Exogenous insulin does not reduce protein catabolism in pre-diabetic cystic fibrosis patients: A randomized clinical trial.

Autor: Schiavon M; Department of Information Engineering, University of Padova, Via Gradenigo 6b, 35131, Padova, Italy. Electronic address: michele.schiavon@dei.unipd.it., Cobelli C; Department of Woman and Child's Health, University of Padova, Via Giustiniani n 3, 35128, Padova, Italy. Electronic address: cobelli@dei.unipd.it., Nair KS; Mayo Clinic College of Medicine, Division of Endocrinology and Research, 200 1st St SW, 5-194 Joseph, Rochester MN 55905. Electronic address: Nair@mayo.edu., Klaus K; Mayo Clinic College of Medicine, Division of Endocrinology and Research, 200 1st St SW, 5-194 Joseph, Rochester MN 55905. Electronic address: Klaus.Katherine@mayo.edu., Toffolo G; Department of Information Engineering, University of Padova, Via Gradenigo 6b, 35131, Padova, Italy. Electronic address: giannamaria.toffolo@unipd.it., Zhang L; Division of Biostatistics and Health Data Science, School of Public Health, University of Minnesota, University Office Plaza, Suite 200, 2221 University Avenue SE, Minneapolis, MN 55414. Electronic address: zhan4800@umn.edu., Moran A; Department of Pediatrics, University of Minnesota, Academic Office Building, AOB-120, 2450 Riverside Ave, Minneapolis, Minnesota 55454. Electronic address: moran001@umn.edu.
Jazyk: angličtina
Zdroj: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society [J Cyst Fibros] 2024 Nov 07. Date of Electronic Publication: 2024 Nov 07.
DOI: 10.1016/j.jcf.2024.10.005
Abstrakt: Background: Cystic Fibrosis (CF) patients historically suffered from undernutrition, infection and inflammation. Insulin insufficiency-related protein catabolism further compromised health. We aimed to determine whether insulin improves protein catabolism in CF youth with abnormal glucose tolerance (AGT).
Methods: This double-masked, placebo-controlled trial in CF youth age 10-25 with AGT who were in their usual state of health used triple-tracer stable-isotope methodology to measure protein turnover during a baseline test meal and after four weeks of insulin/placebo treatment. Healthy controls were assessed once. CF patients were randomized 1:1:1 to once-daily long-acting insulin (0.25 U/kg/d), three-times daily rapid-acting insulin (0.5 U/15gr carbohydrate), or injectable placebo.
Results: Thirty CF patients completed the study. There were no differences in any measure of protein turnover between insulin- and placebo-treated subjects, including endogenous protein breakdown (primary study endpoint). In contrast to earlier studies, protein turnover in the 37 CF patients who completed the baseline meal was normal compared to 20 healthy controls. Meal isotope appeared in plasma earlier in CF than controls, suggesting more rapid gut emptying. The study was interrupted by the pandemic; futility analysis led to study discontinuation before the planned remaining 15 CF patients were studied.
Conclusions: Recent advances in CF have led to remarkable clinical improvements. In this study, CF youth with AGT had normal protein catabolism at baseline. Pre-meal or daily basal insulin therapy, while safe and well tolerated, did not significantly enhance protein turnover and does not appear to be necessary in clinically stable patients prior to development of CFRD.
Competing Interests: Declaration of competing interest Schiavon M: None, Cobelli C: None, Nair KS: None, Klaus K: None, Toffolo, G: None, Zhang L: None, Moran A: Over the last 5 years Dr. Moran reports serving on scientific advisory boards for Dompé Farmaceutici SpA, ProventionBio, Vertex Pharaceuticals and Abata Therapeutics; serving on data and safety monitoring boards funded by NovoNordisk and the Leona M. and Harry B. Helmsley Charitable Trust; her institution has received grant funding on her behalf from the NIH, JDRF, the Cystic Fibrosis Foundation, Abbott Diabetes, ProventionBio, Intrexon (now Precigen), and Caladrius Biosciences; she has received study supplies from Medtronic and Abbott Diabetes.
(Copyright © 2024. Published by Elsevier B.V.)
Databáze: MEDLINE
Externí odkaz: