Department of Environmental Health Sciences, School of Public Health, University of Michigan, 1415 Washington Heights, Ann Arbor, MI, 48109, USA.
Epigenomics Core, Biomedical Research Core Facilities, University of Michigan Medical School, Ann Arbor, MI, USA.
Clin Epigenetics. 2023 Mar 24;15(1):49. doi: 10.1186/s13148-023-01461-5.
Per- and polyfluoroalkyl substances (PFAS) are chemicals that are resistant to degradation and ubiquitous in our environments. PFAS may impact the developing epigenome, but current human evidence is limited to assessments of total DNA methylation. We assessed associations between first trimester PFAS exposures with newborn DNA methylation, including 5-methylcytosine (5-mC) and 5-hydroxymethylcytosine (5-hmC). DNA methylation mediation of associations between PFAS and birth outcomes were explored in the Michigan Mother Infant Pairs cohort. Nine PFAS were measured in maternal first trimester blood. Seven were highly detected and included for analysis: PFHxS, PFOA, PFOS, PFNA, PFDA, PFUnDA, and MeFOSAA. Bisulfite-converted cord blood DNA (n = 141) and oxidative-bisulfite-converted cord blood (n = 70) were assayed on Illumina MethylationEPIC BeadChips to measure total DNA methylation (5-mC + 5-hmC) and 5-mC/5-hmC. Correcting for multiple comparisons, beta regressions were used to assess associations between levels of PFAS and total methylation, 5-mC, or 5-hmC. Nonlinear mediation analyses were used to assess the epigenetic meditation effect between PFAS and birth outcomes.
PFAS was significantly associated with total methylation (q < 0.05: PFHxS-12 sites; PFOS-19 sites; PFOA-2 sites; PFNA-3 sites; PFDA-4 sites). In 72 female infants and 69 male infants, there were sex-specific associations between five PFAS and DNA methylation. 5-mC and 5-hmC were each significantly associated with thousands of sites for PFHxS, PFOS, PFNA, PFDA, PFUnDA, and MeFOSAA (q < 0.05). Clusters of 5-mC and 5-hmC sites were significant mediators between PFNA and PFUnDA and decreased gestational age (q < 0.05).
This study demonstrates the mediation role of specific types of DNA methylation on the relationship between PFAS exposure and birth outcomes. These results suggest that 5-mC and 5-hmC may be more sensitive to the developmental impacts of PFAS than total DNA methylation.
全氟和多氟烷基物质(PFAS)是抗降解且在环境中普遍存在的化学物质。PFAS 可能会影响发育中的表观基因组,但目前人类的证据仅限于对总 DNA 甲基化的评估。我们评估了妊娠早期 PFAS 暴露与新生儿 DNA 甲基化之间的关联,包括 5-甲基胞嘧啶(5-mC)和 5-羟甲基胞嘧啶(5-hmC)。在密歇根母婴对子队列中,我们探索了 PFAS 与出生结局之间关联的 DNA 甲基化中介作用。在母亲妊娠早期的血液中测量了 9 种 PFAS。其中 7 种高度检出并纳入分析:PFHxS、PFOA、PFOS、PFNA、PFDA、PFUnDA 和 MeFOSAA。对 141 例脐带血 DNA 进行亚硫酸氢盐转化,对 70 例脐带血进行氧化亚硫酸氢盐转化,然后用 Illumina MethylationEPIC BeadChips 检测总 DNA 甲基化(5-mC+5-hmC)和 5-mC/5-hmC。在进行多重比较校正后,使用贝叶斯回归评估 PFAS 水平与总甲基化、5-mC 或 5-hmC 之间的关联。使用非线性中介分析评估 PFAS 与出生结局之间的表观遗传中介效应。
PFAS 与总甲基化显著相关(q<0.05:PFHxS-12 个位点;PFOS-19 个位点;PFOA-2 个位点;PFNA-3 个位点;PFDA-4 个位点)。在 72 名女性婴儿和 69 名男性婴儿中,有五个 PFAS 与 DNA 甲基化之间存在性别特异性关联。PFHxS、PFOS、PFNA、PFDA、PFUnDA 和 MeFOSAA 的每个都与数千个 5-mC 和 5-hmC 位点显著相关(q<0.05)。PFNA 和 PFUnDA 与胎龄降低之间的 5-mC 和 5-hmC 位点簇是显著的中介(q<0.05)。
本研究证明了特定类型的 DNA 甲基化在 PFAS 暴露与出生结局之间关系中的中介作用。这些结果表明,5-mC 和 5-hmC 可能比总 DNA 甲基化对 PFAS 的发育影响更敏感。