The Journal of Prevention of Alzheimer's Disease
Psychological adversities and epigenetic ageing in midlife and older age: A systematic review and meta-analysis
By Jiuyu Guo, Jiatong Shan, Kaisy Xinhong Ye and 7 others.
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The Journal of Prevention of Alzheimer's Disease
By Jiuyu Guo, Jiatong Shan, Kaisy Xinhong Ye and 7 others.
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Epigenetic modification is a hallmark of aging that encloses physiological information relevant to health and longevity and has been used to construct epigenetic clocks that estimate epigenetic age acceleration (EAA) to monitor population health across the life span. Psychological adversities (PA) are recognized contributors to poor health; however, their potential role in EAA remains insufficiently understood in older adults.
This study systematically reviews and meta-analyzes the association between PA and EAA from midlife onward.
Eligible literatures were indexed in five databases up to July 2025. Study quality was assessed using an adapted Newcastle-Ottawa scale. Meta-analyses were performed using random-effects models, followed by post hoc and sensitivity analyses to assess robustness.
Twenty-two studies were included, of which fifteen were classified as high quality. Irrespective of the type of psychological adversity, positive associations were consistently observed for second-generation epigenetic clocks (PhenoAge and GrimAge). Meta-analyses revealed that greater loneliness (β = 0.07, 95 % CI [0.06, 0.08], I 2 = 0 %, p = 0.002), depression (β = 0.08, 95 % CI [0.04, 0.13], I 2 = 55.2 %, p = 0.003), and stress (β = 0.10, 95 % CI [0.03, 0.16], I2 = 68.4 %, p = 0.009) were each associated with higher EAA.
Psychosocial stress, depression, and loneliness are each associated with accelerated aging from midlife onward. Notable gaps include the lack of studies examining anxiety and underrepresentation of non-Western population. Whether alleviating psychological adversities translates into decelerated aging trajectories requests future intervention studies.
Published in The Journal of Prevention of Alzheimer's Disease. The abstract is shown as published and remains the work of its authors; read the full article at the source.
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