4.6 Article

Epigenetic Aging in Major Depressive Disorder

期刊

AMERICAN JOURNAL OF PSYCHIATRY
卷 175, 期 8, 页码 774-782

出版社

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2018.17060595

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资金

  1. Geestkracht program of the Netherlands Organization for Health Research and Development (Zon-MW) [10-000-1002]
  2. VU University Medical Center
  3. GGZ in Geest
  4. Arkin
  5. Leiden University Medical Center
  6. GGZ Rivierduinen
  7. University Medical Center Groningen
  8. Lentis
  9. GGZ Friesland
  10. GGZ Drenthe
  11. NIMH [R01MH099110]
  12. EMGO+ Travel Grant
  13. Florey Institute of Neuroscience and Mental Health
  14. Alfred and Victorian Forensic Institute of Medicine
  15. Australia's National Health and Medical Research Council
  16. Parkinson's Victoria
  17. Stanley Medical Research Institute
  18. Netherlands Brain Bank
  19. Netherlands Institute of Neuroscience, Amsterdam
  20. Harvard Brain Tissue Resource Center
  21. Janssen Research
  22. Boehringer Ingelheim

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Objective: Major depressive disorder is associated with an increased risk of mortality and aging-related diseases. The authors examined whether major depression is associated with higher epigenetic aging in blood as measured by DNA methylation (DNAm) patterns, whether clinical characteristics of major depression have a further impact on these patterns, and whether the findings replicate in brain tissue. Method: DNAmage was estimated using all methylation sites in blood of 811 depressed patients and 319 control subjects with no lifetime psychiatric disorders and low depressive symptoms from the Netherlands Study of Depression and Anxiety. The residuals of the DNAm age estimates regressed on chronological age were calculated to indicate epigenetic aging. Major depression diagnosis and clinical characteristics were assessed with questionnaires and psychiatric interviews. Analyses were adjusted for sociodemographic characteristics, lifestyle, and health status. Postmortem brain samples of 74 depressed patients and 64 control subjects were used for replication. Pathway enrichment analysis was conducted using Consensus PathDB to gain insight into the biological processes underlying epigenetic aging in blood and brain. Results: Significantly higher epigenetic aging was observed in patients with major depression compared with control subjects (Cohen's d=0.18), with a significant dose effect with increasing symptom severity in the overall sample. In the depression group, epigenetic aging was positively and significantly associated with childhood trauma score. The case-control difference was replicated in an independent data set of postmortem brain samples. The top significantly enriched Gene Ontology terms included neuronal processes. Conclusions: As compared with control subjects, patients with major depression exhibited higher epigenetic aging in blood and brain tissue, suggesting that they are biologically older than their corresponding chronological age. This effect was even more profound in the presence of childhood trauma.

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