M L N Deepika, Avvari Srilekha, C Lalitha Pavani, Aryan Gupta, Ridah Nazneen, B Vijaya Lakshmi
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引用次数: 0
摘要
复发性妊娠流产(RPL)是指两次或两次以上的妊娠在达到存活期之前自然流产。复发性妊娠流产夫妇的诊断通常只涉及女性伴侣。然而,由于 Y 染色体中含有多个控制精子发生和精子质量的基因,因此男性伴侣同样会导致自然流产的发生。据报道,Y 染色体远半部分的三个非重叠区(AZFa、AZFb 和 AZFc)与核型正常男性的精子发生有关。在许多反复流产的男性伴侣中发现了这三个区域的微缺失。Y 染色体的 STS 区域容易发生自我重组,因此容易发生缺失,从而导致精子质量差和胎儿植入失败。本研究旨在确定 RPL 女性男性伴侣中微缺失的频率和类型。分析表明,近 76% 的病例显示 Y 染色体存在微缺失,而对照组中未观察到缺失,这表明 RPL 与男性伴侣 Y 染色体 AZF 区的微缺失之间存在密切联系。
Prevalence and comparative analysis of Y chromosome microdeletions in recurrent pregnancy loss.
Recurrent pregnancy loss (RPL) is defined as the spontaneous loss of two or more pregnancies before reaching viability. Diagnosis for couples with RPL usually involves only the female partner. However, it is seen that male partners contribute equally to the occurrence of spontaneous abortions as the Y chromosome harbors several genes that control spermatogenesis and the quality of sperms. Three non-overlapping regions (AZFa, AZFb, AZFc) in the distal half of Y chromosome have been reported to be associated with spermatogenesis in males with normal karyotype. Microdeletions in these three regions have been identified in many male partners with repeated abortions. The STS regions of the Y chromosome are prone to self-recombination, making it susceptible to deletions, thereby leading to poor sperm quality and fetal implantation failure. The present study aimed to identify the frequency and type of microdeletions among male partners of RPL women. Analysis revealed nearly 76% of cases revealed microdeletions, whereas no deletions were observed among controls in Y chromosome, suggesting a strong link between RPL and microdeletion in the AZF regions of the Y chromosome in the male partner.
期刊介绍:
The Journal of Applied Genetics is an international journal on genetics and genomics. It publishes peer-reviewed original papers, short communications (including case reports) and review articles focused on the research of applicative aspects of plant, human, animal and microbial genetics and genomics.