Janssen Bram G, Gyselaers Wilfried, Byun Hyang-Min, Roels Harry A, Cuypers Ann, Baccarelli Andrea A, Nawrot Tim S
Centre for Environmental Sciences, Hasselt University, Hasselt, Belgium.
Department of Obstetrics, East-Limburg Hospital, Genk, Belgium.
J Transl Med. 2017 Jan 4;15(1):5. doi: 10.1186/s12967-016-1113-4.
Maternal smoking during pregnancy results in an increased risk of low birth weight through perturbations in the utero-placental exchange. Epigenetics and mitochondrial function in fetal tissues might be molecular signatures responsive to in utero tobacco smoke exposure.
In the framework of the ENVIRONAGE birth cohort, we investigated the effect of self-reported tobacco smoke exposure during pregnancy on birth weight and the relation with placental tissue markers such as, (1) relative mitochondrial DNA (mtDNA) content as determined by real-time quantitative PCR, (2) DNA methylation of specific loci of mtDNA (D-loop and MT-RNR1), and (3) DNA methylation of the biotransformation gene CYP1A1 (the last two determined by bisulfite-pyrosequencing). The total pregnant mother sample included 255 non-smokers, 65 former-smokers who had quit smoking before pregnancy, and 62 smokers who continued smoking during pregnancy.
Smokers delivered newborns with a birth weight on average 208 g lower [95% confidence interval (CI) -318 to -99, p = 0.0002] than mothers who did not smoke during pregnancy. In the smoker group, the relative mtDNA content was lower (-21.6%, 95% CI -35.4 to -4.9%, p = 0.01) than in the non-smoker group; whereas, absolute mtDNA methylation levels of MT-RNR1 were higher (+0.62%, 95% CI 0.21 to 1.02%, p = 0.003). Lower CpG-specific methylation of CYP1A1 in placental tissue (-4.57%, 95% CI -7.15 to -1.98%, p < 0.0001) were observed in smokers compared with non-smokers. Nevertheless, no mediation of CYP1A1 methylation nor any other investigated molecular signature was observed for the association between tobacco smoke exposure and birth weight.
mtDNA content, methylation of specific loci of mtDNA, and CYP1A1 methylation in placental tissue may serve as molecular signatures for the association between gestational tobacco smoke exposure and low birth weight.
孕期母亲吸烟会通过干扰子宫 - 胎盘交换增加低出生体重的风险。胎儿组织中的表观遗传学和线粒体功能可能是对子宫内烟草烟雾暴露有反应的分子特征。
在ENVIRONAGE出生队列研究框架内,我们调查了孕期自我报告的烟草烟雾暴露对出生体重的影响以及与胎盘组织标志物的关系,这些标志物包括:(1)通过实时定量PCR测定的相对线粒体DNA(mtDNA)含量;(2)mtDNA特定基因座(D - 环和MT - RNR1)的DNA甲基化;(3)生物转化基因CYP1A1的DNA甲基化(后两者通过亚硫酸氢盐焦磷酸测序测定)。总共有255名非吸烟孕妇、65名在怀孕前戒烟的曾经吸烟者以及62名孕期继续吸烟的吸烟者纳入了孕妇样本。
吸烟者所生新生儿的出生体重平均比孕期不吸烟的母亲所生新生儿低208克[95%置信区间(CI)-318至-99,p = 0.0002]。在吸烟者组中,相对mtDNA含量低于非吸烟者组(-21.6%,95% CI -35.4至-4.9%,p = 0.01);而MT - RNR1的绝对mtDNA甲基化水平更高(+0.62%,95% CI 0.21至1.02%,p = 0.003)。与非吸烟者相比,吸烟者胎盘组织中CYP1A1的CpG特异性甲基化水平更低(-4.57%,95% CI -7.15至-1.98%,p < 0.0001)。然而,未观察到CYP1A1甲基化或任何其他研究的分子特征在烟草烟雾暴露与出生体重之间的关联中起中介作用。
胎盘组织中的mtDNA含量、mtDNA特定基因座的甲基化以及CYP1A1甲基化可能作为孕期烟草烟雾暴露与低出生体重之间关联的分子特征。