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Fiorito, G.* ; Pedron, S. ; Ochoa-Rosales, C.* ; McCrory, C.* ; Polidoro, S.* ; Zhang, Y.* ; Dugué, P.A.* ; Ratliff, S.* ; Zhao, W.N.* ; Mckay, G.J.* ; Costa, G.* ; Solinas, M.G.* ; Mullan Harris, K.* ; Tumino, R.* ; Grioni, S.* ; Ricceri, F.* ; Panico, S.* ; Brenner, H.* ; Schwettmann, L. ; Waldenberger, M. ; Matias-Garcia, P.R. ; Peters, A. ; Hodge, A.* ; Giles, G.G.* ; Schmitz, L.L.* ; Levine, M.* ; Smith, J.A.* ; Liu, Y.* ; Kee, F.* ; Young, I.S.* ; McGuinness, B.* ; McKnight, A.J.* ; van Meurs, J.* ; Voortman, T.* ; Kenny, R.A.* ; Vineis, P.* ; Carmeli, C.*

The role of epigenetic clocks in explaining educational inequalities in mortality: A multi-cohort study and meta-analysis.

J. Gerontol. A Biol. Sci. Med. Sci. 77, 1750-1759 (2022)
Postprint DOI PMC
Open Access Green
Educational inequalities in all-cause mortality have been observed for decades. However, the underlying biological mechanisms are not well known. We aimed to assess the role of DNA methylation changes in blood captured by epigenetic clocks in explaining these inequalities. Data were from eight prospective population-based cohort studies, representing 13,021 participants. First, educational inequalities and their portion explained by Horvath DNAmAge, Hannum DNAmAge, DNAmPhenoAge, and DNAmGrimAge epigenetic clocks were assessed in each cohort via counterfactual-based mediation models, on both absolute (hazard difference) and relative (hazard ratio) scales, and by sex. Second, estimates from each cohort were pooled through a random effect meta-analysis model. Men with low education had an excess mortality from all causes of 57 deaths per 10,000 person-years (95% confidence interval (CI): 38, 76) compared to their more advantaged counterparts. For women, the excess mortality was 4 deaths per 10,000 person-years (95% CI: -11, 19). On the relative scale, educational inequalities corresponded to hazard ratios of 1.33 (95% CI: 1.12, 1.57) for men and 1.15 (95% CI: 0.96, 1.37) for women. DNAmGrimAge accounted for the largest proportion, approximately 50%, of the educational inequalities for men, while the proportion was negligible for women. Most of this mediation was explained by differential effects of unhealthy lifestyles and morbidities of the WHO risk factors for premature mortality. These results support DNA methylation-based epigenetic aging as a signature of educational inequalities in life expectancy emphasizing the need for policies to address the unequal social distribution of these WHO risk factors.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Dna Methylation ; Biomarkers ; Longevity ; Social Inequalities
Sprache englisch
Veröffentlichungsjahr 2022
HGF-Berichtsjahr 2022
ISSN (print) / ISBN 1079-5006
e-ISSN 1758-535X
Zeitschrift Journals of Gerontology Series A: Biological Sciences and Medical Sciences
Quellenangaben Band: 77, Heft: 9, Seiten: 1750-1759 Artikelnummer: , Supplement: ,
Verlag Oxford University Press
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Health Economics and Health Care Management (IGM)
Institute of Epidemiology (EPI)
POF Topic(s) 30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-505300-001
G-504091-001
G-504000-010
Förderungen University of Sassari, Italy
European Commission
DOI 10.1093/gerona/glac041
WOS ID WOS:000830096400001
PubMed ID 35172329
Erfassungsdatum 2022-06-29
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