Autor: |
Freilich CD; Department of Psychology, University of Minnesota Twin Cities., Markon KE; Department of Psychology, University of Minnesota Twin Cities., Cole SW; Department of Psychiatry and Biobehavioral Sciences and Medicine, University of California, Los Angeles., Krueger RF; Department of Psychology, University of Minnesota Twin Cities. |
Jazyk: |
angličtina |
Zdroj: |
Psychology and aging [Psychol Aging] 2024 Jun; Vol. 39 (4), pp. 337-349. Date of Electronic Publication: 2024 Apr 18. |
DOI: |
10.1037/pag0000822 |
Abstrakt: |
Having associations with a range of adverse physical health outcomes including mortality, loneliness is increasingly recognized as a pressing public health concern, but the mechanisms studied to date do not yet explain all loneliness-related health risk. We sought to evaluate whether epigenetic influences on DNA methylation could help explain the relationship between loneliness and health. To do so, we first estimated associations between loneliness and epigenetic age acceleration (EAA) in a subsample of participants in the study of midlife in the United States ( n = 1,310), before testing whether EAA mediated and/or moderated the association between loneliness and the onset of chronic health conditions in older adulthood ( n = 445 completing longitudinal follow-ups). Greater loneliness was weakly associated with greater EAA in the Horvath, DunedinPACE, and GrimAge measures after accounting for demographic (0.08 ≤ β ≤ 0.11) and behavioral (0.06 ≤ β ≤ 0.08) covariates. Loneliness also predicted increases in chronic condition counts and these effects were more pronounced for individuals with higher DunedinPACE EAA values (interaction term β = 0.09, p = .009), suggesting possible synergistic impacts. EAA measures appear to be promising in helping to understand individual variations in the health impacts of loneliness, but the specific mechanisms involved require further research. (PsycInfo Database Record (c) 2024 APA, all rights reserved). |
Databáze: |
MEDLINE |
Externí odkaz: |
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