Department of Epidemiology, Colorado School of Public Health, Aurora, Colorado, USA.
Lifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Environ Health Perspect. 2020 Dec;128(12):127014. doi: 10.1289/EHP6888. Epub 2020 Dec 24.
Per- and polyfluoroalkyl substances (PFAS) are environmentally persistent chemicals widely detected in women of reproductive age. Prenatal PFAS exposure is associated with adverse health outcomes in children. We hypothesized that DNA methylation changes may result from prenatal PFAS exposure and may be linked to offspring cardio-metabolic phenotype.
We estimated associations of prenatal PFAS with DNA methylation in umbilical cord blood. We evaluated associations of methylation at selected sites with neonatal cardio-metabolic indicators.
Among 583 mother-infant pairs in a prospective cohort, five PFAS were quantified in maternal serum (median 27 wk of gestation). Umbilical cord blood DNA methylation was evaluated using the Illumina HumanMethylation450 array. Differentially methylated positions (DMPs) were evaluated at a false discovery rate and differentially methylated regions (DMRs) were identified using comb-p (Šidák-adjusted ). We estimated associations between methylation at candidate DMPs and DMR sites and the following outcomes: newborn weight, adiposity, and cord blood glucose, insulin, lipids, and leptin.
Maternal serum PFAS concentrations were below the median for females in the U.S. general population. Moderate to high pairwise correlations were observed between PFAS concentrations (). Methylation at one DMP (cg18587484), annotated to the gene , was associated with perfluorooctanoate (PFOA) at . Comb-p detected between 4 and 15 DMRs for each PFAS. Associated genes, some common across multiple PFAS, were implicated in growth (), lipid homeostasis (, , , ), inflammation and immune activity (, ), among other functions. There was suggestive evidence that two PFAS-associated loci (cg09093485, cg09637273) were associated with cord blood triglycerides and birth weight, respectively ().
DNA methylation in umbilical cord blood was associated with maternal serum PFAS concentrations during pregnancy, suggesting potential associations with offspring growth, metabolism, and immune function. Future research should explore whether DNA methylation changes mediate associations between prenatal PFAS exposures and child health outcomes. https://doi.org/10.1289/EHP6888.
全氟和多氟烷基物质(PFAS)是广泛存在于育龄妇女中的环境持久性化学物质。产前 PFAS 暴露与儿童健康不良结局有关。我们假设 DNA 甲基化变化可能是由产前 PFAS 暴露引起的,并且可能与后代的心脏代谢表型有关。
我们估计了产前 PFAS 与脐带血 DNA 甲基化的关系。我们评估了选定部位的甲基化与新生儿心脏代谢指标的关系。
在一项前瞻性队列研究中,对 583 对母婴进行了研究,在妊娠 27 周时测量了母亲血清中的五种 PFAS(中位数)。使用 Illumina HumanMethylation450 阵列评估脐带血 DNA 甲基化。采用错误发现率(FDR)评估差异甲基化位置(DMP),并使用 comb-p(Šidák 调整)识别差异甲基化区域(DMR)。我们估计候选 DMP 和 DMR 位点的甲基化与以下结果之间的关系:新生儿体重、肥胖程度以及脐带血葡萄糖、胰岛素、脂质和瘦素。
母亲血清 PFAS 浓度低于美国一般女性人群的中位数。PFAS 浓度之间存在中度至高度的两两相关性()。一个 DMP(cg18587484)的甲基化与全氟辛烷磺酸(PFOA)相关()。comb-p 为每个 PFAS 检测到 4 到 15 个 DMR。相关基因在多个 PFAS 中是共同的,涉及生长()、脂质稳态(、、、)、炎症和免疫活性(、)等功能。有证据表明,两个与 PFAS 相关的基因座(cg09093485、cg09637273)分别与脐带血甘油三酯和出生体重相关()。
脐带血中的 DNA 甲基化与怀孕期间母亲血清中的 PFAS 浓度相关,表明与后代的生长、代谢和免疫功能有关。未来的研究应该探讨 DNA 甲基化变化是否介导了产前 PFAS 暴露与儿童健康结果之间的关系。