Literature DB >> 28456595

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study.

Lingying Jiang1, Jiamin Jin1, Shasha Wang1, Fuxing Zhang1, Yongdong Dai1, Libing Shi1, Songying Zhang2.   

Abstract

A variety of experimental studies have yielded evidence that the cystic fibrosis transmembrane conductance regulator (CFTR) protein participates in the process of spermatogenesis. However, the association between CFTR gene and non-obstructive azoospermia (NOA) disease remained to be a question. First, we reviewed available data from the PubMed and Embase databases before May 2016 to find the most common mutations of CFTR gene in NOA patients. Second, an original case-control study was conducted on NOA patients (n=100) and a control group consisting of fertile males (n=100), selected from August 2015 to March 2017, to detect CFTR gene mutations and polymorphism. Peripheral blood samples from NOA patients and normal controls were analyzed for the presence of specific sequences of CFTR gene by polymerase chain reaction amplification followed by direct sequencing. From our comprehensive review, 12 case-control studies were found concerning the relation between CFTR gene mutations and polymorphism and NOA disease. Fifty-four mutations were mentioned and IVS8 poly-T, TG repeats, F508del and R117H mutations were the most common ones. Based on that, we detected IVS8 poly-T, TG repeats, F508del, R117H and M470V mutations in our case control study. We found that the T5 allele was present at a significantly higher rate in NOA patients than in the control group (5.00% versus 0.00%, p<0.01) with increased risk having NOA [Odds ratios (OR) 2.05, 95% confidence intervals (CI) 1.85-2.27]. The T5 variant was always accompanied by TG12 (10/10) and V470 allele participated in most TG12T5 haplotypes (8/10). TG12T5-V470 haplotype also enhanced risk of having NOA [OR 2.04, 95% CI 1.84-2.26]. F508del and R117H mutations were not found in either group. In conclusion, the polyvariant mutant genes of CFTR: T5 allele and TG12-T5-V470 genotype are correlated with NOA, but F508del and R117H mutations have low possibility to be associated with NOA.
Copyright © 2017. Published by Elsevier B.V.

Entities:  

Keywords:  F508del; IVS8 poly-T; M470V; Non-obstructive azoospermia; R117H; TG repeats

Mesh:

Substances:

Year:  2017        PMID: 28456595     DOI: 10.1016/j.gene.2017.04.044

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  8 in total

1.  Localization of epithelial sodium channel (ENaC) and CFTR in the germinal epithelium of the testis, Sertoli cells, and spermatozoa.

Authors:  Sachin Sharma; Aaron Hanukoglu; Israel Hanukoglu
Journal:  J Mol Histol       Date:  2018-02-16       Impact factor: 2.611

Review 2.  Male Infertility in Humans: An Update on Non-obstructive Azoospermia (NOA) and Obstructive Azoospermia (OA).

Authors:  Xiaolong Wu; Dengfeng Lin; Fei Sun; C Yan Cheng
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

3.  The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia.

Authors:  Leyla Jafari; Kyumars Safinejad; Mahboobeh Nasiri; Mansour Heidari; Massoud Houshmand
Journal:  J Med Life       Date:  2022-04

4.  Two novel and correlated CF-causing insertions in the (TG)mTn tract of the CFTR gene.

Authors:  Silvia Pierandrei; Giovanna Blaconà; Benedetta Fabrizzi; Giuseppe Cimino; Natalia Cirilli; Nicole Caporelli; Antonio Angeloni; Marco Cipolli; Marco Lucarelli
Journal:  PLoS One       Date:  2019-10-08       Impact factor: 3.240

5.  Evaluation of association between methylenetetrahydrofolate reductase and azoospermia: A meta-analysis.

Authors:  Guang-Xing Tan; Lin Jiang; Gang-Qin Li; Kuan Bai
Journal:  Medicine (Baltimore)       Date:  2021-04-16       Impact factor: 1.817

6.  A Catalog of Human Genes Associated With Pathozoospermia and Functional Characteristics of These Genes.

Authors:  Elena V Ignatieva; Alexander V Osadchuk; Maxim A Kleshchev; Anton G Bogomolov; Ludmila V Osadchuk
Journal:  Front Genet       Date:  2021-07-05       Impact factor: 4.599

7.  Gene therapy-emulating small molecule treatments in cystic fibrosis airway epithelial cells and patients.

Authors:  Q Yang; A R Soltis; G Sukumar; X Zhang; H Caohuy; J Freedy; C L Dalgard; M D Wilkerson; H B Pollard; B S Pollard
Journal:  Respir Res       Date:  2019-12-21

8.  Cystic fibrosis gene mutations and polymorphisms in Saudi men with infertility.

Authors:  Talal AlMaghamsi; Naeem Iqbal; Nabil Abdullrahman Al-Esaei; Muhsina Mohammed; Kamel Zein Eddin; Fatima Ghurab; Nabil Moghrabi; Emily Heaphy; Islam Junaid
Journal:  Ann Saudi Med       Date:  2020-08-06       Impact factor: 1.526

  8 in total

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