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The role of CFTR p.G970D missense mutation in male infertility


1 Center for Advanced Studies and Technology (CAST), G. d'Annunzio University of Chieti-Pescara, Chieti 66100, Italy
2 Department of Psychological Health and Territory Science, School of Medicine and Health Sciences, G. d'Annunzio University of Chieti-Pescara, Chieti 66100, Italy

Date of Submission03-Jun-2022
Date of Acceptance21-Jun-2022
Date of Web Publication26-Jul-2022

Correspondence Address:
Ivana Antonucci,
Center for Advanced Studies and Technology (CAST), G. d'Annunzio University of Chieti-Pescara, Chieti 66100; Department of Psychological Health and Territory Science, School of Medicine and Health Sciences, G. d'Annunzio University of Chieti-Pescara, Chieti 66100
Italy

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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/aja202260

PMID: 35899923


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How to cite this URL:
Antonucci I, Angilletta I, Anaclerio F. The role of CFTR p.G970D missense mutation in male infertility. Asian J Androl [Epub ahead of print] [cited 2022 Oct 3]. Available from: https://www.ajandrology.com/preprintarticle.asp?id=352413

Over the years, accumulating evidence has confirmed the crucial role of cystic fibrosis transmembrane conductance regulator (CFTR) mutations in male infertility caused by congenital bilateral absence of the vas deferens (CBAVD), the most common cause of obstructive azoospermia (OA).[1],[2] The distribution and frequency of CFTR mutations in CBAVD patients vary considerably across countries and ethnic groups, and this suggests the need to develop regional variant panels to significantly improve diagnosis and management of infertile males. Anyway, it is surprising that alterations in the CFTR gene may also influence spermatogenesis and sperm quality, suggesting the crucial role of a correct genotype–phenotype correlation in CFTR-related disorders (CFTR-RD). Based on this evidence, genetic counseling is particularly important to estimate the risks of having an affected child with chronic or severe diseases and to discuss the impact of novel CFTR variants on reproductive health.

In the recent issue of Asian Journal of Andrology, Hou et al.[3] investigated the relationship between loss-of-function CFTR p.G970D missense variant and male infertility. First, the authors identified the presence of the homozygous p.G970D variant in a patient with CBAVD and nonobstructive azoospermia (NOA). Several studies have reported an increased frequency of the CFTR mutation in NOA and severe oligozoospermia. There are some concrete evidence to support the hypothesis that CFTR proteins can affect spermatogenic function and sperm quality.[4] The impairment in CFTR protein quantity or quality varies widely based on genetic mutation class and type.[5] However, further investigation is needed to confirm this aspect. Second, the authors conducted a retrospective analysis of Chinese patients with CBAVD and showed that p.G970D is a common pathogenic variant in infertile male patients. Taken together, these findings provide evidence that ethnicity/geography affects the frequency and spectrum of CFTR mutations in CBAVD patients. In this context, a population-specific panel should be designed to provide precise molecular diagnosis to couples before undergoing assisted reproductive technologies (ART). To this regard, the identification of novel CFTR variants in these couples has important implications for genetic counseling. In fact, the estimate of the risk of having children with CFTR mutations is crucial for the reproductive choice of future parents. The data are interesting regarding functional genomics studies to verify the effects of CFTR p.G970D mutations on spermatogenesis. In particular, the authors have generated CFTR p.G970D-mutated cell models using the clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) technology. In vitro data obtained are interesting, and p.G970D mutation may affect the proliferation of spermatocytes and Sertoli cells. In addition, this novel variant might influence CFTR expression and alter CFTR RNA splicing in spermatocytes. These important results demonstrate for the first time that CFTR p.G970D mutation is associated with disrupted spermatogenesis, especially during the early stage. From a practical clinical point of view, these data suggest usefulness of extending CFTR testing to other categories of infertile men, in particular patients with severe oligozoospermia or with reduced ejaculate volume. Although the role of this mutation in azoospermia requires confirmation in a larger patient cohort, it would be appropriate to include this variant in the routine CFTR screening not only in Chinese men with CBAVD but also in populations outside of China. In this scenario, molecular diagnostic based on sequencing of the entire CFTR gene followed by MPLA analysis could be considered for genetic analysis in Chinese patients.[6] Finally, the authors highlighted some limitations in their article: (i) the insufficient sample size; and (ii) more evidence needed to clarify the function of p.G970D variant. In view of these considerations, further studies should be conducted to confirm these interesting data in the future.

Based on this new insight, the identification of novel pathogenic variants emphasizes the importance of regional diagnostic protocols to improve medical and genetic care of infertile men.


  Competing Interests Top


All authors declare no competing interests.



 
  References Top

1.
Stuppia L, Antonucci I, Binni F, Brandi A, Grifone N, et al. Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. Eur J Hum Genet 2005; 13: 959–64.  Back to cited text no. 1
    
2.
Giuliani R, Antonucci I, Torrente I, Grammatico P, Palka G, et al. Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols. Asian J Androl 2010; 12: 819–26.  Back to cited text no. 2
    
3.
Hou JW, Li XL, Wang L, Dai CL, Li N, et al. Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis. Asian J Androl 2022; Doi: 10.4103/aja202236. [Online ahead of print].  Back to cited text no. 3
    
4.
Li Q, Shen Y, Zhao LJ, Wang JB, Huang X. Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF. Andrologia 2022; 54: e14355.  Back to cited text no. 4
    
5.
Bieniek JM, Lapin CD, Jarvi KA. Genetics of CFTR and male infertility. Transl Androl Urol 2021; 10: 1391–400.  Back to cited text no. 5
    
6.
Bieth E, Hamdi SM, Mieusset R. Genetics of the congenital absence of the vas deferens. Hum Genet 2021; 140: 59–76.  Back to cited text no. 6
    




 

 
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