Literature DB >> 18062861

Gene polymorphisms and male infertility--a meta-analysis and literature review.

Frank Tüttelmann1, Ewa Rajpert-De Meyts, Eberhard Nieschlag, Manuela Simoni.   

Abstract

Many genetic polymorphisms have been studied extensively to elucidate their role in the pathophysiology of male infertility. This article presents a review of the literature following a thorough search of PubMed, a compilation of meta-analyses of studies reporting an association with male fertility where the population(s) could be clearly identified as fertile and/or infertile, and a summary of all polymorphisms that have been investigated in single case-control studies to date. The meta-analyses revealed significant associations between polymorphism and male fertility only for AZF gr/gr deletions (OR 1.81, 1.46-2.24 CI, P<0.00001) and MTHFR 677C-->T (OR 1.39, 1.15-2.69 95% CI, P=0.0006) but not for POLG, DAZL, USP26 or FSHR. The influence of CAG repeat length in AR remains open and debated. Genes encoding nuclear proteins (PRM1/2, TNP1/2) and ER1 are possible candidates for further examination, while the role of TAF7L remains unclear. Polymorphisms in 16 other genes have been investigated in single studies, but the results remain doubtful due to often small and heterogeneous cohorts and in the absence of independent replications. The genetic studies performed so far emphasize the complexity of male infertility as a presumably polygenetic trait amended by environmental, lifestyle or occupational factors.

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Year:  2007        PMID: 18062861     DOI: 10.1016/s1472-6483(10)60531-7

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  70 in total

1.  A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.

Authors:  Han Zhao; Jianfeng Xu; Haobo Zhang; Jielin Sun; Yingpu Sun; Zhong Wang; Jiayin Liu; Qiang Ding; Shaoming Lu; Rong Shi; Li You; Yingying Qin; Xiaoming Zhao; Xiaoling Lin; Xiao Li; Junjie Feng; Li Wang; Jeffrey M Trent; Chengyan Xu; Ying Gao; Bo Zhang; Xuan Gao; Jingmei Hu; Hong Chen; Guangyu Li; Junzhao Zhao; Shuhua Zou; Hong Jiang; Cuifang Hao; Yueran Zhao; Jinglong Ma; S Lilly Zheng; Zi-Jiang Chen
Journal:  Am J Hum Genet       Date:  2012-04-26       Impact factor: 11.025

2.  AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.

Authors:  Steven G Rozen; Janet D Marszalek; Kathryn Irenze; Helen Skaletsky; Laura G Brown; Robert D Oates; Sherman J Silber; Kristin Ardlie; David C Page
Journal:  Am J Hum Genet       Date:  2012-10-25       Impact factor: 11.025

Review 3.  A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART).

Authors:  Eisa Tahmasbpour; Dheepa Balasubramanian; Ashok Agarwal
Journal:  J Assist Reprod Genet       Date:  2014-08-13       Impact factor: 3.412

4.  Partial Deletions of Y-Chromosome in Infertile Men with Non-obstructive Azoospermia and Oligoasthenoteratozoospermia in a Turkish Population.

Authors:  Cemallettin Cengiz Beyaz; Sezgin Gunes; Kadir Onem; Tuba Kulac; Ramazan Asci
Journal:  In Vivo       Date:  2017 May-Jun       Impact factor: 2.155

Review 5.  [Genetics of male infertility].

Authors:  F Tüttelmann; J Gromoll; S Kliesch
Journal:  Urologe A       Date:  2008-12       Impact factor: 0.639

6.  Genetic study of Hormad1 and Hormad2 with non-obstructive azoospermia patients in the male Chinese population.

Authors:  Bing Song; Xiaojin He; Weidong Du; Yan Zhang; Jian Ruan; Fusheng Zhou; Xian-bo Zuo; Huan Wu; Xing Zha; Shuhua Liu; Xu-shi Xie; Lei Ye; Zhaolian Wei; Ping Zhou; Yun-xia Cao
Journal:  J Assist Reprod Genet       Date:  2014-05-07       Impact factor: 3.412

7.  FSHR single nucleotide polymorphism frequencies in proven fathers and infertile men in Southeast Turkey.

Authors:  Mahmut Balkan; Abdullah Gedik; Hasan Akkoc; Ozlem Izci Ay; M Emin Erdal; Hilmi Isi; Turgay Budak
Journal:  J Biomed Biotechnol       Date:  2010-04-29

8.  Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background.

Authors:  C Krausz; C Giachini; Y Xue; M K O'Bryan; J Gromoll; E Rajpert-de Meyts; R Oliva; I Aknin-Seifer; E Erdei; N Jorgensen; M Simoni; J L Ballescà; R Levy; G Balercia; P Piomboni; E Nieschlag; G Forti; R McLachlan; C Tyler-Smith
Journal:  J Med Genet       Date:  2008-09-09       Impact factor: 6.318

9.  Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory.

Authors:  Deborah Lo Giacco; Chiara Chianese; Josvany Sánchez-Curbelo; Lluis Bassas; Patricia Ruiz; Osvaldo Rajmil; Joaquim Sarquella; Alvaro Vives; Eduard Ruiz-Castañé; Rafael Oliva; Elisabet Ars; Csilla Krausz
Journal:  Eur J Hum Genet       Date:  2013-11-06       Impact factor: 4.246

10.  Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.

Authors:  Celia Ravel; Sandra Chantot-Bastaraud; Clementine Chalmey; Luis Barreiro; Isabelle Aknin-Seifer; Jerome Pfeffer; Isabelle Berthaut; E Emmanuelle Mathieu; Jacqueline Mandelbaum; Jean-Pierre Siffroi; Ken McElreavey; Anu Bashamboo
Journal:  PLoS One       Date:  2009-08-06       Impact factor: 3.240

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