4.6 Article

DNA methylation outlier burden, health, and ageing in Generation Scotland and the Lothian Birth Cohorts of 1921 and 1936

Journal

CLINICAL EPIGENETICS
Volume 12, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13148-020-00838-0

Keywords

Ageing; Epigenetics; Stochastic epigenetic mutations; Epigenetic outliers; Survival; Generation Scotland; Lothian Birth Cohorts

Funding

  1. Chief Scientist Office of the Scottish Government Health Directorates [CZD/16/6]
  2. Scottish Funding Council [HR03006]
  3. Medical Research Council UK [104036/Z/14/Z]
  4. Wellcome Trust [108890/Z/15/Z]
  5. UK's Biotechnology and Biological Sciences Research Council (BBSRC)
  6. Royal Society-Wolfson Research Merit Award
  7. Chief Scientist Office (CSO) of the Scottish Government's Health Directorates
  8. Age UK (Disconnected Mind program)
  9. Medical Research Council [MR/M01311/1, MR/K026992/1]
  10. Centre for Cognitive Ageing and Cognitive Epidemiology (Pilot Fund award)
  11. Wellcome Trust Institutional Strategic Support Fund
  12. University of Edinburgh
  13. University of Queensland
  14. Age UK
  15. Biotechnology and Biological Sciences Research Council [MR/K026992/1]
  16. University of Edinburgh College of Medicine and Veterinary Medicine
  17. Alzheimer's Research UK [ARUK-PG2017B-10]
  18. Loo and Hans Osterman Foundation
  19. Foundation for Geriatric Diseases
  20. Magnus Bergwall Foundation
  21. Foundation Gamla Tjanarinnor
  22. Erik Ronnberg award for scientific studies on ageing and age-related diseases
  23. King Gustaf Vs and Queen Victorias Freemanson Foundation for aging studies
  24. Karolinska Institutet (Strategic Research Area in Epidemiology, KID)
  25. Swedish Research Council [2015-03255]
  26. Swedish Council for Working Life and Social Research (FORTE) [2013-2292]
  27. MRC [G0700704] Funding Source: UKRI

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Background DNA methylation outlier burden has been suggested as a potential marker of biological age. An outlier is typically defined as DNA methylation levels at any one CpG site that are three times beyond the inter-quartile range from the 25th or 75th percentiles compared to the rest of the population. DNA methylation outlier burden (the number of such outlier sites per individual) increases exponentially with age. However, these findings have been observed in small samples. Results Here, we showed an association between age and log(10)-transformed DNA methylation outlier burden in a large cross-sectional cohort, the Generation Scotland Family Health Study (N = 7010, beta = 0.0091, p < 2 x 10(-16)), and in two longitudinal cohort studies, the Lothian Birth Cohorts of 1921 (N = 430, beta = 0.033, p = 7.9 x 10(-4)) and 1936 (N = 898, beta = 0.0079, p = 0.074). Significant confounders of both cross-sectional and longitudinal associations between outlier burden and age included white blood cell proportions, body mass index (BMI), smoking, and batch effects. In Generation Scotland, the increase in epigenetic outlier burden with age was not purely an artefact of an increase in DNA methylation level variability with age (epigenetic drift). Log(10)-transformed DNA methylation outlier burden in Generation Scotland was not related to self-reported, or family history of, age-related diseases, and it was not heritable (SNP-based heritability of 4.4%, p = 0.18). Finally, DNA methylation outlier burden was not significantly related to survival in either of the Lothian Birth Cohorts individually or in the meta-analysis after correction for multiple testing (HRmeta = 1.12; 95% CImeta = [1.02; 1.21]; p(meta) = 0.021). Conclusions These findings suggest that, while it does not associate with ageing-related health outcomes, DNA methylation outlier burden does track chronological ageing and may also relate to survival. DNA methylation outlier burden may thus be useful as a marker of biological ageing.

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