| Literature DB >> 34227900 |
Lauren L Schmitz1, Wei Zhao2, Scott M Ratliff2, Julia Goodwin3, Jiacheng Miao4, Qiongshi Lu4,5, Xiuqing Guo6, Kent D Taylor6, Jingzhong Ding7, Yongmei Liu8, Morgan Levine9, Jennifer A Smith2,10.
Abstract
Epigenetic clocks have been widely used to predict disease risk in multiple tissues or cells. Their success as a measure of biological ageing has prompted research on the connection between epigenetic pathways of ageing and the socioeconomic gradient in health and mortality. However, studies examining social correlates of epigenetic ageing have yielded inconsistent results. We conducted a comprehensive, comparative analysis of associations between various dimensions of socioeconomic status (SES) (education, income, wealth, occupation, neighbourhood environment, and childhood SES) and eight epigenetic clocks in two well-powered US ageing studies: The Multi-Ethnic Study of Atherosclerosis (MESA) (n = 1,211) and the Health and Retirement Study (HRS) (n = 4,018). In both studies, we found robust associations between SES measures in adulthood and the GrimAge and DunedinPoAm clocks (Bonferroni-corrected p-value < 0.01). In the HRS, significant associations with the Levine and Yang clocks were also evident. These associations were only partially mediated by smoking, alcohol consumption, and obesity, which suggests that differences in health behaviours alone cannot explain the SES gradient in epigenetic ageing in older adults. Further analyses revealed concurrent associations between polygenic risk for accelerated intrinsic epigenetic ageing, SES, and the Levine clock, indicating that genetic risk and social disadvantage may contribute additively to faster biological aging.Entities:
Keywords: DNA methylation age; epigenetic clock; polygenic score; socioeconomic status
Mesh:
Year: 2021 PMID: 34227900 PMCID: PMC9235889 DOI: 10.1080/15592294.2021.1939479
Source DB: PubMed Journal: Epigenetics ISSN: 1559-2294 Impact factor: 4.861