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Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass

Background: Ivacaftor, the first CFTR modulator drug, leads to significant long-term improvement in lung function and weight gain. The mechanism as well as the long-term impact of ivacaftor on weight, resting energy expenditure (REE) and body composition remains to be explored. Methods: This prospec...

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Autores principales: Mouzaki, Marialena, Dupuis, Annie, Avolio, Julie, Griffin, Katherine, Ratjen, Felix, Tullis, Elizabeth, Gonska, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372433/
https://www.ncbi.nlm.nih.gov/pubmed/37521467
http://dx.doi.org/10.3389/fphar.2023.1157459
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author Mouzaki, Marialena
Dupuis, Annie
Avolio, Julie
Griffin, Katherine
Ratjen, Felix
Tullis, Elizabeth
Gonska, Tanja
author_facet Mouzaki, Marialena
Dupuis, Annie
Avolio, Julie
Griffin, Katherine
Ratjen, Felix
Tullis, Elizabeth
Gonska, Tanja
author_sort Mouzaki, Marialena
collection PubMed
description Background: Ivacaftor, the first CFTR modulator drug, leads to significant long-term improvement in lung function and weight gain. The mechanism as well as the long-term impact of ivacaftor on weight, resting energy expenditure (REE) and body composition remains to be explored. Methods: This prospective observational study included 18 people with CF (pwCF) (age: median (range) 20 (6–58) years) carrying at least one CFTR gating mutation commencing ivacaftor. Assessments of body composition, REE and laboratory investigations were performed at baseline and 6, 12 and 24 months after treatment initiation. Results: Treatment with ivacaftor was associated with a significantly positive change in BMI z-score at 24 months. Fat mass (mean (95% CL) of 6.5 kg (4.0; 9.0) from baseline, p = 0.0001), but not fat-free mass changed under ivacaftor treatment. There was a significant positive correlation between weight and fat mass change. Overall, there was no significant change in measured REE from baseline (mean (95% CL) of 108 kcal/d (−12; 228), p = 0.07) in our cohort. Pancreatic function and other nutritional markers did not change with treatment, with the exception of an increase in serum vitamin A levels (p = 0.006). Conclusion: The weight gain observed in ivacaftor treated pwCF is predominantly secondary to increases in fat mass warranting early counseling of people starting on CFTR-modulating treatment with respect to healthy diet and physical exercise.
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spelling pubmed-103724332023-07-28 Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass Mouzaki, Marialena Dupuis, Annie Avolio, Julie Griffin, Katherine Ratjen, Felix Tullis, Elizabeth Gonska, Tanja Front Pharmacol Pharmacology Background: Ivacaftor, the first CFTR modulator drug, leads to significant long-term improvement in lung function and weight gain. The mechanism as well as the long-term impact of ivacaftor on weight, resting energy expenditure (REE) and body composition remains to be explored. Methods: This prospective observational study included 18 people with CF (pwCF) (age: median (range) 20 (6–58) years) carrying at least one CFTR gating mutation commencing ivacaftor. Assessments of body composition, REE and laboratory investigations were performed at baseline and 6, 12 and 24 months after treatment initiation. Results: Treatment with ivacaftor was associated with a significantly positive change in BMI z-score at 24 months. Fat mass (mean (95% CL) of 6.5 kg (4.0; 9.0) from baseline, p = 0.0001), but not fat-free mass changed under ivacaftor treatment. There was a significant positive correlation between weight and fat mass change. Overall, there was no significant change in measured REE from baseline (mean (95% CL) of 108 kcal/d (−12; 228), p = 0.07) in our cohort. Pancreatic function and other nutritional markers did not change with treatment, with the exception of an increase in serum vitamin A levels (p = 0.006). Conclusion: The weight gain observed in ivacaftor treated pwCF is predominantly secondary to increases in fat mass warranting early counseling of people starting on CFTR-modulating treatment with respect to healthy diet and physical exercise. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10372433/ /pubmed/37521467 http://dx.doi.org/10.3389/fphar.2023.1157459 Text en Copyright © 2023 Mouzaki, Dupuis, Avolio, Griffin, Ratjen, Tullis and Gonska. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Mouzaki, Marialena
Dupuis, Annie
Avolio, Julie
Griffin, Katherine
Ratjen, Felix
Tullis, Elizabeth
Gonska, Tanja
Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title_full Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title_fullStr Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title_full_unstemmed Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title_short Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass
title_sort weight increase in people with cystic fibrosis on cftr modulator therapy is mainly due to increase in fat mass
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372433/
https://www.ncbi.nlm.nih.gov/pubmed/37521467
http://dx.doi.org/10.3389/fphar.2023.1157459
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