4.7 Article

Epigenome-wide Association Study Analysis of Calorie Restriction in Humans, CALERIE™ Trial Analysis

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/gerona/glac168

关键词

Caloric restriction; Epigenome; Human aging

资金

  1. National Institute on Aging Grant [R01AG061378]
  2. National Institute of Aging Grant [R33AG070455]
  3. National Institute of Health [R01AG054840, P30-AG028716]
  4. McKnight Scholar Award from the McKnight Brain Research Foundation through the American Brain Foundation
  5. American Academy of Neurology

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Calorie restriction has been shown to increase healthy lifespan and slow down aging-associated DNA methylation changes. A study conducted in humans found that calorie restriction can alter age-related DNA methylation patterns but no significant changes were observed at individual CpG sites.
Calorie restriction (CR) increases healthy life span and is accompanied by slowing or reversal of aging-associated DNA methylation (DNAm) changes in animal models. In the Comprehensive Assessment of Long-term Effects of Reducing Intake of Energy (CALERIE (TM)) human trial, we evaluated associations of CR and changes in whole-blood DNAm. CALERIE (TM) randomized 220 healthy, nonobese adults in a 2:1 allocation to 2 years of CR or ad libitum (AL) diet. The average CR in the treatment group through 24 months of follow-up was 12%. Whole blood (baseline, 12, and 24 months) DNAm profiles were measured. Epigenome-wide association study (EWAS) analysis tested CR-induced changes from baseline to 12 and 24 months in the n = 197 participants with available DNAm data. CR treatment was not associated with epigenome-wide significant (false discovery rate [FDR] < 0.05) DNAm changes at the individual-CpG-site level. Secondary analysis of sets of CpG sites identified in published EWAS revealed that CR induced DNAm changes opposite to those associated with higher body mass index and cigarette smoking (p < .003 at 12- and 24-month follow-ups). In contrast, CR altered DNAm at chronological-age-associated CpG sites in the direction of older age (p < .003 at 12- and 24-month follow-ups). Although individual CpG site DNAm changes in response to CR were not identified, analyses of sets CpGs identified in prior EWAS revealed CR-induced changes to blood DNAm. Altered CpG sets were enriched for insulin production, glucose tolerance, inflammation, and DNA-binding and DNA-regulation pathways, several of which are known to be modified by CR. DNAm changes may contribute to CR effects on aging.

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