Early life adversity and age acceleration at mid-life and older ages indexed using the next-generation GrimAge and Pace of Aging epigenetic clocks.
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McCrory C, Fiorito G, O'Halloran AM, Polidoro S, Vineis P, Kenny RA., Early life adversity and age acceleration at mid-life and older ages indexed using the next-generation GrimAge and Pace of Aging epigenetic clocks., Psychoneuroendocrinology, 137, 2021, 105643
Abstract
Objective: This retrospective cross-sectional study was designed to explore whether the experience of childhood
adversity was associated with epigenetic age acceleration in mid-life and older ages using the next generation
GrimAge and Pace of Aging DNA methylation clocks.
Method: The study involved a sub-sample of 490 individuals aged 50–87 years of age participating in the Irish
Longitudinal Study on Aging (TILDA); a large nationally representative prospective cohort study of aging in
Ireland. Childhood adversity was ascertained via self-report using 5-items that were deemed to indicate
potentially nefarious childhood exposures, including growing up poor, death of a parent, parental substance
abuse in the family, childhood physical abuse, and childhood sexual abuse.
Results: Only childhood poverty was associated with significant epigenetic age acceleration according to the
GrimAge and Pace of Aging clocks, hastening biological aging by 2.04 years [CI= 1.07, 3.00; p < 0.001] and 1.16
years [CI= 0.11, 2.21; p = 0.030] respectively. Analysis of the dose-response pattern revealed each additional
adversity was associated with 0.69 years of age acceleration [CI= 0.23, 1.15; p = 0.004] according to the
GrimAge clock. Mediation analysis suggested that lifetime smoking explains a substantial portion (>50%) of the
excess risk of age acceleration amongst those who experienced childhood poverty.
Conclusions: This study adds to the growing body of evidence which implicates early life adversity, particularly
deprivation as a potential precipitant of earlier biological aging, and implicates smoking-related changes to DNA
methylation processes as a candidate pathway and mechanism through which the social environment gets
transduced at a biological level to hasten the aging process.
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Author's Homepage: http://people.tcd.ie/mccrorc
Type of material: Journal Article

