a potential positive association between psychological factors and periodontitis in older adults that warrants further investigation.
The single study meeting our inclusion criteria that examined cognitive impairment–periodontitis associations found positive relationships.[37] Proposed mechanisms involve oral bacteria entering the bloodstream, breaching the blood–brain barrier, and contributing to neuroinflammation and cognitive decline.[52] This promising area of research has expanded considerably in recent years, with multiple studies and reviews exploring this relationship. The systematic review and meta-analysis by Guo et al[53] analyzed 20 studies and found significant associations between periodontal disease parameters and the risk of cognitive impairment. Additional research by Usuga-Vacca et al[56] has further substantiated these relationships, proposing common inflammatory pathways. While our strict inclusion criteria resulted in only one study being included, the broader literature strongly suggests this remains an important area for geriatric oral health research.
Several limitations in the included studies should be acknowledged when interpreting our findings. Methodological issues in periodontitis assessment in older adults were noted across multiple studies.[33] [37] Periodontitis was assessed using varying methods (clinical examination, radiographs) and parameters (pocket depth, clinical attachment loss, bone loss), making direct comparisons challenging. Additionally, most studies used panoramic radiographs for bone loss assessment, which may not capture the full extent of periodontal destruction. Different psychological assessment tools further complicate interpretation, as these instruments vary in their psychometric properties and clinical thresholds, particularly for geriatric populations with potential comorbidities.
Limitations of this review include the limited literature available focusing specifically on older adults and the few psychological outcomes examined. The predominance of cross-sectional data limits causal inference about periodontitis and psychological factor relationships. Confounding factors were also poorly described. However, strengths include the GRADE evaluation demonstrating the methodological quality, including mostly high-quality studies with representative samples and adjusted analyses, and considering exposure–outcome directionality. Our review also employed a comprehensive search strategy across multiple databases, strict inclusion criteria focusing specifically on geriatric populations, and systematic assessment of evidence quality using established tools like NOS and GRADE, enhancing the reliability of our findings despite the limited available literature. This systematic review provides insights into potential associations between psychological factors and periodontitis in older adults that warrant further investigation using rigorous longitudinal designs. Future research should prioritize longitudinal studies examining bidirectional relationships between psychological factors and periodontitis; standardized assessment protocols for both periodontal parameters and psychological constructs; and consideration of potential mediating factors such as oral hygiene behaviors, systemic inflammation, and healthcare utilization patterns. Additionally, intervention studies evaluating whether addressing psychological factors improves periodontal outcomes would provide valuable clinical guidance for integrated approaches to geriatric oral healthcare.
Conclusion
This systematic review and GRADE analysis indicate significant associations between psychological factors and periodontitis in older adults. Our findings demonstrate remarkably consistent relationships between stress and periodontitis, while the evidence for depression–periodontitis links showed more variable results. Cognitive impairment, though represented by fewer studies meeting our inclusion criteria, showed promising associations with periodontal disease that align with the broader literature on neuroinflammation and oral health. Although most included studies were cross-sectional, the single longitudinal study revealed increased risks of periodontitis in individuals with depression at both 6-month and 1-year follow-ups, suggesting temporal relationships that warrant further investigation. These findings have important clinical implications, suggesting that psychological assessment should be integrated into periodontal care protocols for elderly patients.
More longitudinal research is needed to examine bidirectional relationships and determine causality between periodontitis and psychological factors. Additionally, intervention studies exploring whether addressing psychological factors improves periodontal outcomes would provide valuable clinical guidance. Future research should employ standardized assessment methodologies for periodontal and psychological parameters to strengthen the evidence base and facilitate more robust cross-study comparisons. Additionally, further studies focused on oral health needs of older populations are recommended, particularly in middle- and low-income countries where geriatric growth is rapid. This review provides insights into links between psychological factors and periodontitis in the elderly, which may help clinicians and policymakers consider psychological well-being when addressing oral health issues in this demographic. In conclusion, findings indicate mental health factors should be considered in prevention and treatment strategies for periodontal disease in older adults.
Conflict of Interest
None declared.
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Authors' Contributions
R.S.P.: Concept and design, data collection, data analysis, drafting the manuscript, critical review, and editing; S.A.: Concept and design, data analysis, drafting the manuscript, critical review, and project supervision; W.I.I.: Data collection, manuscript review, and editing; A.A.M.: Data collection, manuscript review, and editing; T.D.: Data collection, manuscript editing; M.N.A.: Data collection, manuscript editing.
All authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part are appropriately investigated and resolved. All authors have read and agreed to the published version of the manuscript.
-
References
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- 2 WHO. Trends in maternal mortality 2000 to 2017: estimates by WHO, UNICEF, UNFPA, World Bank Group and the United Nations Population Division: World Health Organization; 2019
- 3 Bongaarts J. Human population growth and the demographic transition. Philos Trans R Soc Lond B Biol Sci 2009; 364 (1532): 2985-2990
- 4 Slade GD, Akinkugbe AA, Sanders AE. Projections of U.S. Edentulism prevalence following 5 decades of decline. J Dent Res 2014; 93 (10) 959-965
- 5 Sepolia S, Verma P. Periodontal oral health in geriatric patients: an observational study. Journal of Advanced Medical and Dental Sciences Research 2020; 8 (11) 223-228
- 6 Solis AC, Lotufo RF, Pannuti CM, Brunheiro EC, Marques AH, Lotufo-Neto F. Association of periodontal disease to anxiety and depression symptoms, and psychosocial stress factors. J Clin Periodontol 2004; 31 (08) 633-638
- 7 Douglass CW, Jette AM, Fox CH. et al. Oral health status of the elderly in New England. J Gerontol 1993; 48 (02) M39-M46
- 8 Armitage GC. Periodontal diagnoses and classification of periodontal diseases. Periodontol 2000 2004; 34 (01) 9-21
- 9 Jin LJ, Armitage GC, Klinge B, Lang NP, Tonetti M, Williams RC. Global oral health inequalities: task group–periodontal disease. Adv Dent Res 2011; 23 (02) 221-226
- 10 Guentsch A, Pfister W, Cachovan G. et al. Oral prophylaxis and its effects on halitosis-associated and inflammatory parameters in patients with chronic periodontitis. Int J Dent Hyg 2014; 12 (03) 199-207
- 11 Kingman A, Albandar JM. Methodological aspects of epidemiological studies of periodontal diseases. Periodontol 2000 2002; 29 (01) 11-30
- 12 Eke PI, Dye BA, Wei L, Thornton-Evans GO, Genco RJ. CDC Periodontal Disease Surveillance workgroup: James Beck (University of North Carolina, Chapel Hill, USA), Gordon Douglass (Past President, American Academy of Periodontology), Roy Page (University of Washington). Prevalence of periodontitis in adults in the United States: 2009 and 2010. J Dent Res 2012; 91 (10) 914-920
- 13 Fox CH, Jette AM, McGuire SM, Feldman HA, Douglass CW. Periodontal disease among New England elders. J Periodontol 1994; 65 (07) 676-684
- 14 Phillips LL, Paukert AL, Stanley MA, Kunik ME. Incorporating religion and spirituality to improve care for anxiety and depression in older adults. Geriatrics 2009; 64 (08) 15-18
- 15 Montero-Aguilar M, Muñoz-Torres F, Elías-Boneta AR, Dye B, Joshipura KJ. High levels of periodontal disease among the older adult population in San Juan, Puerto Rico. Community Dent Health 2012; 29 (03) 224-228
- 16 Nankwanga A, Phillips J, Neema S. Exploring and curbing the effects of HIV/AIDS on elderly people in Uganda. JCHS 2009 4. 02
- 17 Cho SM, Saw YM, Saw TN. et al. Prevalence and risk factors of anxiety and depression among the community-dwelling elderly in Nay Pyi Taw Union Territory, Myanmar. Sci Rep 2021; 11 (01) 9763
- 18 Farsi N, Al Amoudi N, Farsi J, Bokhary S, Sonbul H. Periodontal health and its relationship with salivary factors among different age groups in a Saudi population. Oral Health Prev Dent 2008; 6 (02) 147-154
- 19 Burt BA. Periodontitis and aging: reviewing recent evidence. J Am Dent Assoc 1994; 125 (03) 273-279
- 20 Friedlander AH, Norman DC. Late-life depression: psychopathology, medical interventions, and dental implications. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002; 94 (04) 404-412
- 21 Al-Zahrani MS, Borawski EA, Bissada NF. Periodontitis and three health-enhancing behaviors: maintaining normal weight, engaging in recommended level of exercise, and consuming a high-quality diet. J Periodontol 2005; 76 (08) 1362-1366
- 22 Sanz M, Marco Del Castillo A, Jepsen S. et al. Periodontitis and cardiovascular diseases: consensus report. J Clin Periodontol 2020; 47 (03) 268-288
- 23 Ramseier CA, Klima S, Klima E, Enkling N. Dental anxiety in Switzerland: trends in prevalence and associations with socioeconomic factors in 2010 and 2017. Swiss Dent J 2023; 134 (01) 52-71
- 24 Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009; 151 (04) 264-269 , W64
- 25 Margulis AV, Pladevall M, Riera-Guardia N. et al. Quality assessment of observational studies in a drug-safety systematic review, comparison of two tools: the Newcastle-Ottawa Scale and the RTI item bank. Clin Epidemiol 2014; 6: 359-368
- 26 Viana LRF, Castro CP, Pereira H-BW, Pereira AdFV, Lopes FF. Is depression associated with periodontal status in elderly?. Braz J Oral Sci 2013; 12: 20-22
- 27 Iwasaki M, Yoshihara A, Kimura Y. et al. Longitudinal relationship of severe periodontitis with cognitive decline in older Japanese. J Periodontal Res 2016; 51 (05) 681-688
- 28 Kim YR, Son M, Nam SH. Association between depressive mood and chronic periodontitis among senior residents using the National Health Insurance Service-Senior Cohort Database. J Periodontol 2023; 94 (06) 742-750
- 29 Persson GR, Persson RE, MacEntee CI, Wyatt CC, Hollender LG, Kiyak HA. Periodontitis and perceived risk for periodontitis in elders with evidence of depression. J Clin Periodontol 2003; 30 (08) 691-696
- 30 Skośkiewicz-Malinowska K, Malicka B, Ziętek M, Kaczmarek U. Oral health condition and occurrence of depression in the elderly. Medicine (Baltimore) 2018; 97 (41) e12490
- 31 Youn H-Y, Shin H-E, Cho M-J. Association of sleep duration and depression with periodontitis in older people aged 65 years and older. J Dental Hygiene Science 2019; 19 (03) 205-212
- 32 Luca M, Luca A, Grasso CMAV, Calandra C. Nothing to smile about. Neuropsychiatr Dis Treat 2014; 10: 1999-2008
- 33 Kjellström B, Gustafsson A, Nordendal E. et al; PAROKRANK Steering Committee. Symptoms of depression and their relation to myocardial infarction and periodontitis. Eur J Cardiovasc Nurs 2017; 16 (06) 468-474
- 34 Botelho J, Machado V, Proença L. et al. Perceived xerostomia, stress and periodontal status impact on elderly oral health-related quality of life: findings from a cross-sectional survey. BMC Oral Health 2020; 20 (01) 199
- 35 Hilgert JB, Hugo FN, Bandeira DR, Bozzetti MC. Stress, cortisol, and periodontitis in a population aged 50 years and over. J Dent Res 2006; 85 (04) 324-328
- 36 Coelho JMF, Miranda SS, da Cruz SS. et al. Is there association between stress and periodontitis?. Clin Oral Investig 2020; 24 (07) 2285-2294
- 37 Shin HS, Shin MS, Ahn YB, Choi BY, Nam JH, Kim HD. Periodontitis is associated with cognitive impairment in elderly Koreans: results from the Yangpyeong Cohort Study. J Am Geriatr Soc 2016; 64 (01) 162-167
- 38 Hugo FN, Hilgert JB, Bozzetti MC. et al. Chronic stress, depression, and cortisol levels as risk indicators of elevated plaque and gingivitis levels in individuals aged 50 years and older. J Periodontol 2006; 77 (06) 1008-1014
- 39 Sutherland SE. Evidence-based dentistry: Part IV. Research design and levels of evidence. J Can Dent Assoc 2001; 67 (07) 375-378
- 40 Cadden SW. Orofacial pain. Guidelines for assessment, diagnosis, and management, 4th edition (2008). Eur J Orthod 2009; 31 (02) 216-217
- 41 Cademartori MG, Gastal MT, Nascimento GG, Demarco FF, Corrêa MB. Is depression associated with oral health outcomes in adults and elders? A systematic review and meta-analysis. Clin Oral Investig 2018; 22 (08) 2685-2702
- 42 Allan CE, Valkanova V, Ebmeier KP. Depression in older people is underdiagnosed. Practitioner 2014; 258 (1771): 19-22 , 2–3
- 43 Bentley SM, Pagalilauan GL, Simpson SA. Major depression. Med Clin North Am 2014; 98 (05) 981-1005
- 44 Haas AN, Gaio EJ, Oppermann RV, Rösing CK, Albandar JM, Susin C. Pattern and rate of progression of periodontal attachment loss in an urban population of South Brazil: a 5-years population-based prospective study. J Clin Periodontol 2012; 39 (01) 1-9
- 45 Subramanian AK, Narayan V, Navaneethan R. Oxidative Stress and Oral Diseases. In: Maurya PK, Dua K. eds. Role of Oxidative Stress in Pathophysiology of Diseases. Singapore: Springer; 2020: 1-12
- 46 Tong D, Dawson J, Love R. Factors affecting oral health status in an elderly military veteran population in New Zealand. J Mil Veterans Health 2010; 18 (03) 12-17
- 47 Dumitrescu AL. Depression and inflammatory periodontal disease considerations - an interdisciplinary approach. Front Psychol 2016; 7: 347
- 48 Arias-Bujanda N, Regueira-Iglesias A, Balsa-Castro C, Nibali L, Donos N, Tomás I. Accuracy of single molecular biomarkers in saliva for the diagnosis of periodontitis: a systematic review and meta-analysis. J Clin Periodontol 2020; 47 (01) 2-18
- 49 Belvederi Murri M, Pariante C, Mondelli V. et al. HPA axis and aging in depression: systematic review and meta-analysis. Psychoneuroendocrinology 2014; 41: 46-62
- 50 Zheng DX, Kang XN, Wang YX. et al. Periodontal disease and emotional disorders: a meta-analysis. J Clin Periodontol 2021; 48 (02) 180-204
- 51 Peruzzo DC, Benatti BB, Ambrosano GM. et al. A systematic review of stress and psychological factors as possible risk factors for periodontal disease. J Periodontol 2007; 78 (08) 1491-1504
- 52 Li A, Du M, Chen Y. et al. Periodontitis and cognitive impairment in older adults: the mediating role of mitochondrial dysfunction. J Periodontol 2022; 93 (09) 1302-1313
- 53 Guo H, Chang S, Pi X. et al. The effect of periodontitis on dementia and cognitive impairment: a meta-analysis. Int J Environ Res Public Health 2021; 18 (13) 6823
- 54 Wu Z, Xiao C, Chen F, Wang Y, Guo Z. Pulmonary disease and periodontal health: a meta-analysis. Sleep Breath 2022; 26 (04) 1857-1868
- 55 Dziedzic A. Is periodontitis associated with age-related cognitive impairment? The systematic review, confounders assessment and meta-analysis of clinical studies. Int J Mol Sci 2022; 23 (23) 15320
- 56 Usuga-Vacca M, Díaz-Báez D, Beltrán EO, Cortes A, Vargas-Sanchez PK, Avila V. Oral diseases and systemic conditions: correlation analyses from the Colombian national health records between 2016 and 2023. Front Oral Health 2024; 5: 1466427
- 57 Moss ME, Beck JD, Kaplan BH. et al. Exploratory case-control analysis of psychosocial factors and adult periodontitis. J Periodontol 1996; 67 (10 Suppl): 1060-1069
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Article published online:
07 July 2025
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References
- 1 Lutz W, Sanderson W, Scherbov S. The coming acceleration of global population ageing. Nature 2008; 451 (7179): 716-719
- 2 WHO. Trends in maternal mortality 2000 to 2017: estimates by WHO, UNICEF, UNFPA, World Bank Group and the United Nations Population Division: World Health Organization; 2019
- 3 Bongaarts J. Human population growth and the demographic transition. Philos Trans R Soc Lond B Biol Sci 2009; 364 (1532): 2985-2990
- 4 Slade GD, Akinkugbe AA, Sanders AE. Projections of U.S. Edentulism prevalence following 5 decades of decline. J Dent Res 2014; 93 (10) 959-965
- 5 Sepolia S, Verma P. Periodontal oral health in geriatric patients: an observational study. Journal of Advanced Medical and Dental Sciences Research 2020; 8 (11) 223-228
- 6 Solis AC, Lotufo RF, Pannuti CM, Brunheiro EC, Marques AH, Lotufo-Neto F. Association of periodontal disease to anxiety and depression symptoms, and psychosocial stress factors. J Clin Periodontol 2004; 31 (08) 633-638
- 7 Douglass CW, Jette AM, Fox CH. et al. Oral health status of the elderly in New England. J Gerontol 1993; 48 (02) M39-M46
- 8 Armitage GC. Periodontal diagnoses and classification of periodontal diseases. Periodontol 2000 2004; 34 (01) 9-21
- 9 Jin LJ, Armitage GC, Klinge B, Lang NP, Tonetti M, Williams RC. Global oral health inequalities: task group–periodontal disease. Adv Dent Res 2011; 23 (02) 221-226
- 10 Guentsch A, Pfister W, Cachovan G. et al. Oral prophylaxis and its effects on halitosis-associated and inflammatory parameters in patients with chronic periodontitis. Int J Dent Hyg 2014; 12 (03) 199-207
- 11 Kingman A, Albandar JM. Methodological aspects of epidemiological studies of periodontal diseases. Periodontol 2000 2002; 29 (01) 11-30
- 12 Eke PI, Dye BA, Wei L, Thornton-Evans GO, Genco RJ. CDC Periodontal Disease Surveillance workgroup: James Beck (University of North Carolina, Chapel Hill, USA), Gordon Douglass (Past President, American Academy of Periodontology), Roy Page (University of Washington). Prevalence of periodontitis in adults in the United States: 2009 and 2010. J Dent Res 2012; 91 (10) 914-920
- 13 Fox CH, Jette AM, McGuire SM, Feldman HA, Douglass CW. Periodontal disease among New England elders. J Periodontol 1994; 65 (07) 676-684
- 14 Phillips LL, Paukert AL, Stanley MA, Kunik ME. Incorporating religion and spirituality to improve care for anxiety and depression in older adults. Geriatrics 2009; 64 (08) 15-18
- 15 Montero-Aguilar M, Muñoz-Torres F, Elías-Boneta AR, Dye B, Joshipura KJ. High levels of periodontal disease among the older adult population in San Juan, Puerto Rico. Community Dent Health 2012; 29 (03) 224-228
- 16 Nankwanga A, Phillips J, Neema S. Exploring and curbing the effects of HIV/AIDS on elderly people in Uganda. JCHS 2009 4. 02
- 17 Cho SM, Saw YM, Saw TN. et al. Prevalence and risk factors of anxiety and depression among the community-dwelling elderly in Nay Pyi Taw Union Territory, Myanmar. Sci Rep 2021; 11 (01) 9763
- 18 Farsi N, Al Amoudi N, Farsi J, Bokhary S, Sonbul H. Periodontal health and its relationship with salivary factors among different age groups in a Saudi population. Oral Health Prev Dent 2008; 6 (02) 147-154
- 19 Burt BA. Periodontitis and aging: reviewing recent evidence. J Am Dent Assoc 1994; 125 (03) 273-279
- 20 Friedlander AH, Norman DC. Late-life depression: psychopathology, medical interventions, and dental implications. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002; 94 (04) 404-412
- 21 Al-Zahrani MS, Borawski EA, Bissada NF. Periodontitis and three health-enhancing behaviors: maintaining normal weight, engaging in recommended level of exercise, and consuming a high-quality diet. J Periodontol 2005; 76 (08) 1362-1366
- 22 Sanz M, Marco Del Castillo A, Jepsen S. et al. Periodontitis and cardiovascular diseases: consensus report. J Clin Periodontol 2020; 47 (03) 268-288
- 23 Ramseier CA, Klima S, Klima E, Enkling N. Dental anxiety in Switzerland: trends in prevalence and associations with socioeconomic factors in 2010 and 2017. Swiss Dent J 2023; 134 (01) 52-71
- 24 Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009; 151 (04) 264-269 , W64
- 25 Margulis AV, Pladevall M, Riera-Guardia N. et al. Quality assessment of observational studies in a drug-safety systematic review, comparison of two tools: the Newcastle-Ottawa Scale and the RTI item bank. Clin Epidemiol 2014; 6: 359-368
- 26 Viana LRF, Castro CP, Pereira H-BW, Pereira AdFV, Lopes FF. Is depression associated with periodontal status in elderly?. Braz J Oral Sci 2013; 12: 20-22
- 27 Iwasaki M, Yoshihara A, Kimura Y. et al. Longitudinal relationship of severe periodontitis with cognitive decline in older Japanese. J Periodontal Res 2016; 51 (05) 681-688
- 28 Kim YR, Son M, Nam SH. Association between depressive mood and chronic periodontitis among senior residents using the National Health Insurance Service-Senior Cohort Database. J Periodontol 2023; 94 (06) 742-750
- 29 Persson GR, Persson RE, MacEntee CI, Wyatt CC, Hollender LG, Kiyak HA. Periodontitis and perceived risk for periodontitis in elders with evidence of depression. J Clin Periodontol 2003; 30 (08) 691-696
- 30 Skośkiewicz-Malinowska K, Malicka B, Ziętek M, Kaczmarek U. Oral health condition and occurrence of depression in the elderly. Medicine (Baltimore) 2018; 97 (41) e12490
- 31 Youn H-Y, Shin H-E, Cho M-J. Association of sleep duration and depression with periodontitis in older people aged 65 years and older. J Dental Hygiene Science 2019; 19 (03) 205-212
- 32 Luca M, Luca A, Grasso CMAV, Calandra C. Nothing to smile about. Neuropsychiatr Dis Treat 2014; 10: 1999-2008
- 33 Kjellström B, Gustafsson A, Nordendal E. et al; PAROKRANK Steering Committee. Symptoms of depression and their relation to myocardial infarction and periodontitis. Eur J Cardiovasc Nurs 2017; 16 (06) 468-474
- 34 Botelho J, Machado V, Proença L. et al. Perceived xerostomia, stress and periodontal status impact on elderly oral health-related quality of life: findings from a cross-sectional survey. BMC Oral Health 2020; 20 (01) 199
- 35 Hilgert JB, Hugo FN, Bandeira DR, Bozzetti MC. Stress, cortisol, and periodontitis in a population aged 50 years and over. J Dent Res 2006; 85 (04) 324-328
- 36 Coelho JMF, Miranda SS, da Cruz SS. et al. Is there association between stress and periodontitis?. Clin Oral Investig 2020; 24 (07) 2285-2294
- 37 Shin HS, Shin MS, Ahn YB, Choi BY, Nam JH, Kim HD. Periodontitis is associated with cognitive impairment in elderly Koreans: results from the Yangpyeong Cohort Study. J Am Geriatr Soc 2016; 64 (01) 162-167
- 38 Hugo FN, Hilgert JB, Bozzetti MC. et al. Chronic stress, depression, and cortisol levels as risk indicators of elevated plaque and gingivitis levels in individuals aged 50 years and older. J Periodontol 2006; 77 (06) 1008-1014
- 39 Sutherland SE. Evidence-based dentistry: Part IV. Research design and levels of evidence. J Can Dent Assoc 2001; 67 (07) 375-378
- 40 Cadden SW. Orofacial pain. Guidelines for assessment, diagnosis, and management, 4th edition (2008). Eur J Orthod 2009; 31 (02) 216-217
- 41 Cademartori MG, Gastal MT, Nascimento GG, Demarco FF, Corrêa MB. Is depression associated with oral health outcomes in adults and elders? A systematic review and meta-analysis. Clin Oral Investig 2018; 22 (08) 2685-2702
- 42 Allan CE, Valkanova V, Ebmeier KP. Depression in older people is underdiagnosed. Practitioner 2014; 258 (1771): 19-22 , 2–3
- 43 Bentley SM, Pagalilauan GL, Simpson SA. Major depression. Med Clin North Am 2014; 98 (05) 981-1005
- 44 Haas AN, Gaio EJ, Oppermann RV, Rösing CK, Albandar JM, Susin C. Pattern and rate of progression of periodontal attachment loss in an urban population of South Brazil: a 5-years population-based prospective study. J Clin Periodontol 2012; 39 (01) 1-9
- 45 Subramanian AK, Narayan V, Navaneethan R. Oxidative Stress and Oral Diseases. In: Maurya PK, Dua K. eds. Role of Oxidative Stress in Pathophysiology of Diseases. Singapore: Springer; 2020: 1-12
- 46 Tong D, Dawson J, Love R. Factors affecting oral health status in an elderly military veteran population in New Zealand. J Mil Veterans Health 2010; 18 (03) 12-17
- 47 Dumitrescu AL. Depression and inflammatory periodontal disease considerations - an interdisciplinary approach. Front Psychol 2016; 7: 347
- 48 Arias-Bujanda N, Regueira-Iglesias A, Balsa-Castro C, Nibali L, Donos N, Tomás I. Accuracy of single molecular biomarkers in saliva for the diagnosis of periodontitis: a systematic review and meta-analysis. J Clin Periodontol 2020; 47 (01) 2-18
- 49 Belvederi Murri M, Pariante C, Mondelli V. et al. HPA axis and aging in depression: systematic review and meta-analysis. Psychoneuroendocrinology 2014; 41: 46-62
- 50 Zheng DX, Kang XN, Wang YX. et al. Periodontal disease and emotional disorders: a meta-analysis. J Clin Periodontol 2021; 48 (02) 180-204
- 51 Peruzzo DC, Benatti BB, Ambrosano GM. et al. A systematic review of stress and psychological factors as possible risk factors for periodontal disease. J Periodontol 2007; 78 (08) 1491-1504
- 52 Li A, Du M, Chen Y. et al. Periodontitis and cognitive impairment in older adults: the mediating role of mitochondrial dysfunction. J Periodontol 2022; 93 (09) 1302-1313
- 53 Guo H, Chang S, Pi X. et al. The effect of periodontitis on dementia and cognitive impairment: a meta-analysis. Int J Environ Res Public Health 2021; 18 (13) 6823
- 54 Wu Z, Xiao C, Chen F, Wang Y, Guo Z. Pulmonary disease and periodontal health: a meta-analysis. Sleep Breath 2022; 26 (04) 1857-1868
- 55 Dziedzic A. Is periodontitis associated with age-related cognitive impairment? The systematic review, confounders assessment and meta-analysis of clinical studies. Int J Mol Sci 2022; 23 (23) 15320
- 56 Usuga-Vacca M, Díaz-Báez D, Beltrán EO, Cortes A, Vargas-Sanchez PK, Avila V. Oral diseases and systemic conditions: correlation analyses from the Colombian national health records between 2016 and 2023. Front Oral Health 2024; 5: 1466427
- 57 Moss ME, Beck JD, Kaplan BH. et al. Exploratory case-control analysis of psychosocial factors and adult periodontitis. J Periodontol 1996; 67 (10 Suppl): 1060-1069

