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Maternal smoking during gestation, differential DNA methylation, and changes in lung function at age 18 years

机译:妊娠期间的孕产妇吸烟,差异DNA甲基化和18岁时肺功能的变化

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Background: DNA methylation (DNA-M) is considered to constitute an archive of past exposures, which may link gestational exposures with child and adult health outcomes. Aims: In a birth cohort followed into early adulthood, we explored whether epigenome-wide DNA-M in peripheral blood cells is related to intra-uterine exposure to maternal smoking 18 years earlier and whether differentially methylated cytosine-phosphate-guanine dinucleotide (CpG) sites are associated with lung function in adolescence. Methods: Genome-wide DNA-M was assessed using the Illumina Infinium HumanMethylation450 BeadChip, which interrogates >484,000 CpG sites. We focused on DNA-M in 245 female participants at age 18, who were randomly selected from the total cohort. A training-testing procedure was used to optimize the identification of methylated CpG sites. Forced expiratory volume (FEV1), forced vital capacity (FVC), and the FEV1/FVC ratio were measured in children of the Isle of Wight birth cohort at age 18. Current smoking and cotinine urine levels were ascertained at age 18 years. Results: In utero cigarette smoke exposure was associated with statistically significant differential methylation, particularly of CpG sites of the cytochrome P450 aryl hydrocarbon hydroxylase (CYP1A1), aryl hydrocarbon receptor repressor (AHRR),contactin-associated protein-like 2 (CNTNAP2), and myosin 1G (MYO1G) genes. For instance, the methylation of the CpG site cg17924476 of the AHRR gene was increased in relation to gestational smoke exposure. In turn, controlling for height and active smoking, differential methylation of cg17924476 of the AHRR gene was associated with a statistically reduced FEV1/FVC ratio (range 62-100%). The FEV1/FVC ratio was diminished by 2% per increase of DNA-M of 10%. Conclusions: In utero smoke exposure seems to establish long-term memory via DNA methylation leading to a higher susceptibility for diminished lung function at age 18 years of age.
机译:背景:DNA甲基化(DNA-M)被认为构成过去曝光的档案,这可能将妊娠曝光与儿童和成人健康结果联系起来。目的:在成年早期的出生队列中,我们探讨了外周血细胞中外周血的DNA-M是否与早期的孕产妇吸烟有关,以及差异上甲基化胞嘧啶 - 磷酸胍 - 鸟嘌呤二核苷酸(CPG)是否有关。位点与青春期的肺功能相关。方法:使用Illumina Niminium人甲基化450珠芯片评估基因组DNA-M,其询问> 484,000个CPG位点。我们专注于245名女性参与者的DNA-M,于18岁时,从总队列中随机选择。用于优化甲基化CpG位点的鉴定的培训测试程序。强制呼气量(FEV1),强制生命能力(FVC),以及18岁的怀特生群岛儿童中测量了FEV1 / FVC比率。目前的吸烟和含有Cotinine尿液水平在18岁时确定。结果:在子宫卷烟烟雾中,与统计学显着的差异甲基化相关,特别是细胞色素P450芳基烃羟化酶(CYP1A1)的CPG位点,芳基烃受体抑制剂(AHRR),接触相关蛋白样2(CNTNAP2),以及肌球蛋白1g(myo1g)基因。例如,与妊娠烟雾暴露相比,AHRR基因的CPG位点CG17924476的甲基化增加。反过来,控制高度和活性吸烟,AHRR基因CG17924476的差异甲基化与统计学上减少的FEV1 / FVC比(范围62-100%)相关。每增加10%的DNA-M增加,FEV1 / FVC比率减少了2%。结论:在子宫烟雾曝光似乎通过DNA甲基化建立长期记忆,导致18岁的肺功能降低的易感性较高。

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