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
Case Reports
. 2022 Feb 21:13:773753.
doi: 10.3389/fendo.2022.773753. eCollection 2022.

The Prognosis of ART Is Not Altered in Cystic Fibrosis Women: A Case-Report Study

Affiliations
Case Reports

The Prognosis of ART Is Not Altered in Cystic Fibrosis Women: A Case-Report Study

Inès Braham et al. Front Endocrinol (Lausanne). .

Abstract

Research question: Unlike in men, a very limited number of studies were focused on the specificity of ART management of cystic fibrosis (CF) in women. The purpose of this study was to determine the causes of infertility in patients, the appropriate ART treatment, and their prognosis in terms of pregnancy.

Design: We conducted a multicentre analytical case-control study including CF women who were age-matched to non-CF women. We reported the causes of infertility, the ART management type and pregnancy outcomes.

Results: 17 cases were compared to 34 controls. There was no significant difference between the groups concerning cause infertility. There was a non-statistically significant trend with a lower antral follicle count in CF compared to controls (19.5 versus 26.8, p=0.08). IUI seemed to be as successful as IVF/ICSI in CF as opposed to controls where the IVF/ICSI was the most effective (in CF group for HCG >100 UI/L: 38.8% vs. 36.8%, p=0.4175). There were more embryos obtained in CF than in controls (3.1 versus 1.6, p=0.02). The number of oocytes and embryos obtained and pregnancy outcomes remained similar between DF508 homozygous group and others CFTR mutations group. The results of ART procedures and pregnancy evolution were not influenced by FEV1.

Conclusion: In absence of any other pathology, IUI may be first option for CF women. If insemination fails, IVF with a low dose of gonadotropins may be more appropriate to prevent the risk of hyperstimulation syndrome. FEV1 and genetic do not seem to be contributing factors in the prognosis of ART.

Keywords: assisted reproductive techniques; cystic fibrosis; female; infertility; pregnancy; pregnancy outcome.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

    1. Scotet V, Duguépéroux I, Saliou P, Rault G, Roussey M, Audrézet M-P, et al. . Evidence for Decline in the Incidence of Cystic Fibrosis: A 35-Year Observational Study in Brittany, France. Orphanet J Rare Dis (2012) 7(1):14. doi: 10.1186/1750-1172-7-14 - DOI - PMC - PubMed
    1. Elborn JS. Cystic Fibrosis. Lancet (2016) 388(10059):2519–31. doi: 10.1016/S0140-6736(16)00576-6 - DOI - PubMed
    1. Ramsey BW, Davies J, Gerard McElvaney N, Tullis E, Bell SC, Dřevínek P, et al. . A CFTR Potentiator in Patients With Cystic Fibrosis and the G551D Mutation. N Engl J Med (2011) 365(18):1663–72. doi: 10.1056/NEJMoa1105185 - DOI - PMC - PubMed
    1. Heijerman HGM, McKone EF, Downey DG, Braeckel EV, Rowe SM, Tullis E, et al. . Efficacy and Safety of the Elexacaftor Plus Tezacaftor Plus Ivacaftor Combination Regimen in People With Cystic Fibrosis Homozygous for the F508del Mutation: A Double-Blind, Randomised, Phase 3 Trial. Lancet (2019) 394(10212):1940–8. doi: 10.1016/S0140-6736(19)32597-8 - DOI - PMC - PubMed
    1. Scotet V, L’Hostis C, Férec C. The Changing Epidemiology of Cystic Fibrosis: Incidence, Survival and Impact of the CFTR Gene Discovery. Genes (2020) 11(6):E589. doi: 10.3390/genes11060589 - DOI - PMC - PubMed

Publication types