Literature DB >> 16157049

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

Ning-hong Song1, Hong-fei Wu, Wei Zhang, Zuo-min Zhuo, Li-xing Qian, Li-xing Hua, Lin Guo, Ning-han Feng.   

Abstract

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.

Entities:  

Mesh:

Year:  2005        PMID: 16157049

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  6 in total

Review 1.  Genetics and epigenetics of varicocele pathophysiology: an overview.

Authors:  Viviane Paiva Santana; Cristiana Libardi Miranda-Furtado; Flavia Gaona de Oliveira-Gennaro; Rosana Maria Dos Reis
Journal:  J Assist Reprod Genet       Date:  2017-05-18       Impact factor: 3.412

2.  Molecular and cytogenetic studies of 101 infertile men with microdeletions of Y chromosome in 1,306 infertile Korean men.

Authors:  Min Jee Kim; Hye Won Choi; So Yeon Park; In Ok Song; Ju Tae Seo; Hyoung-Song Lee
Journal:  J Assist Reprod Genet       Date:  2012-03-29       Impact factor: 3.412

3.  Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.

Authors:  Songchang Chen; Qian Zhang; Liming Chu; Chunxin Chang; Yiyao Chen; Zhongwei Bao; Weihua Peng; Lanlan Zhang; Shuyuan Li; Chao Liu; Huanhuan Zhu; Feng Yu; Xiaoyan Chen; Lili Jiang; Daru Lu; Zhengwen Jiang; Li Jin; Chenming Xu
Journal:  J Hum Genet       Date:  2021-08-31       Impact factor: 3.172

4.  Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip.

Authors:  Ashraf J Shaqalaih; Masood S Abu Halima; Mohammed J Ashour; Fadel A Sharif
Journal:  J Exp Clin Assist Reprod       Date:  2009-10-20

5.  The significance of Y chromosome microdeletion analysis in subfertile men with clinical variocele.

Authors:  Levent Sagnak; Hamit Ersoy; Ugur Ozok; Asir Eraslan; Kanay Yararbas; Goksel Goktug; Ajlan Tukun
Journal:  Arch Med Sci       Date:  2010-06-30       Impact factor: 3.318

6.  The prevalence of chromosomal deletions relating to developmental delay and/or intellectual disability in human euploid blastocysts.

Authors:  Wenyin He; Xiaofang Sun; Lian Liu; Man Li; Hua Jin; Wei-Hua Wang
Journal:  PLoS One       Date:  2014-01-07       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.