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女性不孕症遗传病因学的进展。

Advances in the genetic etiology of female infertility.

作者信息

Gu Ruihuan, Wu Tianyu, Fu Jing, Sun Yi-Juan, Sun Xiao-Xi

机构信息

Department of Shanghai Ji'ai Genetics and IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, 352 Dalin Road, Shanghai, 200011, China.

Institute of Pediatrics, State Key Laboratory of Genetic Engineering, Institutes of BiomedicalSciences, Shanghai Key Laboratory of Medical Epigenetics, Children's Hospital of Fudan University, Fudan University, Shanghai, 200032, China.

出版信息

J Assist Reprod Genet. 2024 Dec;41(12):3261-3286. doi: 10.1007/s10815-024-03248-w. Epub 2024 Sep 25.

Abstract

Human reproduction is a complex process involving gamete maturation, fertilization, embryo cleavage and development, blastocyst formation, implantation, and live birth. If any of these processes are abnormal or arrest, reproductive failure will occur. Infertility is a state of reproductive dysfunction caused by various factors. Advances in molecular genetics, including cell and molecular genetics, and high-throughput sequencing technologies, have found that genetic factors are important causes of infertility. Genetic variants have been identified in infertile women or men and can cause gamete maturation arrest, poor quality gametes, fertilization failure, and embryonic developmental arrest during assisted reproduction technology (ART), and thus reduce the clinical success rates of ART. This article reviews clinical studies on repeated in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) failures caused by ovarian dysfunction, oocyte maturation defects, oocyte abnormalities, fertilization disorders, and preimplantation embryonic development arrest due to female genetic etiology, the accumulation of pathogenic genes and gene pathogenic loci, and the functional mechanism and clinical significance of pathogenic genes in gametogenesis and early embryonic development.

摘要

人类生殖是一个复杂的过程,涉及配子成熟、受精、胚胎分裂与发育、囊胚形成、着床以及分娩。如果这些过程中的任何一个出现异常或停滞,就会发生生殖失败。不孕症是由多种因素导致的生殖功能障碍状态。分子遗传学的进展,包括细胞和分子遗传学以及高通量测序技术,已经发现遗传因素是不孕症的重要原因。在不孕女性或男性中已经鉴定出遗传变异,这些变异可导致配子成熟停滞、配子质量差、受精失败以及辅助生殖技术(ART)期间的胚胎发育停滞,从而降低ART的临床成功率。本文综述了关于女性遗传病因导致的卵巢功能障碍、卵母细胞成熟缺陷、卵母细胞异常、受精障碍以及植入前胚胎发育停滞引起的反复体外受精(IVF)/卵胞浆内单精子注射(ICSI)失败的临床研究,致病基因和基因致病位点的积累,以及致病基因在配子发生和早期胚胎发育中的功能机制和临床意义。

相似文献

1
Advances in the genetic etiology of female infertility.女性不孕症遗传病因学的进展。
J Assist Reprod Genet. 2024 Dec;41(12):3261-3286. doi: 10.1007/s10815-024-03248-w. Epub 2024 Sep 25.

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