School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
CANSEARCH Research Laboratory, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Environ Int. 2020 Dec;145:106148. doi: 10.1016/j.envint.2020.106148. Epub 2020 Sep 30.
Perfluoroalkyl substances (PFAS) are widespread synthetic substances with various adverse health effects. A potential mechanism of toxicity for PFAS is via epigenetic changes, such as DNA methylation. However, few studies have evaluated associations between PFAS exposure and DNA methylation among adults, and data is especially scarce for women. Furthermore, exposure to environmental pollutants has been associated with epigenetic age acceleration, but no studies have yet evaluated whether PFAS is associated with epigenetic age acceleration.
To investigate whether exposure to PFAS is associated with alteration of DNA methylation and epigenetic age acceleration among women.
In this observational pilot study, 59 women (aged 20-47 years at enrollment in 2014) from Ronneby, Sweden, an area with historically high PFAS exposure due to local drinking water contamination, were divided into three PFAS exposure groups (low, medium, and high). Genome-wide methylation of whole-blood DNA was analyzed using the Infinium MethylationEPIC BeadChip. Ingenuity Pathway Analysis was used for in silico functional assessment. Epigenetic age acceleration was derived from the DNA methylation data using Horvath's epigenetic skin and blood clock.
117 differentially methylated positions (q < 0.017) and one near-significantly differentially methylated region (S100A13, FWER = 0.020) were identified. In silico functional analyses suggested that genes with altered DNA methylation (q < 0.05) were annotated to cancer, endocrine system disorders, reproductive system disease, as well as pathways such as estrogen receptor signaling, cardiac hypertrophy signaling, PPARα/RXRα activation and telomerase signaling. No differences in epigenetic age acceleration between PFAS exposure groups were noted (p = 0.43).
The data suggests that PFAS exposure alters DNA methylation in women highly exposed to PFAS from drinking water. The observed associations should be verified in larger cohorts, and it should also be further investigated whether these changes in methylation also underlie potential phenotypic changes and/or adverse health effects of PFAS.
全氟烷基物质(PFAS)是广泛存在的合成物质,具有多种不良健康影响。PFAS 的潜在毒性机制是通过表观遗传变化,如 DNA 甲基化。然而,很少有研究评估 PFAS 暴露与成年人的 DNA 甲基化之间的关联,而且女性的数据尤其稀缺。此外,环境污染物的暴露与表观遗传年龄加速有关,但尚无研究评估 PFAS 是否与表观遗传年龄加速有关。
研究 PFAS 暴露是否与女性的 DNA 甲基化改变和表观遗传年龄加速有关。
在这项观察性的初步研究中,我们招募了来自瑞典罗恩比的 59 名女性(入组时年龄为 20-47 岁,2014 年),该地区由于当地饮用水污染,历史上 PFAS 暴露水平较高。这些女性被分为三组 PFAS 暴露组(低、中、高)。使用 Infinium MethylationEPIC BeadChip 分析全血 DNA 的全基因组甲基化。使用 Ingenuity Pathway Analysis 进行计算机功能评估。使用 Horvath 的表观遗传皮肤和血液时钟从 DNA 甲基化数据中推导表观遗传年龄加速。
发现了 117 个差异甲基化位置(q < 0.017)和一个接近显著差异甲基化区域(S100A13,FWER = 0.020)。计算机功能分析表明,改变 DNA 甲基化的基因(q < 0.05)被注释为癌症、内分泌系统紊乱、生殖系统疾病以及雌激素受体信号、心脏肥大信号、PPARα/RXRα 激活和端粒酶信号等途径。PFAS 暴露组之间的表观遗传年龄加速没有差异(p = 0.43)。
数据表明,PFAS 暴露会改变饮用水中 PFAS 高度暴露的女性的 DNA 甲基化。这些关联应该在更大的队列中进行验证,还应该进一步研究这些甲基化变化是否也构成了 PFAS 的潜在表型变化和/或不良健康影响的基础。