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In Utero Exposure to Diethylstilbestrol and Blood DNA Methylation in Women Ages 40–59 Years from the Sister Study

机译:姊妹研究显示子宫暴露于己烯雌酚和血液DNA甲基化的年龄在40-59岁之间

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摘要

In utero exposure to diethylstilbestrol (DES) has been associated with increased risk of adverse health outcomes such as fertility problems and vaginal as well as breast cancer. Animal studies have linked prenatal DES exposure to lasting DNA methylation changes. We investigated genome-wide DNA methylation and in utero DES exposure in a sample of non-Hispanic white women aged 40–59 years from the Sister Study, a large United States cohort study of women with a family history of breast cancer. Using questionnaire information from women and their mothers, we selected 100 women whose mothers reported taking DES while pregnant and 100 control women whose mothers had not taken DES. DNA methylation in blood was measured at 485,577 CpG sites using the Illumina HumanMethylation450 BeadChip. Associations between CpG methylation and DES exposure status were analyzed using robust linear regression with adjustment for blood cell composition and multiple comparisons. Although four CpGs had p<105, after accounting for multiple comparisons using the false discovery rate (FDR), none reached genome-wide significance. In conclusion, adult women exposed to DES in utero had no evidence of large persistent changes in blood DNA methylation.
机译:子宫内暴露于己烯雌酚(DES)与不良健康后果(例如生育问题,阴道以及乳腺癌)的风险增加相关。动物研究已将产前DES暴露与持久的DNA甲基化变化联系起来。我们调查了Sister研究中40-59岁的非西班牙裔白人女性样本中的全基因组DNA甲基化和子宫内DES暴露,该研究是一项针对美国有乳腺癌家族史的女性的大型队列研究。利用来自妇女及其母亲的问卷调查信息,我们选择了100名母亲在怀孕时服用DES的妇女和100名母亲未服用DES的对照妇女。使用Illumina HumanMethylation450 BeadChip在485,577 CpG位点测量了血液中的DNA甲基化。 CpG甲基化与DES暴露状态之间的关联使用稳健的线性回归分析,并调整了血细胞组成并进行了多次比较。尽管四个CpG具有p <10 5 ,但在使用错误发现率(FDR)进行多次比较后,没有一个达到全基因组意义。总之,在子宫内暴露于DES的成年女性没有证据表明血液DNA甲基化有较大的持续变化。

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