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首页> 外文期刊>Journal of developmental origins of health and disease >Association of in vitro fertilization with global and IGF2/H19 methylation variation in newborn twins
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Association of in vitro fertilization with global and IGF2/H19 methylation variation in newborn twins

机译:新生儿双胞胎体外受精与整体和IGF2 / H19甲基化变异的关系

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摘要

In vitro fertilization (IVF) and its subset intracytoplasmic sperm injection (ICSI), are widely used medical treatments for conception. There has been controversy over whether IVF is associated with adverse short- and long-term health outcomes of offspring. As with other prenatal factors, epigenetic change is thought to be a molecular mediator of any in utero programming effects. Most studies focused on DNA methylation at gene-specific and genomic level, with only a few on associations between DNA methylation and IVF. Using buccal epithelium from 208 twin pairs from the Peri/Postnatal Epigenetic Twin Study (PETS), we investigated associations between IVF and DNA methylation on a global level, using the proxies of Alu and LINE-1 interspersed repeats in addition to two locus-specific regulatory regions within IGF2/H19, controlling for 13 potentially confounding factors. Using multiple correction testing, we found strong evidence that IVF-conceived twins have lower DNA methylation in Alu, and weak evidence of lower methylation in one of the two IGF2/H19 regulatory regions and LINE-1, compared with naturally conceived twins. Weak evidence of a relationship between ICSI and DNA methylation within IGF2/H19 regulatory region was found, suggesting that one or more of the processes associated with IVF/ICSI may contribute to these methylation differences. Lower within- and between-pair DNA methylation variation was also found in IVF-conceived twins for LINE-1, Alu and one IGF2/H19 regulatory region. Although larger sample sizes are needed, our results provide additional insight to the possible influence of IVF and ICSI on DNA methylation. To our knowledge, this is the largest study to date investigating the association of IVF and DNA methylation.
机译:体外受精(IVF)及其子集的胞浆内精子注射(ICSI)是广泛用于受孕的药物。关于IVF是否与后代短期和长期健康不良后果相关,一直存在争议。与其他产前因素一样,表观遗传学改变被认为是子宫内任何编程作用的分子介体。大多数研究集中在基因特异性和基因组水平的DNA甲基化,只有少数研究涉及DNA甲基化和IVF之间的关联。使用来自围产期/产后表观遗传学双胎研究(PETS)的208对双胞胎的颊上皮,我们在全球范围内研究了IVF和DNA甲基化之间的关联,除了两个基因座特异性外,还使用了Alu和LINE-1散布的重复序列IGF2 / H19内的调控区,控制13个潜在的混杂因素。通过多次校正测试,我们发现有力的证据表明,与自然受孕的双胞胎相比,IVF受孕的双胞胎在Alu中的DNA甲基化程度较低,而在两个IGF2 / H19调节区和LINE-1中的甲基化程度较低的证据较弱。在IGF2 / H19调控区域内,ICSI和DNA甲基化之间关系的证据很弱,这表明与IVF / ICSI相关的一种或多种过程可能会导致这些甲基化差异。在IVF设想的双胞胎中,LINE-1,Alu和一个IGF2 / H19调控区的配对内和配对间DNA甲基化变异也较低。尽管需要更大的样本量,但我们的结果为IVF和ICSI对DNA甲基化的可能影响提供了更多见解。据我们所知,这是迄今最大的研究,试管婴儿和DNA甲基化的关联。

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