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Abstract
Obesity and cardiometabolic dysfunction are increasingly recognized in people with cystic fibrosis (pwCF).
- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may influence lung function and respiratory outcomes in pwCF.
- The relationship between pulmonary improvement and metabolic response after starting GLP-1 RAs is not fully understood.
- Treatment intensity could be a factor in the pulmonary response to GLP-1 RAs in pwCF.
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