Dai Bai, Zhao Dan, Sha Ri-Na, Cang Ming
Reproductive Medicine Center, the Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.
State Key Laboratory of Reproduction and Breeding in Grassland Livestock, Inner Mongolia University, Hohhot, China.
Transl Androl Urol. 2025 Mar 30;14(3):619-626. doi: 10.21037/tau-24-593. Epub 2025 Mar 26.
Infertility significantly impacts numerous couples worldwide, and male infertility is a common contributing factor. Y chromosome microdeletions are potential genetic causes of male infertility. However, due to the lack of comparative studies based on semen analysis results, we have difficulty selecting an appropriate method for detecting Y chromosome microdeletions. This study aims to compare the application of high-throughput sequencing and fluorescence quantitative polymerase chain reaction (qPCR) in different types of infertility patients.
This study used high-throughput sequencing [next-generation sequencing (NGS)] and fluorescence qPCR methods to detect Y chromosome microdeletions in two groups: one with azoospermia and another with oligoasthenoteratozoospermia (OAT), characterized by reduced sperm count and motility.
The results showed that NGS identified cases of Klinefelter syndrome (congenital bilateral absence of the vas deferens) that were not detected by qPCR in the azoospermia group. In the OAT group, high-throughput sequencing found a b2/b3 deletion of 1.80 Mb, while qPCR did not detect it. Conversely, qPCR identified an AZFd deletion in the OAT group, missed by high-throughput sequencing due to inadequate target region coverage.
These research findings are significant for guiding personalized treatment of male infertility patients and provide valuable references for further exploration of the association between Y chromosome microdeletions and male infertility.
不孕症对全球众多夫妇产生重大影响,男性不育是一个常见的促成因素。Y染色体微缺失是男性不育的潜在遗传原因。然而,由于缺乏基于精液分析结果的比较研究,我们在选择检测Y染色体微缺失的合适方法时存在困难。本研究旨在比较高通量测序和荧光定量聚合酶链反应(qPCR)在不同类型不育症患者中的应用。
本研究采用高通量测序[下一代测序(NGS)]和荧光定量PCR方法,对两组患者进行Y染色体微缺失检测:一组为无精子症患者,另一组为少弱畸精子症(OAT)患者,其特征为精子数量减少和活力降低。
结果显示,在无精子症组中,NGS检测出了qPCR未检测到的克兰费尔特综合征(先天性双侧输精管缺如)病例。在OAT组中,高通量测序发现了一个1.80 Mb的b2/b3缺失,而qPCR未检测到。相反,qPCR在OAT组中检测到了一个AZFd缺失,由于目标区域覆盖不足,高通量测序未检测到。
这些研究结果对指导男性不育患者的个性化治疗具有重要意义,并为进一步探索Y染色体微缺失与男性不育之间的关联提供了有价值的参考。