Hypoglycaemia after Initiation of CFTR Modulator Therapy in a Cystic Fibrosis Patient without Diabetes

Author:

Yskout Marie1,Vliebergh Joke1,Bor Hakan23,Dupont Lieven34ORCID,Lorent Natalie34ORCID,Van Bleyenbergh Pascal34,Gillard Pieter13ORCID,Van der Schueren Bart13ORCID,Mertens Ann13ORCID,Mathieu Chantal13ORCID,Vangoitsenhoven Roman13ORCID

Affiliation:

1. UZ Leuven, Endocrinology, Leuven, Belgium

2. Nutrition and Dietetic, Gumushane University, Gumushane, Türkiye

3. Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium

4. Pneumology, UZ Leuven, Leuven, Belgium

Abstract

Introduction. Cystic fibrosis transmembrane regulator (CFTR) modulator therapies improve respiratory function and glycaemic control in patients with cystic fibrosis (CF). The direct effect of CFTR modulator therapies on pancreatic function in patients without preexisting diabetes remains unclear. Case Presentation. An 18-year-old female with CF caused by F508del/F508del mutation, who had no diabetes, developed postprandial hypoglycaemias 6 months after initiation of elexacaftor, tezacaftor, and ivacaftor combination therapy (ETI). Symptoms were persisted after brief discontinuation of ETI, but her symptoms and time-in-hypoglycaemia had improved remarkably by avoiding high glycaemic index-foods. Discussion. This case of hypoglycaemia associated with CFTR modulator therapy in a patient without preexisting diabetes suggests that CFTR modulator therapy has the potential to directly affect glucose homeostasis. There might be an improvement in insulin secretion as well as a reduction in systemic insulin resistance. Conclusion. Treatment of CF patients without diabetes with CFTR modulator therapies can cause recurrent hypoglycaemic episodes which resolve with dietary measures.

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

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