Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia

被引:70
作者
Kherraf, Zine-Eddine [1 ,2 ]
Cazin, Carolin [1 ,2 ,7 ]
Bouker, Amine [3 ]
Ben Mustapha, Selima Fourati [3 ]
Hennebicq, Sylviane [1 ,4 ]
Septier, Amandine [5 ]
Coutton, Charles [1 ,6 ]
Raymond, Laure [7 ]
Nouchy, Marc [7 ]
Thierry-Mieg, Nicolas [5 ]
Zouari, Raoudha [3 ]
Arnoult, Christophe [1 ]
Ray, Pierre F. [1 ,2 ]
机构
[1] Univ Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Inst Adv Biosci Team Genet Epigenet & Therap, F-38000 Grenoble, France
[2] CHU Grenoble Alpes, UM GI DPI, F-38000 Grenoble, France
[3] Ctr Urbain Nord, Polyclin Jasmins, Ctr Aide Med Procreat, Tunis 1003, Tunisia
[4] CHU Grenoble Alpes, Lab Daide Procreation CECOS, F-38000 Grenoble, France
[5] Univ Grenoble Alpes, CNRS, TIMC, F-38000 Grenoble, France
[6] CHU Grenoble Alpes, Genetiq Chromosom, F-38000 Grenoble, France
[7] Lab Euro Fins Biomnis, Dept Genet Mol, F-69007 Lyon, France
关键词
PREMATURE OVARIAN INSUFFICIENCY; CHROMOSOME SYNAPSIS; VARIANTS; INFERTILITY; MUTATIONS; DEFECTS; DMC1; GENE; MSH5;
D O I
10.1016/j.ajhg.2022.01.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Non-obstructive azoospermia (NOA) is a severe and frequent cause of male infertility, often treated by testicular sperm extraction followed by intracytoplasmic sperm injection. The aim of this study is to improve the genetic diagnosis of NOA, by identifying new genes involved in human NOA and to better assess the chances of successful sperm extraction according to the individual's genotype. Exome sequencing was performed on 96 NOA-affected individuals negative for routine genetic tests. Bioinformatics analysis was limited to a panel of 151 genes selected as known causal or candidate genes for NOA. Only highly deleterious homozygous or hemizygous variants were retained as candidates. A likely causal defect was identified in 16 genes in a total of 22 individuals (23%). Six genes had not been described in man (DDX25, HENMT1, MCMDC2, MSH5, REC8, TDRKH) and 10 were previously reported (C14orf39, DMC1, FANCM, GCNA, HFM1, MCM8, MEIOB, PDHA2, TDRD9, TERB1). Seven individuals had defects in genes from piwi or DNA repair pathways, three in genes involved in post-meiotic maturation, and 12 in meiotic processes. Interestingly, all individuals with defects in meiotic genes had an unsuccessful sperm retrieval, indicating that genetic diagnosis prior to TESE could help identify individuals with low or null chances of successful sperm retrieval and thus avoid unsuccessful surgeries.
引用
收藏
页码:508 / 517
页数:11
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