Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Sep 5;10(17):4009.
doi: 10.3390/jcm10174009.

Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients' and Offspring Health

Affiliations
Review

Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients' and Offspring Health

Csilla Krausz et al. J Clin Med. .

Abstract

Non-Obstructive Azoospermia (NOA) affects about 1% of men in the general population and is characterized by clinical heterogeneity implying the involvement of several different acquired and genetic factors. NOA men are at higher risk to be carriers of known genetic anomalies such as karyotype abnormalities and Y-chromosome microdeletions in respect to oligo-normozoospermic men. In recent years, a growing number of novel monogenic causes have been identified through Whole Exome Sequencing (WES). Genetic testing is useful for diagnostic and pre-TESE prognostic purposes as well as for its potential relevance for general health. Several epidemiological observations show a link between azoospermia and higher morbidity and mortality rate, suggesting a common etiology for NOA and some chronic diseases, including cancer. Since on average 50% of NOA patients has a positive TESE outcome, the identification of genetic factors in NOA patients has relevance also to the offspring's health. Although still debated, the observed increased risk of certain neurodevelopmental disorders, as well as impaired cardiometabolic and reproductive health profile in children conceived with ICSI from NOA fathers may indicate the involvement of transmissible genetic factors. This review provides an update on the reproductive and general health consequences of known genetic factors causing NOA, including offspring's health.

Keywords: ICSI; NOA; WES; Y chromosome; azoospermia; cancer; exome; general health; genes; genetics; infertility; offspring health.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Clinical relevance of genetic testing in azoospermic men.

References

    1. Tournaye H., Krausz C., Oates R.D. Novel concepts in the aetiology of male reproductive impairment. Lancet Diabetes Endocrinol. 2017;5:544–553. doi: 10.1016/S2213-8587(16)30040-7. - DOI - PubMed
    1. Krausz C., Riera-Escamilla A. Genetics of male infertility. Nat. Rev. Urol. 2018;15:369–384. doi: 10.1038/s41585-018-0003-3. - DOI - PubMed
    1. Cioppi F., Rosta V., Krausz C. Genetics of Azoospermia. Int. J. Mol. Sci. 2021;22:3264. doi: 10.3390/ijms22063264. - DOI - PMC - PubMed
    1. Kasak L., Laan M. Monogenic causes of non-obstructive azoospermia: Challenges, established knowledge, limitations and perspectives. Hum. Genet. 2021;140:135–154. doi: 10.1007/s00439-020-02112-y. - DOI - PubMed
    1. Capalbo A., Poli M., Riera-Escamilla A., Shukla V., Høffding M.K., Krausz C., Hoffmann E.R., Simon C. Preconception genome medicine: Current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data. Hum. Reprod. Update. 2021;27:254–279. doi: 10.1093/humupd/dmaa044. - DOI - PubMed

LinkOut - more resources