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Vol 78, No 8 (2007)
ARTICLES
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The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia

Ryszard Ślęzak, Małgorzata Szczepaniak, Magdalena Pasińska, Halina Czemarmazowicz
Ginekol Pol 2007;78(8).

open access

Vol 78, No 8 (2007)
ARTICLES

Abstract

Mutations in cystic fibrosis transductance regulator gene (CFTR ) are known to result in some forms of male infertility. An association between CFTR gene mutations and obstructive azoospermia in cystic fibrosis (CF) and in congenital unilateral and bilateral absence of vas deferens (CUAVD, CBAVD) has been proven. However, the role of CFTR gene mutations in the etiology of non-obstructive azoospermia, as well as in the regulation of spermatogenesis remains unsolved. Objectives: The aim of the study was to evaluate the frequency of CFTR mutations in patients diagnosed with different forms of spermatogenesis impairment Material: The molecular analyses were performed in the group of 93 infertile men, diagnosed with either azoospermia, oligospermia or asthenoteratozoospermia. Results: The results of the study revealed the presence of F508del and IVS8-T in 5,4% of analyzed cases. No difference in CFTR gene mutations frequencies among patients with azoospermia, oligospermia and asthenoteratozoospermia has been observed. Conclusion: The CFTR gene mutations frequency in men with nonobstructive azoospermia, oligozoospermia and asthenozoospermia is similar to those observed in general population.

Abstract

Mutations in cystic fibrosis transductance regulator gene (CFTR ) are known to result in some forms of male infertility. An association between CFTR gene mutations and obstructive azoospermia in cystic fibrosis (CF) and in congenital unilateral and bilateral absence of vas deferens (CUAVD, CBAVD) has been proven. However, the role of CFTR gene mutations in the etiology of non-obstructive azoospermia, as well as in the regulation of spermatogenesis remains unsolved. Objectives: The aim of the study was to evaluate the frequency of CFTR mutations in patients diagnosed with different forms of spermatogenesis impairment Material: The molecular analyses were performed in the group of 93 infertile men, diagnosed with either azoospermia, oligospermia or asthenoteratozoospermia. Results: The results of the study revealed the presence of F508del and IVS8-T in 5,4% of analyzed cases. No difference in CFTR gene mutations frequencies among patients with azoospermia, oligospermia and asthenoteratozoospermia has been observed. Conclusion: The CFTR gene mutations frequency in men with nonobstructive azoospermia, oligozoospermia and asthenozoospermia is similar to those observed in general population.
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Keywords

infertility male, chromosome - aberrations, Mutation

About this article
Title

The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia

Journal

Ginekologia Polska

Issue

Vol 78, No 8 (2007)

Bibliographic record

Ginekol Pol 2007;78(8).

Keywords

infertility male
chromosome - aberrations
Mutation

Authors

Ryszard Ślęzak
Małgorzata Szczepaniak
Magdalena Pasińska
Halina Czemarmazowicz

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