Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA.
Epigenetics. 2013 Jan;8(1):23-7. doi: 10.4161/epi.22989. Epub 2012 Nov 29.
Epigenetic modifications may be one mechanism linking early life factors, including parental socioeconomic status (SES), to adult onset disease risk. However, SES influences on DNA methylation patterns remain largely unknown. In a US birth cohort of women, we examined whether indicators of early life and adult SES were associated with white blood cell methylation of repetitive elements (Sat2, Alu and LINE-1) in adulthood. Low family income at birth was associated with higher Sat2 methylation (β = 19.7, 95% CI: 0.4, 39.0 for lowest vs. highest income quartile) and single parent family was associated with higher Alu methylation (β = 23.5, 95% CI: 2.6, 44.4), after adjusting for other early life factors. Lower adult education was associated with lower Sat2 methylation (β = -16.7, 95% CI: -29.0, -4.5). There were no associations between early life SES and LINE-1 methylation. Overall, our preliminary results suggest possible influences of SES across the life-course on genomic DNA methylation in adult women. However, these preliminary associations need to be replicated in larger prospective studies.
表观遗传修饰可能是将包括父母社会经济地位(SES)在内的早期生活因素与成年发病风险联系起来的一种机制。然而,SES 对 DNA 甲基化模式的影响在很大程度上仍不清楚。在一项美国出生队列的女性研究中,我们研究了早期生活和成年 SES 指标是否与成年时白细胞中重复元件(Sat2、Alu 和 LINE-1)的甲基化有关。出生时家庭收入较低与 Sat2 甲基化水平较高相关(β=19.7,95%CI:0.4,39.0,最低与最高四分位数比较),单亲家庭与 Alu 甲基化水平较高相关(β=23.5,95%CI:2.6,44.4),在调整了其他早期生活因素后。成人教育程度较低与 Sat2 甲基化水平较低相关(β=-16.7,95%CI:-29.0,-4.5)。早期 SES 与 LINE-1 甲基化之间没有关联。总体而言,我们的初步结果表明,SES 可能会在整个生命过程中对成年女性的基因组 DNA 甲基化产生影响。然而,这些初步关联需要在更大的前瞻性研究中进行复制。