Pregnancy is linked to faster epigenetic aging in young women

• 成果类型: Article
• 署名作者: Ryan, Calen P.; Lee, Nanette R.; Carba, Delia B.; Macisaac, Julie L.; Lin, David T. S.; Atashzay, Parmida; Belsky, Daniel W.; Kobor, Michael S.; Kuzawa, Christopher W.
• 署名单位: Columbia University; University of San Carlos; BC Children's Hospital; BC Children's Hospital Research Institute; University of British Columbia; Columbia University; Canadian Institute for Advanced Research (CIFAR); University of British Columbia; Northwestern University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-11634
• DOI: 10.1073/pnas.2317290121
• 发表日期: 2024-04-16
• 关键词: cebu longitudinal health; genome-wide association; c-reactive protein; trade-offs; later life; mortality; HISTORY; COSTS; reproduction; fertility

摘要

A central prediction of evolutionary theory is that energy invested into reproduction comes at the expense of somatic maintenance and repair, accelerating biological aging. Supporting this prediction are findings that high fertility among women predicts shorter lifespan and poorer health later in life. However, biological aging is thought to begin before age- related health declines, limiting the applicability of morbidity and mortality for studying the aging process earlier in life. Here, we examine the relationship between reproductive history and biological aging in a sample of young (20 to 22yo) men and women from the Cebu Longitudinal Health and Nutrition Survey, located in the Philippines (n = 1,735). We quantify biological aging using six measures, collectively known as epigenetic clocks, reflecting various facets of cellular aging, health, and mortality risk. In a subset of women, we test whether longitudinal changes in gravidity between young and early-middle adulthood (25 to 31yo) are associated with changes in epigenetic aging during that time. Cross- sectionally, gravidity was associated with all six measures of accelerated epigenetic aging in women (n = 825). Furthermore, longitudinal increases in gravidity were linked to accelerated epigenetic aging in two epigenetic clocks (n = 331). In contrast, the number of pregnancies a man reported fathering was not associated with epigenetic aging among same-aged cohort men (n = 910). These effects were robust to socioecological, environmental, and immunological factors, consistent with the hypothesis that pregnancy accelerates biological aging and that these effects can be detected in young women in a high- fertility context.