Centre for Social Sciences, Athabasca University, Athabasca, AB, Canada.
Department of Psychiatry and Biobehavioral Sciences, Cousins Center for Psychoneuroimmunology, David Geffen School of Medicine, Semel Institute for Neuroscience and Human Behavior, University of California - Los Angeles, Los Angeles, CA, USA.
Am J Reprod Immunol. 2020 May;83(5):e13229. doi: 10.1111/aji.13229. Epub 2020 Mar 12.
Epigenetic age indices are markers of biological aging determined from DNA methylation patterns. Accelerated epigenetic age predicts morbidity and mortality. Women tend to demonstrate slower blood epigenetic aging compared to men, possibly due to female-specific hormones and reproductive milestones. Pregnancy and the post-partum period are critical reproductive periods that have not been studied yet with respect to epigenetic aging. The purpose of this paper was to examine whether pregnancy itself and an important pregnancy-related variable, changes in body mass index (BMI) between pregnancy and the post-partum period, are associated with epigenetic aging.
A pilot sample of 35 women was recruited as part of the Healthy Babies Before Birth (HB3) project. Whole blood samples were collected at mid-pregnancy and 1 year post-partum. DNA methylation at both time points was assayed using Infinium 450K and EPIC chips. Epigenetic age indices were calculated using an online calculator.
Paired-sample t-tests were used to test differences in epigenetic age indices from pregnancy to 1 year after birth. Over this critical time span, women became younger with respect to phenotypic epigenetic age, GrimAge, DNAm PAI-1, and epigenetic age indices linked to aging-related shifts in immune cell populations, known as extrinsic epigenetic age. Post-partum BMI retention, but not prenatal BMI increases, predicted accelerated epigenetic aging.
Women appear to become younger from pregnancy to the post-partum period based on specific epigenetic age indices. Further, BMI at 1 year after birth that reflects weight retention predicted greater epigenetic aging during this period.
表观遗传年龄指数是根据 DNA 甲基化模式确定的生物衰老标志物。加速的表观遗传年龄可预测发病率和死亡率。与男性相比,女性的血液表观遗传衰老速度较慢,这可能是由于女性特有的激素和生殖里程碑。妊娠和产后是关键的生殖期,但目前尚未研究它们与表观遗传衰老的关系。本文旨在探讨妊娠本身以及妊娠和产后期间体重指数 (BMI) 的变化是否与表观遗传衰老有关。
作为健康婴儿在出生前 (HB3) 项目的一部分,招募了 35 名女性的样本。在妊娠中期和产后 1 年采集全血样本。使用 Infinium 450K 和 EPIC 芯片检测两个时间点的 DNA 甲基化。使用在线计算器计算表观遗传年龄指数。
采用配对样本 t 检验测试从妊娠到产后 1 年表观遗传年龄指数的差异。在这个关键时间段内,女性在表型表观遗传年龄、GrimAge、DNAm PAI-1 和与免疫细胞群体衰老相关变化相关的表观遗传年龄指数方面变得更年轻,这些指数称为外在表观遗传年龄。产后 BMI 保留,但不是产前 BMI 增加,预测了加速的表观遗传衰老。
女性在妊娠到产后期间似乎根据特定的表观遗传年龄指数变得更年轻。此外,反映体重保留的产后 1 年 BMI 预测在此期间更大的表观遗传衰老。