Psychological adversities and epigenetic ageing in midlife and older age: A systematic review and meta-analysis.

J Prev Alzheimers DisAug 7, 2026 (epub)

Jiuyu Guo, Jiatong Shan, Kaisy Xinhong Ye et al.

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In 30 seconds

This systematic review and meta-analysis examined associations between psychological adversities and epigenetic age acceleration (EAA) from midlife onward. It included 22 studies, 15 rated high quality, and used random-effects models. Across studies, psychological adversities were consistently positively associated with second-generation epigenetic clocks. Greater loneliness (β = 0.07, 95 % CI [0.06, 0.08]), depression (β = 0.08, 95 % CI [0.04, 0.13]), and stress (β = 0.10, 95 % CI [0.03, 0.16]) were each associated with higher EAA.

Key findings

  • Greater loneliness was associated with higher EAA (β = 0.07, 95 % CI [0.06, 0.08], I 2 = 0 %, p = 0.002).
  • Depression was associated with higher EAA (β = 0.08, 95 % CI [0.04, 0.13], I 2 = 55.2 %, p = 0.003).
  • Stress was associated with higher EAA (β = 0.10, 95 % CI [0.03, 0.16], I2 = 68.4 %, p = 0.009).
  • Positive associations across adversity types were consistently observed for the second-generation PhenoAge and GrimAge clocks.

Why it matters

The findings link common psychosocial adversities with epigenetic measures of ageing in midlife and older populations. This supports considering psychological and social exposures when studying biological ageing and health across the life course. The associations do not establish that adversity causes accelerated ageing, or that reducing adversity would slow it.

What to keep in mind

The review found no studies examining anxiety and noted underrepresentation of non-Western populations. Heterogeneity was substantial for the depression and stress meta-analyses.

Source

Published in J Prev Alzheimers Dis. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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