男性不孕症及其与下一代测序的联系,作为一条通往确定的诊断的新途径
Maryam Afkari1, Samaneh Saboori-Darabi2, Seyed Abolhassan Shahzadeh Fazeli3
1Department of Developmental Biology, Faculty of Basic Sciences and Advanced Technologies in Biology, University of Science and Culture, ACECR, Tehran, Iran; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, P.O. Box: 16635-148, Tehran, Iran.
Gene
|July 5, 2025
概括
数以百万计的夫妇面临不孕不育,男性因素在很大程度上发挥了作用. 基因研究,特别是使用下一代测序,旨在确定男性不孕症的新原因并改善诊断.
科学领域:
- 人类遗传学 人类遗传学
- 生殖医学 生殖医学
- 基因组医学是基因组医学.
背景情况:
- 男性不孕症影响全球数百万,遗传因素在其复杂的病因学中起着至关重要的作用.
- 大约4%的不育男性有已知的遗传原因,而绝大多数 (60-70%) 仍然无法解释.
- 目前有100多个基因与男性不孕症有关,估计有2000个基因有助于胚胎细胞的发育和半转化.
研究的目的:
- 识别与男性生育能力相关的新型因果基因和变异.
- 通过改进的遗传面板来增强男性不孕症的诊断能力.
- 为了减少无法解释的男性不孕不育病例的发生率.
主要方法:
- 审查目前的男性不孕症遗传诊断技术.
- 强调下一代测序 (NGS) 的作用和影响越来越大.
- 与传统的方法比较,如型定型,Y染色体查和微阵列分析.
主要成果:
- 下一代测序 (NGS) 显著加速了新男性不育基因的发现.
- NGS导致了用于诊断男性不孕症的遗传面板的扩展.
- 遗传因素越来越被认为是男性不孕症的关键组成部分.
结论:
- NGS正在彻底改变男性不孕症的诊断和理解.
- 持续的遗传研究对于揭开男性不孕不育的剩余不明原因的病例至关重要.
- 改进的基因诊断有望改善患者管理和生殖结果.
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