Micronucleus counts correlating with male infertility: a clinical analysis of chromosomal abnormalities and reproductive parameters.
- Author:
Shun-Han ZHANG
1
;
Ying-Jun XIE
;
Wen-Jun QIU
;
Qian-Ying PAN
;
Li-Hao CHEN
;
Jian-Feng WU
;
Si-Qi HUANG
;
Ding WANG
;
Xiao-Fang SUN
Author Information
- Publication Type:Journal Article
- Keywords: chromosome instability; genetic azoospermia; male infertility; micronucleus; semen parameters
- MeSH: Humans; Male; Infertility, Male/genetics*; Adult; Micronucleus Tests; Semen Analysis; Oligospermia/genetics*; Azoospermia/genetics*; Chromosome Aberrations; Sperm Count; Micronuclei, Chromosome-Defective; Middle Aged
- From: Asian Journal of Andrology 2025;27(4):537-542
- CountryChina
- Language:English
- Abstract: 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.
