Zhang Shun-Han, Xie Ying-Jun, Qiu Wen-Jun, Pan Qian-Ying, Chen Li-Hao, Wu Jian-Feng, Huang Si-Qi, Wang Ding, Sun Xiao-Fang
Department of Obstetrics and Gynecology, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine, The Third Affiliated Hospital, Guangzhou Medical University, Guangzhou 510150, China.
Asian J Androl. 2025 Jul 1;27(4):537-542. doi: 10.4103/aja2024103. Epub 2025 Jan 10.
Investigating the correlation between micronucleus formation and male infertility has the potential to improve clinical diagnosis and deepen our understanding of pathological progression. Our study enrolled 2252 male patients whose semen was analyzed from March 2023 to July 2023. Their clinical data, including semen parameters and age, were also collected. Genetic analysis was used to determine whether the sex chromosome involved in male infertility was abnormal (including the increase, deletion, and translocation of the X and Y chromosomes), and subsequent semen analysis was conducted for clinical grouping purposes. The participants were categorized into five groups: normozoospermia, asthenozoospermia, oligozoospermia, oligoasthenozoospermia, and azoospermia. Patients were randomly selected for further study; 41 patients with normozoospermia were included in the control group and 117 patients with non-normozoospermia were included in the study group according to the proportions of all enrolled patients. Cytokinesis-block micronucleus (CBMN) screening was conducted through peripheral blood. Statistical analysis was used to determine the differences in micronuclei (MNi) among the groups and the relationships between MNi and clinical data. There was a significant increase in MNi in infertile men, including those with azoospermia, compared with normozoospermic patients, but there was no significant difference between the genetic and nongenetic groups in azoospermic men. The presence of MNi was associated with sperm concentration, progressive sperm motility, immotile spermatozoa, malformed spermatozoa, total sperm count, and total sperm motility. This study underscores the potential utility of MNi as a diagnostic tool and highlights the need for further research to elucidate the underlying mechanisms of male infertility.
研究微核形成与男性不育之间的相关性,有可能改善临床诊断并加深我们对病理进展的理解。我们的研究纳入了2252名男性患者,他们的精液在2023年3月至2023年7月期间进行了分析。还收集了他们的临床数据,包括精液参数和年龄。采用基因分析来确定参与男性不育的性染色体是否异常(包括X和Y染色体的增加、缺失和易位),随后为临床分组目的进行了精液分析。参与者被分为五组:正常精子症、弱精子症、少精子症、少弱精子症和无精子症。随机选择患者进行进一步研究;根据所有纳入患者的比例,41名正常精子症患者被纳入对照组,117名非正常精子症患者被纳入研究组。通过外周血进行胞质分裂阻滞微核(CBMN)筛查。采用统计分析来确定各组之间微核(MNi)的差异以及MNi与临床数据之间的关系。与正常精子症患者相比,不育男性(包括无精子症患者)的MNi显著增加,但无精子症男性的遗传组和非遗传组之间没有显著差异。MNi的存在与精子浓度、进行性精子活力、不动精子、畸形精子、总精子计数和总精子活力有关。本研究强调了MNi作为诊断工具的潜在效用,并突出了进一步研究以阐明男性不育潜在机制的必要性。