Effect of one-year lumacaftor-ivacaftor treatment on glucose tolerance abnormalities in cystic fibrosis patients.

Bastien Misgault,Eva Chatron,Quitterie Reynaud,Sandrine Touzet,Michel Abely, Laurent Melly,Stéphane Dominique,Françoise Troussier, Olivia Ronsin-Pradel,Michèle Gerardin,Julie Mankikian, Laure Cosson, Raphael Chiron, Leila Bounyar, Michel Porzio,Isabelle Durieu,Laurence Weiss,Romain Kessler,Laurence Kessler

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society(2020)

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摘要
OBJECTIVES:To investigate the effects of 1-year lumacaftor-ivacaftor treatment on abnormalities in glucose tolerance (AGT) in Phe508del homozygous cystic fibrosis (CF) patients. METHODS:Untreated CF patients with glucose intolerance or newly diagnosed diabetes were included in a prospective, observational study. After 1-year lumacaftor-ivacaftor treatment, AGT were evaluated by using oral glucose tolerance test. RESULTS:Forty patients participated. 78% of patients had glucose intolerance and 22% diabetes at baseline. After one-year treatment, 50% of patients had normal glucose tolerance, 40% glucose intolerance, and 10% diabetes (p <0.001). The two-hour OGTT glycemia decreased from 171 (153-197) to 139 (117-162) mg/dL (p <0.001). 57.5% (n = 23) of patients improved their glucose tolerance with a significant decrease in both 1-hour (p<0.01) and 2-hour (p<0.001) OGTT glycemia. CONCLUSION:Improvements in AGT were observed following 1-year lumacaftor-ivacaftor treatment. Larger studies are needed to comprehensively assess CF transmembrane conductance regulator (CFTR) modulators.
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