1Istituto Auxologico Italiano IRCCS, 20095 Cusano Milanino, Italy.
5Department of Brain and Behavioral Sciences, University of Pavia, 27100 Pavia, Italy.
Clin Epigenetics. 2018 Jun 8;10:77. doi: 10.1186/s13148-018-0510-3. eCollection 2018.
An increased incidence of imprint-associated disorders has been reported in babies born from assisted reproductive technology (ART). However, previous studies supporting an association between ART and an altered DNA methylation status of the conceived babies have been often conducted on a limited number of methylation sites and without correction for critical potential confounders. Moreover, all the previous studies focused on the identification of methylation changes shared among subjects while an evaluation of stochastic differences has never been conducted. This study aims to evaluate the effect of ART and other common behavioral or environmental factors associated with pregnancy on stochastic epigenetic variability using a multivariate approach.
DNA methylation levels of cord blood from 23 in vitro and 41 naturally conceived children were analyzed using the Infinium HumanMethylation450 BeadChips. After multiple testing correction, no statistically significant difference emerged in the number of cord blood stochastic epigenetic variations or in the methylation levels between in vitro- and in vivo-conceived babies. Conversely, four multiple factor analysis dimensions summarizing common phenotypic, behavioral, or environmental factors (cord blood cell composition, pre or post conception supplementation of folates, birth percentiles, gestational age, cesarean section, pre-gestational mother's weight, parents' BMI and obesity status, presence of adverse pregnancy outcomes, mother's smoking status, and season of birth) were significantly associated with stochastic epigenetic variability. The stochastic epigenetic variation analysis allowed the identification of a rare imprinting defect in the locus GNAS in one of the babies belonging to the control population, which would not have emerged using a classical case-control association analysis.
We confirmed the effect of several common behavioral or environmental factors on the epigenome of newborns and described for the first time an epigenetic effect related to season of birth. Children born after ART did not appear to have an increased risk of genome-wide changes in DNA methylation either at specific loci or randomly scattered throughout the genome. The inability to identify differences between cases and controls suggests that the number of stochastic epigenetic variations potentially induced by ART was not greater than that naturally produced in response to maternal behavior or other common environmental factors.
辅助生殖技术(ART)出生的婴儿中,印记相关疾病的发病率有所增加。然而,先前支持 ART 与所受孕婴儿的 DNA 甲基化状态改变之间存在关联的研究,通常是在有限数量的甲基化位点上进行的,并且没有对关键潜在混杂因素进行校正。此外,所有先前的研究都集中在识别受试者之间共享的甲基化变化上,而从未进行过随机差异的评估。本研究旨在使用多变量方法评估 ART 和其他与妊娠相关的常见行为或环境因素对随机表观遗传变异性的影响。
使用 Infinium HumanMethylation450 BeadChips 分析了 23 名体外受精和 41 名自然受孕婴儿的脐带血 DNA 甲基化水平。经过多次测试校正,体外受精和体内受精婴儿的脐带血随机表观遗传变异数量或甲基化水平没有统计学上的显著差异。相反,四个多因素分析维度概括了常见的表型、行为或环境因素(脐带血细胞组成、受孕前或受孕后叶酸补充、出生百分位数、胎龄、剖宫产、受孕前母亲体重、父母 BMI 和肥胖状况、不良妊娠结局的存在、母亲吸烟状况和出生季节)与随机表观遗传变异性显著相关。随机表观遗传变异分析允许在对照组的一个婴儿中鉴定出位于 GNAS 基因座的罕见印迹缺陷,而使用经典的病例对照关联分析则无法发现该缺陷。
我们证实了几个常见的行为或环境因素对新生儿表观基因组的影响,并首次描述了与出生季节相关的表观遗传效应。出生于 ART 后的儿童似乎没有增加在特定基因座或整个基因组中随机散布的 DNA 甲基化全基因组改变的风险。无法在病例和对照组之间识别差异表明,ART 潜在诱导的随机表观遗传变异数量并不大于母体行为或其他常见环境因素自然产生的数量。