Institute for Health & Equity, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Epidemiology and Biostatistics, Dornsife School of Public Health, Drexel University, Philadelphia, PA, USA.
Soc Sci Med. 2023 Sep;333:116173. doi: 10.1016/j.socscimed.2023.116173. Epub 2023 Aug 12.
Epigenetic aging is one plausible mechanism by which socioeconomic status (SES) contributes to disparities in morbidity and mortality. Although the association between SES and epigenetic aging is well documented, the role of parental education into adulthood remains understudied. We examined (1) if parental education was independently associated with epigenetic aging, (2) whether upward educational mobility buffered this association, and (3) if the benefit of parental education was differentiated by race/ethnicity. Secondary data analysis of a subsample (n = 3875) of Non-Hispanic [NH] Black, Hispanic, NH White, and NH other race participants from the Venous Blood Study within Health and Retirement Study were examined. Thirteen clocks based on DNA methylation of cytosine-phosphate-guanine sites were used to calculate epigenetic aging. Participants' education (personal) and their report of their respective parent's education (parental; mother's and/or father's) were included as independent variables; several potential confounders were also included. Direct associations and interactions between parental and personal education were estimated via survey-weighted generalized linear models; marginal means for epigenetic aging were estimated and contrasts were made between the education subcategories. Analyses were also stratified by race/ethnicity. Our results showed that higher parental education was independently associated with slower epigenetic aging among four clocks, whereas higher personal education magnified this association among four different epigenetic clocks. Participants with the lowest parental and personal education had higher marginal means (i.e., accelerated aging) compared to participants with the highest parental and personal education, and there was little evidence of upward mobility. These associations were more frequently observed among NH White participants, whereas fewer were observed for Hispanic and NH Black participants. Overall, our findings support that early-life circumstances may be biologically embedded through epigenetic aging, which may also limit the biological benefits associated with one's own education.
表观遗传衰老可能是社会经济地位 (SES) 导致发病率和死亡率差异的一种机制。尽管 SES 与表观遗传衰老之间的关联已有充分记录,但父母教育对成年后的影响仍研究不足。我们研究了 (1) 父母教育是否与表观遗传衰老独立相关,(2) 教育向上流动是否缓冲了这种关联,以及 (3) 父母教育的益处是否因种族/民族而异。对健康与退休研究中的静脉血研究中的非西班牙裔黑人、西班牙裔、非西班牙裔白人以及其他种族参与者的子样本 (n=3875) 进行了二次数据分析。使用基于胞嘧啶-磷酸-鸟嘌呤位点 DNA 甲基化的 13 个时钟来计算表观遗传衰老。参与者的教育 (个人) 和他们各自父母的教育报告 (父母; 母亲和/或父亲) 被用作自变量; 还包括了几个潜在的混杂因素。通过调查加权广义线性模型估计了父母和个人教育之间的直接关联和相互作用; 估计了表观遗传衰老的边缘均值,并对教育亚类之间进行了对比。分析还按种族/民族进行了分层。我们的结果表明,较高的父母教育与四个时钟中的较慢的表观遗传衰老独立相关,而较高的个人教育则放大了这四个不同的表观遗传时钟中的关联。与具有最高父母和个人教育的参与者相比,具有最低父母和个人教育的参与者具有更高的边缘均值 (即加速衰老),而向上流动的证据很少。这些关联在非西班牙裔白人参与者中更为常见,而在西班牙裔和非西班牙裔黑人参与者中则较少。总体而言,我们的研究结果表明,早期生活环境可能通过表观遗传衰老在生物学上被嵌入,这也可能限制与自身教育相关的生物学益处。