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Polychlorinated biphenyl exposure and DNA methylation in the Anniston Community Health Survey

机译:亚纳斯顿社区健康调查中的多氯联苯暴露和DNA甲基化

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摘要

Anniston, Alabama was home to a major polychlorinated biphenyl (PCB) production facility from 1929 until 1971. The Anniston Community Health Survey I and II (ACHS-I 2005–2007, ACHS-II 2013–2014) were conducted to explore the effects of PCB exposures. In this report we examined associations between PCB exposure and DNA methylation in whole blood using EPIC arrays (ACHS-I, n = 518; ACHS-II, n = 299). For both cohorts, 35 PCBs were measured in serum. We modelled methylation versus PCB wet-weight concentrations for: the sum of 35 PCBs, mono-ortho substituted PCBs, di-ortho substituted PCBs, tri/tetra-ortho substituted PCBs, oestrogenic PCBs, and antiestrogenic PCBs. Using robust multivariable linear regression, we adjusted for age, race, sex, smoking, total lipids, and six blood cell-type percentages. We carried out a two-stage analysis; discovery in ACHS-I followed by replication in ACHS-II. In ACHS-I, we identified 28 associations (17 unique CpGs) at p ≤ 6.70E-08 and 369 associations (286 unique CpGs) at FDR p ≤ 5.00E-02. A large proportion of the genes have been observed to interact with PCBs or dioxins in model studies. Among the 28 genome-wide significant CpG/PCB associations, 14 displayed replicated directional effects in ACHS-II; however, only one in ACHS-II was statistically significant at p ≤ 1.70E-04. While we identified many novel CpGs significantly associated with PCB exposures in ACHS-I, the differential methylation was modest and the effect was attenuated seven years later in ACHS-II, suggesting a lack of persistence of the associations between PCB exposures and altered DNA methylation in blood cells.
机译:Anniston,Alabama是从1929年的主要多氯联苯(PCB)生产设施的所在地,直到1971年。纳尼昂社区卫生调查I和II(ACHS-I 2005-2007,ACHS-II 2013-2014)进行了探索PCB曝光。在本报告中,我们使用史诗阵列(ACHS-I,N = 518; ACH-II,N = 299)检查全血PCB暴露和DNA甲基化之间的关联。对于两个群组,在血清中测量35个键。我们建模甲基化与PCB湿重浓度为:35个多氯联苯,单邻取代的PCB,二邻取代的PCB,三/四邻醇取代的PCB,即雌激素PCB和抗雌激素PCB。我们使用稳健的多变量线性回归,我们调整年龄,种族,性别,吸烟,全脂脂质和六种血细胞型百分比。我们进行了两阶段的分析;在ACHS中发现 - 我在ACHS-II中进行复制。在ACHS-I中,我们在FDRP≤5.00E-02处识别了P≤6.70E-08和369关联(286个独特CPG)的28个关联(17个唯一CPG)。已经观察到大部分基因与模型研究中的PCB或二恶英相互作用。在28个基因组 - 范围的显着CpG / PCB关联中,14个在ACHS-II中显示出复制的定向效果;然而,ACHS-II中只有一个在p≤1.70e-04时具有统计学意义。虽然我们识别出与ACH-I中的PCB曝光明显相关的新型CPG,但差异甲基化是适度的,并且在ACHS-II中七年后效果衰减,表明PCB暴露之间的关联持续存在,并改变了DNA甲基化的关联持续存在。血细胞。

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