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PMID: 16257105 Published · ppublish English

The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.

Zhoucun A, Zhang Sizhong, Yang Yuan, Ma Yongxin, Zhang Wei, Lin Li

Abstract

To explore the possible association between the common single nucleotide polymorphism N372H in human breast cancer susceptibility gene 2 (BRCA2) and the idiopathic male infertility with azoospermia or severe oligozoospermia.,The study included 240 infertile patients with idiopathic azoospermia or severe oligozoospermia and 250 fathered controls. The allele and genotype frequencies of the polymorphism N372H in BRCA2 gene were investigated in both patients and controls using denaturing high performance liquid chromatography analysis (DHPLC).,The frequency of allele H of the polymorphism N372H in patients was significantly higher than that of the controls (23.5% versus 17.6%, OR = 1.49, 95% CI 1.06-1.97, P = 0.02) and the subjects bearing rare allele H (NH + HH) significantly increased in patients compared with controls (41.7% versus 32.4%, 95% CI 1.03-2.15, P = 0.03).,The results of this study suggested that the polymorphism N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.

Article Info
Journal
European journal of obstetrics, gynecology, and reproductive biology
Abbr.
Eur J Obstet Gynecol Reprod Biol
Published
2006-02-17
Indexed
2006-01-02
Updated
2006-11-15
Language
English
Country/Region
Ireland
NLM ID
0375672
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