4.5 Article

Comparison of DNA methylation clocks in black South African men

期刊

EPIGENOMICS
卷 13, 期 6, 页码 437-450

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/epi-2020-0333

关键词

biological age; GrimAge; PhenoAge; phenotypic age; smoking

资金

  1. North-West University
  2. South African National Research Foundation
  3. Population Health Research Institute
  4. South African Medical Research Council
  5. NorthWest Province Health Department
  6. South African Netherlands Partnerships in Development
  7. Academy of Medical Sciences UK (Newton Fund Advanced Fellowship Grant)
  8. South African National Research Foundation [SFH106264, MND121094]
  9. Novo Nordisk Fonden Challenge Programme: Harnessing the Power of Big Data to Address the Societal Challenge of Aging [NNF17OC0027812]
  10. Medical Research Council [MC UU 00011/5]
  11. University of Bristol [MC UU 00011/5]
  12. MRC [MC_UU_00011/5] Funding Source: UKRI

向作者/读者索取更多资源

This study investigated five DNA methylation clocks in 120 older black South African men and found that these clocks tend to underestimate the biological age of older individuals. GrimAge more accurately characterizes biological decline in this African cohort compared with PhenoAge, highlighting the importance of studying under-represented populations for robust and useful methylation-derived indicators in all populations.
Aims: DNA methylation clocks are widely used to estimate biological age, although limited data are available on non-European ethnicities. This manuscript characterizes the behavior of five DNA methylation clocks in 120 older black South African men. Methods: The age estimation accuracy of the Horvath, Hannum and skin and blood clocks and the relative age-related mortality risk and predicted time to death portrayed by the PhenoAge and GrimAge biomarkers are investigated, respectively. Results: The results confirm the tendency of DNA methylation clocks to underestimate the biological age of older individuals. GrimAge more accurately characterizes biological decline in this African cohort compared with PhenoAge owing to the unique inclusion of smoking-related damage in the GrimAge estimate. Conclusions: Each clock provides a different fraction of information regarding the aging body. It is essential to continue studying under-represented population groups to ensure methylation-derived indicators are robust and useful in all populations.

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