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DOI 10.1016/j.jcf.2023.10.022

Медицинская библиотека · Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023

A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy.

Taylor-Cousar Jennifer L, Janney Rachel, Middleton Peter G, Jain Raksha, Nightingale Julia, West Natalie E, Shteinberg Michal, Velez Danielle, Kazmerski Traci M

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Most males with cystic fibrosis (mwCF) are infertile but with CF transmembrane conductance regulator (CFTR) modulator-conferred benefits, more are utilizing assisted reproductive technologies (ART). Administration of normal human doses of modulators in animal reproductive models caused no genotoxicity; no human data exists. Potential health decline following modulator discontinuation makes the decision to withhold therapy during reproduction challenging.

METHODS

From August-October 2021, international CF clinicians completed an anonymous questionnaire regarding mwCF who used modulators during reproduction.

RESULTS

We received 42 surveys for mwCF with partner pregnancies. Forty of 42 mwCF utilized ART; 35 continued modulators during sperm retrieval and 40/42 during partner pregnancy. One of four males who discontinued modulators experienced clinical deterioration. First trimester miscarriages occurred in 11.9 % of partner pregnancies. No congenital anomalies were reported.

CONCLUSIONS

Use of CFTR modulators during reproduction and partner pregnancy in mwCF did not result in a higher-than-expected miscarriage rate nor congenital anomalies.

Для цитирования: Taylor-Cousar Jennifer L, Janney Rachel, Middleton Peter G, Jain Raksha, Nightingale Julia, West Natalie E, Shteinberg Michal, Velez Danielle, Kazmerski Traci M. A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy.. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 2023. DOI: 10.1016/j.jcf.2023.10.022.

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