Accelerated biological aging six decades after prenatal famine exposure

Author:

Cheng Mengling12ORCID,Conley Dalton3ORCID,Kuipers Tom4,Li Chihua56ORCID,Ryan Calen P.2ORCID,Taeubert M. Jazmin4ORCID,Wang Shuang7,Wang Tian7,Zhou Jiayi2,Schmitz Lauren L.8ORCID,Tobi Elmar W.4ORCID,Heijmans Bastiaan T.4,Lumey L. H.46ORCID,Belsky Daniel W.26ORCID

Affiliation:

1. Swiss Centre of Expertise in Life Course Research, Faculty of Social and Political Sciences, University of Lausanne, Lausanne CH 1015, Switzerland

2. Robert N. Butler Columbia Aging Center, Mailman School of Public Health, Columbia University, New York, NY 10032

3. Department of Sociology, Princeton University, Mercer, NJ 08544

4. Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden ZC 2333, Netherlands

5. Institute for Social Research, University of Michigan at Ann Arbor, Ann Arbor, MI 48106

6. Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY 10032

7. Department of Biostatistics, Columbia University Mailman School of Public Health, New York, NY 10032

8. Center for Demography and Ecology, Robert M. La Follette School of Public Affairs, University of Wisconsin-Madison, Madison, WI 53706

Abstract

To test the hypothesis that early-life adversity accelerates the pace of biological aging, we analyzed data from the Dutch Hunger Winter Families Study (DHWFS, N = 951). DHWFS is a natural-experiment birth-cohort study of survivors of in-utero exposure to famine conditions caused by the German occupation of the Western Netherlands in Winter 1944 to 1945, matched controls, and their siblings. We conducted DNA methylation analysis of blood samples collected when the survivors were aged 58 to quantify biological aging using the DunedinPACE, GrimAge, and PhenoAge epigenetic clocks. Famine survivors had faster DunedinPACE, as compared with controls. This effect was strongest among women. Results were similar for GrimAge, although effect-sizes were smaller. We observed no differences in PhenoAge between survivors and controls. Famine effects were not accounted for by blood-cell composition and were similar for individuals exposed early and later in gestation. Findings suggest in-utero undernutrition may accelerate biological aging in later life.

Funder

HHS | NIH | National Institute on Aging

Canadian Institute for Advanced Research Child Brain Development Network

NIDI/NIAS/UMCG Fellowship, Royal Netherlands Academy of Sciences KNAW at the Netherlands Institute for Advanced Study

Swiss National Science Foundation

Marie Sklodowska-Curie Grant

Netherlands Organization for Scientific Research

ZonMw

Publisher

Proceedings of the National Academy of Sciences

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