Screening for Y chromosome microdeletions in idiopathic and nonidiopathic infertile men with varicocele and cryptorchidism

被引:0
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作者
Song, NH
Wu, HF [1 ]
Zhang, W
Zhuo, ZM
Qian, LX
Hua, LX
Guo, L
Feng, NH
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Urol, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Key Lab Reprod Med Jiangsu Province, Nanjing 210029, Peoples R China
[3] Nanjing Univ, Model Anim Res Ctr, Nanjing 210032, Peoples R China
关键词
Y chromosome; microdeletions; multiplex polymerase chain reaction; male infertility;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cytogenetic and molecular studies of azoospermic and oligozoospermic males have suggested the presence of azoospermia factors ( AZF) in the Y chromosome. Deletion in AZF regions has been reported to disrupt spermatogenesis and cause infertility. Several candidate genes responsible for spermatogenesis have been identified in this region and some of them are thought to be functional in human spermatogenesis. And we reported clinical and molecular studies of Y chromosome microdeletions in Chinese. This study aimed at assessing the frequency of microdeletions in Chinese men with idiopathic and nonidiopathic infertility problems and dicussing the clinical significance of the AZF region. Methods In this study, we screened 143 infertile men ( 62 with idiopathic infertilitas and 81 with nonidiopathic infertilitas), in whom karyotype, sperm count, hormonal parameters and fine needle aspiration cytology were evaluated. Genomic DNA was extracted from the peripheral leukocytes. Molecular analysis was performed by two multiplex polymerase chain reactions (PCR) using a set of a sequence tagged sites ( STS) from 3 different regions of the Y chromosome: AZFa ( sY84, sY86 AZFb ( sY127, sY134 AZFc ( sY254, sY255). Results Nineteen point four percent of idiopathic males ( 12/62, 19. 4%) had microdeletions of either the AZFa, AZFb, AZFc or AZFb + c region. Significantly, a high frequency of microdeletions (9/81, 11.1%) was found in nonidiopathic patients with varicocele and cryptorchidism. No deletions were found in healthy fertile men. There were no significant differences in the localization and extent of deletions between idiopathic and nonidiopathic patients. Conclusions The knowledge of the presence of these deletions in idiopathic and nonidiopathic cases is important to understand the prognosis, better management and counsel these patients accordingly. Furthermore, a more extended screening for Y chromosome microdeletions in idiopathic and nonidiopathic men, particularly candidates for intracytoplasmic sperm injection, is recommended.
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页码:1462 / 1467
页数:6
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