Journal of Investigative Medicine High Impact Case Reports · 2019 · 24 citations · 10 references
MedicineEndocrinologyPediatricsMetabolic RegulationPediatric Clinical PharmacologyPediatric EndocrinologyCystic FibrosisCystic Fibrosis PharmacotherapyDiabetes ManagementDiabetes MellitusGlycemic ControlInsulin TherapyCftr Gene MutationsCystic Fibrosis-associated Pancreatic InsufficiencyCystic Fibrosis-related DiabetesCystic Fibrosis-related Pancreatic DiseaseImpaired Insulin SensitivityIvacaftor TherapyPancreatic Endocrine InsufficiencyPediatric Cystic Fibrosis Pharmacotherapy
Cystic fibrosis-related diabetes (CFRD) is a common comorbidity in cystic fibrosis with pancreatic insufficiency occurring early in the disease process. Current treatment is exogenous insulin therapy as CFRD is due to impaired insulin secretion. Recent small studies have shown improvement in endogenous insulin secretion with a short period of ivacaftor therapy in primarily pediatric patients with cystic fibrosis transmembrane conductance regulator mutations amenable to potentiation. In this article, we present the case of an adult patient with long-standing CFRD who developed sustained improvement in glycemic control after initiation of ivacaftor.
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Clinical Care Guidelines for Cystic Fibrosis–Related Diabetes
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