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Prenatal exposure to drinking-water chlorination by-products cytochrome P450 gene polymorphisms and small-for-gestational-age neonates

机译:产前暴露于饮用水氯化副产物细胞色素P450基因多态性和小胎龄新生儿

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摘要

Genetic susceptibility may modulate chlorination by-products (CBPs) effects on fetal growth, especially genes coding for the cytochrome P450 involved in the metabolism of CBPs and steroidogenesis.In a case-control study of 1432 mother-child pairs, we assessed the association between maternal and child single nucleotide polymorphisms (SNPs) within CYP1A2, CYP2A6, CYP2D6 and CYP17A1 genes and small-for-gestational-age neonates (SGA <10th percentile) as well as interaction between these SNPs and maternal exposure to trihalomethanes or haloacetic acids (HAAs) during the third trimester of pregnancy.Interactions were found between mother and neonate carrying CYP17A1 rs4919687 A and rs743572 G alleles and maternal exposure to total trihalomethanes or five regulated HAAs species. However, these interactions became non statistically significant after correction for multiple testing.There is some evidence, albeit weak, of a potential effect modification of the association between CBPs and SGA by SNPs in CYP17A1 gene. Further studies are needed to validate these observations.
机译:遗传易感性可能会调节氯化副产物(CBP)对胎儿生长的影响,尤其是编码参与CBP代谢和类固醇生成的细胞色素P450的基因。在一项对1432对母子对的病例对照研究中,我们评估了两者之间的相关性CYP1A2,CYP2A6,CYP2D6和CYP17A1基因内的母婴单核苷酸多态性(SNP)和小胎龄新生儿(SGA <10 百分位数)以及这些SNP与母体之间的相互作用在妊娠晚期,CYP17A1 rs4919687 A和rs743572 G等位基因的母亲和新生儿之间发生了相互作用,母体暴露于总三卤甲烷或五种受管制的HAAs中。然而,经过多次测试校正后,这些相互作用变得无统计学意义。尽管有证据表明,CYP17A1基因中的SNP可能改变CBP与SGA之间的关联。需要进一步研究以验证这些观察结果。

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