Bidirectional relationship between epigenetic age and stroke, dementia, and late-life depression

Chronological age is an imperfect estimate of molecular aging. Epigenetic age, derived from DNA methylation data, provides a more nuanced representation of aging-related biological processes. We examine the bidirectional relationship between epigenetic age and brain health events (stroke, dementia, late-life depression) using data from 4,018 participants. Participants with a prior brain health event are 4% epigenetically older (β = 0.04, SE = 0.01), indicating these conditions are associated with accelerated aging beyond that captured by chronological age. Additionally, a one standard deviation increase in epigenetic age is associated with 70% higher odds of experiencing a brain health event in the next four years (OR = 1.70, 95% CI = 1.16-2.50), suggesting epigenetic age acceleration is not just a consequence but also a predictor of poor brain health. Mendelian Randomization analyses replicate these findings, supporting their causal nature. Our results support using epigenetic age as a biomarker to evaluate interventions aimed at preventing and promoting recovery after brain health events.

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Publication Details

Journal
Nature Communications
Published
2025-02-01
DOI
https://doi.org/10.1038/s41467-024-54721-0
Citations
9
Primary Topic
Birth, Development, and Health
Type
article
Field-Weighted Citation Impact
31.45

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article

Bidirectional relationship between epigenetic age and stroke, dementia, and late-life depression

Shufan Huo, Thomas M. Gill, Cyprien Rivier, Guido J. Falcone et al.
9 citations
Nature Communications
Birth, Development, and Health
31.45
article

Bidirectional relationship between epigenetic age and stroke, dementia, and late-life depression

Shufan Huo, Thomas M. Gill, Cyprien Rivier, Guido J. Falcone, Adam de Havenon, Kevin Navin Sheth, Daniela Renedo, Santiago Clocchiatti‐Tuozzo, Natalia Szejko, Hongyu Zhao
article en
9 citations

Abstract

Chronological age is an imperfect estimate of molecular aging. Epigenetic age, derived from DNA methylation data, provides a more nuanced representation of aging-related biological processes. We examine the bidirectional relationship between epigenetic age and brain health events (stroke, dementia, late-life depression) using data from 4,018 participants. Participants with a prior brain health event are 4% epigenetically older (β = 0.04, SE = 0.01), indicating these conditions are associated with accelerated aging beyond that captured by chronological age. Additionally, a one standard deviation increase in epigenetic age is associated with 70% higher odds of experiencing a brain health event in the next four years (OR = 1.70, 95% CI = 1.16-2.50), suggesting epigenetic age acceleration is not just a consequence but also a predictor of poor brain health. Mendelian Randomization analyses replicate these findings, supporting their causal nature. Our results support using epigenetic age as a biomarker to evaluate interventions aimed at preventing and promoting recovery after brain health events.

Nature CommunicationsVol. 16(1)
University of Calgary (CA), Medical University of Warsaw (PL), Yale University (US), Yale New Haven Health System (US)
American Heart Association, Yale University, American Brain Foundation, Biogen, Tourette Association of America, Deutsche Forschungsgemeinschaft, Warszawski Uniwersytet Medyczny, Uniwersytet Warszawski, Ministerstwo Zdrowia, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke
No poverty
Openalex Percentile: Top 0%
Birth, Development, and Health
31.45
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