4.6 Article

The Early Life Course of Body Weight and Gene Expression Signatures for Disease

期刊

AMERICAN JOURNAL OF EPIDEMIOLOGY
卷 190, 期 8, 页码 1533-1540

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/aje/kwab049

关键词

birth weight; cardiovascular disease; gene expression; inflammation; life course; obesity; type 2 diabetes

资金

  1. National Institutes of Health [R01-HD087061, P30AG017265, R01-AG043404, R01-AG033590]
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development [P01-HD31921]
  3. Jacobs Center for Productive Youth Development, University of Zurich

向作者/读者索取更多资源

The study found that body weight is associated with gene expression signatures of cardiovascular disease and type 2 diabetes in sensitive periods, with birth weight having a significant impact on these features, while recent adult obesity status is also important. The association between body size and inflammation aligns with the accumulation model.
We examined the way body-weight patterns through the first 4 decades of life relate to gene expression signatures of common forms of morbidity, including cardiovascular disease (CVD), type 2 diabetes (T2D), and inflammation. As part of wave V of the nationally representative National Longitudinal Study of Adolescent to Adult Health (1997-2018) in the United States, mRNA abundance data were collected from peripheral blood (n = 1,132). We used a Bayesian modeling strategy to examine the relative associations between body size at 5 life stages-birth, adolescence, early adulthood, young adulthood, and adulthood-and gene expression-based disease signatures. We compared life-course models that consider critical or sensitive periods, as well as accumulation over the entire period. Our results are consistent with a sensitive-period model when examining CVD and T2D gene expression signatures: Birth weight has a prominent role for the CVD and T2D signatures (explaining 33.1% and 22.1%, respectively, of the total association accounted for by body size), while the most recent adult obesity status (ages 33-39) is important for both of these gene expression signatures (24.3% and 35.1%, respectively). Body size in all life stages was associated with inflammation, consistent with the accumulation model.

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