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Article: Biological aging mediates the association between periodontitis and cardiovascular disease: results from a national population study and Mendelian randomization analysis

TitleBiological aging mediates the association between periodontitis and cardiovascular disease: results from a national population study and Mendelian randomization analysis
Authors
KeywordsBiological aging
Cardiovascular disease
Causal association
Mediating effect
Periodontitis
Issue Date24-Aug-2024
PublisherBioMed Central
Citation
Clinical Epigenetics, 2024, v. 16, n. 1 How to Cite?
AbstractBackground: The relationship between periodontitis and cardiovascular disease (CVD) has been extensively studied, but the role of biological aging in this relationship remains poorly understood. This study is dedicated to investigating the effect of periodontitis on the incidence of CVD and to elucidating the potential mediating role of biological aging. Furthermore, this study will seek to elucidate the causal association between periodontitis, CVD, and biological aging. Methods: We included 3269 participants from the National Health and Nutrition Examination Survey (2009–2014) with diagnostic information on periodontitis and composite CVD events. Biological aging was evaluated by utilizing both the Klemera–Doubal method’s calculated biological age (KDMAge) and phenotypic age (PhenoAge). Logistic regression, restricted cubic spline (RCS) analysis, and subgroup analysis were used for data analysis. Mediation analysis was employed to explore the mediating role of biological aging. Subsequently, Mendelian randomization (MR) analyses were performed using genome-wide association study databases to explore potential causal relationships between periodontitis, CVD, and biological aging. Results: Periodontitis was associated with a higher risk of CVD. Participants with periodontitis were found to have increased levels of biological aging, and elevated levels of biological aging were associated with increased CVD risk. Mediation analyses showed a partial mediating effect of biological aging (PhenoAge: 44.6%; KDMAge: 22.9%) between periodontitis and CVD risk. MR analysis showed that periodontitis played a causal role in increasing the risk of small vessel stroke, while myocardial infarction was found to increase the risk of periodontitis. In addition, reverse MR analysis showed that phenotypic aging can increase the risk of periodontitis, and there is a two-way causal relationship between CVD and biological aging. Conclusions: Periodontitis is associated with an increased CVD risk, partially mediated by biological aging, with a complex causal interrelationship. Targeted interventions for periodontal health may slow the biological aging processes and reduce CVD risk.
Persistent Identifierhttp://hdl.handle.net/10722/347957
ISSN
2023 Impact Factor: 4.8
2023 SCImago Journal Rankings: 1.727

 

DC FieldValueLanguage
dc.contributor.authorZhang, Zhaoqi-
dc.contributor.authorZhao, Xingru-
dc.contributor.authorGao, Shang-
dc.contributor.authorLi, An-
dc.contributor.authorDeng, Ke-
dc.contributor.authorYang, Kai-
dc.contributor.authorLiu, Wei-
dc.contributor.authorDu, Mi-
dc.date.accessioned2024-10-03T00:30:44Z-
dc.date.available2024-10-03T00:30:44Z-
dc.date.issued2024-08-24-
dc.identifier.citationClinical Epigenetics, 2024, v. 16, n. 1-
dc.identifier.issn1868-7075-
dc.identifier.urihttp://hdl.handle.net/10722/347957-
dc.description.abstractBackground: The relationship between periodontitis and cardiovascular disease (CVD) has been extensively studied, but the role of biological aging in this relationship remains poorly understood. This study is dedicated to investigating the effect of periodontitis on the incidence of CVD and to elucidating the potential mediating role of biological aging. Furthermore, this study will seek to elucidate the causal association between periodontitis, CVD, and biological aging. Methods: We included 3269 participants from the National Health and Nutrition Examination Survey (2009–2014) with diagnostic information on periodontitis and composite CVD events. Biological aging was evaluated by utilizing both the Klemera–Doubal method’s calculated biological age (KDMAge) and phenotypic age (PhenoAge). Logistic regression, restricted cubic spline (RCS) analysis, and subgroup analysis were used for data analysis. Mediation analysis was employed to explore the mediating role of biological aging. Subsequently, Mendelian randomization (MR) analyses were performed using genome-wide association study databases to explore potential causal relationships between periodontitis, CVD, and biological aging. Results: Periodontitis was associated with a higher risk of CVD. Participants with periodontitis were found to have increased levels of biological aging, and elevated levels of biological aging were associated with increased CVD risk. Mediation analyses showed a partial mediating effect of biological aging (PhenoAge: 44.6%; KDMAge: 22.9%) between periodontitis and CVD risk. MR analysis showed that periodontitis played a causal role in increasing the risk of small vessel stroke, while myocardial infarction was found to increase the risk of periodontitis. In addition, reverse MR analysis showed that phenotypic aging can increase the risk of periodontitis, and there is a two-way causal relationship between CVD and biological aging. Conclusions: Periodontitis is associated with an increased CVD risk, partially mediated by biological aging, with a complex causal interrelationship. Targeted interventions for periodontal health may slow the biological aging processes and reduce CVD risk.-
dc.languageeng-
dc.publisherBioMed Central-
dc.relation.ispartofClinical Epigenetics-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBiological aging-
dc.subjectCardiovascular disease-
dc.subjectCausal association-
dc.subjectMediating effect-
dc.subjectPeriodontitis-
dc.titleBiological aging mediates the association between periodontitis and cardiovascular disease: results from a national population study and Mendelian randomization analysis-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13148-024-01732-9-
dc.identifier.scopuseid_2-s2.0-85201966472-
dc.identifier.volume16-
dc.identifier.issue1-
dc.identifier.eissn1868-7083-
dc.identifier.issnl1868-7075-

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