双酚A (BPA)和邻苯二甲酸盐暴露对人类胎盘表观遗传结果的影响。

IF 4.8 Q1 GENETICS & HEREDITY
Environmental Epigenetics Pub Date : 2018-09-07 eCollection Date: 2018-07-01 DOI:10.1093/eep/dvy022
Rita S Strakovsky, Susan L Schantz
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引用次数: 61

摘要

胎盘引导胎儿生长发育。双酚A (BPA)和邻苯二甲酸盐是广泛存在的环境污染物和内分泌干扰物,胎盘对这些化学物质的表观遗传反应是一个日益增长的研究兴趣领域。因此,我们的目标是总结BPA或邻苯二甲酸盐暴露与人类妊娠胎盘结局之间的联系,特别关注表观遗传终点。在PubMed中,如果研究报告了双酚a或邻苯二甲酸盐对人类胎盘的任何直接影响,则选择研究进行审查(不限制开始日期,截止日期为2018年5月1日)。总的来说,现有的研究表明BPA和邻苯二甲酸盐暴露与胎盘微rna表达、DNA甲基化和基因组印记的变化有关。此外,一些研究表明胎儿性别可能是胎盘对这些化学物质反应的重要修饰因素。对人类的研究表明BPA和邻苯二甲酸盐暴露与胎盘不良结局有关。展望未来,更多的研究应该在测量结果中考虑性别差异(称为“胎盘性别”),并应该利用适当的统计方法来评估胎儿性别的改变。此外,更一致的样本收集和分子结果评估范式将是在该领域取得进展不可或缺的。这些进步,以及用于测量胎盘功能和妊娠结局的改进的非侵入性工具,将对理解双酚a和邻苯二甲酸盐对胎盘表观遗传破坏的反应机制,以及这些破坏如何转化为胎盘和胎儿健康至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impacts of bisphenol A (BPA) and phthalate exposures on epigenetic outcomes in the human placenta.

The placenta guides fetal growth and development. Bisphenol A (BPA) and phthalates are widespread environmental contaminants and endocrine disruptors, and the placental epigenetic response to these chemicals is an area of growing research interest. Therefore, our objective was to summarize research linking BPA or phthalate exposure to placental outcomes in human pregnancies, with a particular focus on epigenetic endpoints. In PubMed, studies were selected for review (without limiting start date and ending on 1 May 2018) if they reported any direct effects of BPA or phthalates on the placenta in humans. Collectively, available studies suggest that BPA and phthalate exposures are associated with changes to placental micro-RNA expression, DNA methylation, and genomic imprinting. Furthermore, several studies suggest that fetal sex may be an important modifier of placental outcomes in response to these chemicals. Studies in humans demonstrate associations of BPA and phthalate exposure with adverse placental outcomes. Moving forward, more studies should consider sex differences (termed "placental sex") in the measured outcomes, and should utilize appropriate statistical approaches to assess modification by fetal sex. Furthermore, more consistent sample collection and molecular outcome assessment paradigms will be indispensable for making progress in the field. These advances, together with improved non-invasive tools for measuring placental function and outcomes across pregnancy, will be critical for understanding the mechanisms driving placental epigenetic disruption in response to BPA and phthalates, and how these disruptions translate into placental and fetal health.

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来源期刊
Environmental Epigenetics
Environmental Epigenetics GENETICS & HEREDITY-
CiteScore
6.50
自引率
5.30%
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0
审稿时长
17 weeks
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