The role of epigenetics in male and female infertility

Q3 Medicine
D. A. Egorova, V. V. Derezina, M. V. Chebanyan, M. B. Sultonova, T. V. Ishmuratov, M. M. Gasanov, A. Z. Chipchikova, S. A. Paksileva, S. S. Mitkina, R. R. Khamidullina, A. S. Kutueva, A. A. Anikeeva
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Abstract

Introduction. Today, infertility is a global problem that affects about 48.5 million married couples worldwide. It has been suggested that epigenetic aberrations are of great importance for reproductive health, as they account for an interactive relationship between genomic landscape, interplay with gene environment and disease phenotype. A new understanding on etiology of complex non-Mendelian disease traits has aroused a growing interest in reproductive epigenetics.Aim: to analyze available publications on epigenetic aspects of male and female infertility as well as nutrition-related risk factors.Materials and Methods. There was conducted a search for publications in the electronic databases PubMed, Google Scholar and Library to be selected in accordance with PRISMA recommendations. All relevant articles published before November 2023 were included in this review. As a result of the search, there were extracted 530 publications from PubMed, 57 publications – from eLibrary and 23 publications – from Google Scholar. Duplicates and non-full-text article versions were excluded.Results. Environmental factors play an important role in generation and maintenance of epigenetic marks. DNA methylation abnormalities can lower human fertility. Altered protamine level may affect epigenetic paternally transmitted DNA information. Long-term infertility is associated with a modified methylome in euploid blastocysts primarily affecting regulation of genomic imprinting. Both excess and deficiency of trace elements are associated with adverse pregnancy outcomes, similarly applied infertility.Conclusion. Despite that epigenetic mechanisms, genes, nutrition and dietary supplements discussed here affect infertility, while a relevant recommended dose has not yet been determined, it was noted that such parameters may positively influence fertility. However, more comprehensive and longitudinal human studies are required to examine their relationship to male and female reproductive functions.
表观遗传学在男性和女性不孕症中的作用
导言。如今,不孕不育是一个全球性问题,影响着全球约 4850 万对已婚夫妇。有人认为,表观遗传畸变对生殖健康非常重要,因为它们是基因组景观、基因环境相互作用和疾病表型之间的互动关系。对复杂的非孟德尔疾病性状的病因学有了新的认识,这引起了人们对生殖表观遗传学的越来越大的兴趣。根据 PRISMA 建议,在 PubMed、Google Scholar 和 Library 等电子数据库中对出版物进行了检索。2023 年 11 月之前发表的所有相关文章均被纳入本综述。搜索结果显示,从 PubMed 中提取了 530 篇出版物,从电子图书馆中提取了 57 篇出版物,从谷歌学术中提取了 23 篇出版物。排除了重复和非全文版本的文章。环境因素在表观遗传标记的产生和维持中起着重要作用。DNA 甲基化异常会降低人类的生育能力。原胺水平的改变可能会影响表观遗传的父传 DNA 信息。长期不育与极性囊胚中甲基组的改变有关,主要影响基因组印记的调节。微量元素的过量和缺乏都与不良妊娠结局有关,这与不孕症的情况类似。尽管本文讨论的表观遗传学机制、基因、营养和膳食补充剂会影响不孕症,但相关的推荐剂量尚未确定,人们注意到这些参数可能会对生育产生积极影响。不过,还需要进行更全面的纵向人体研究,以考察它们与男性和女性生殖功能的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
68
审稿时长
12 weeks
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