Epigenome-wide association study of long-term psychosocial stress in older adults

Lauren A. Opsasnick*, Wei Zhao, Lauren L. Schmitz, Scott M. Ratliff, Jessica D. Faul, Xiang Zhou, Belinda L. Needham, Jennifer A. Smith

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Long-term psychosocial stress is strongly associated with negative physical and mental health outcomes, as well as adverse health behaviours; however, little is known about the role that stress plays on the epigenome. One proposed mechanism by which stress affects DNA methylation is through health behaviours. We conducted an epigenome-wide association study (EWAS) of cumulative psychosocial stress (n = 2,689) from the Health and Retirement Study (mean age = 70.4 years), assessing DNA methylation (Illumina Infinium HumanMethylationEPIC Beadchip) at 789,656 CpG sites. For identified CpG sites, we conducted a formal mediation analysis to examine whether smoking, alcohol use, physical activity, and body mass index (BMI) mediate the relationship between stress and DNA methylation. Nine CpG sites were associated with psychosocial stress (all p < 9E–07; FDR q < 0.10). Additionally, health behaviours and/or BMI mediated 9.4% to 21.8% of the relationship between stress and methylation at eight of the nine CpGs. Several of the identified CpGs were in or near genes associated with cardiometabolic traits, psychosocial disorders, inflammation, and smoking. These findings support our hypothesis that psychosocial stress is associated with DNA methylation across the epigenome. Furthermore, specific health behaviours mediate only a modest percentage of this relationship, providing evidence that other mechanisms may link stress and DNA methylation.

Original languageEnglish (US)
Article number2323907
JournalEpigenetics
Volume19
Issue number1
DOIs
StatePublished - 2024

Funding

This research was funded by the following awards from the National Institute on Aging (NIA): U01 AG009740 (Health and Retirement Study) and R00 AG056599 (Schmitz). This analysis was supported by the National Heart Lung and Blood Institute (NHLBI, R01 HL141292 (Smith)) and National Human Genome Research Institute (NHRGI, T32 HG000040 (Opsasnick)).

Keywords

  • DNA methylation
  • epigenome-wide association study
  • health behaviours
  • mediation analysis
  • psychosocial stress
  • Social epigenomics

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research

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