In the semaglutide new-user cohort (n = 22,537), semaglutide initiation was associated with fewer airway exacerbations compared with sulfonylureas (weighted hazard ratio [wHR], 0.76; 95% CI, 0.60-0.96).1 The association was stronger at higher doses, with a wHR of 0.75 (95% CI, 0.58-0.95) at low doses and 0.28 (95% CI, 0.08-1.01) at medium or high doses, and was more pronounced in asthma (wHR, 0.20; 95% CI, 0.05-0.78) than in COPD (wHR, 0.76; 95% CI, 0.58-1.00).1
Were effects more asthma-specific and drug-specific?
No significant associations with airway exacerbations were observed for liraglutide, dulaglutide, or exenatide, regardless of dose or underlying lung disease, despite similarly sized new-user cohorts for each individual agent.1 Investigators said only semaglutide showed a significant reduction in airway exacerbations, with evidence of a dose-response relationship and an association substantially stronger in asthma than in COPD.1
Key Facts
Does semaglutide reduce asthma attacks?
In a real-world UK electronic health record study, semaglutide initiation was associated with a weighted hazard ratio of 0.20 for exacerbations in patients with asthma, corresponding to a nearly 40% reduction, compared with sulfonylureas.
Do other GLP-1 receptor agonists reduce airway exacerbations?
No. Liraglutide, dulaglutide, and exenatide showed no significant association with airway exacerbations, regardless of dose or underlying lung disease.
Should patients with asthma or COPD start a GLP-1 receptor agonist for their lung condition?
No. The study's lead investigator cautioned people with asthma or COPD against starting GLP-1 receptor agonists specifically for their lung condition outside current prescribing guidance, noting the findings need confirmation in clinical trials.
Each GLP-1 receptor agonist cohort included between roughly 20,000 and 22,000 new users compared against sulfonylurea initiators, and investigators applied the same weighting methodology across all 4 comparisons.1 Investigators said the differential findings across agents highlight the value of studying individual GLP-1 receptor agonists separately rather than as a single drug class, and asthma comorbidity may help guide GLP-1 receptor agonist selection in patients managed for diabetes and obesity.1
“This is one of the largest real-world studies to investigate GLP-1 receptor agonists and airways disease, and one of the first to examine whether effects differ between individual GLP-1 receptor agonists,” said Alexander Mathioudakis, MD, PhD, chair of the European Respiratory Society Group on Airway Pharmacology and Treatment and senior lecturer in respiratory medicine at the University of Manchester, who was not involved in the research.2 “It highlights the need to consider metabolic health as part of respiratory care.”
Bloom cautioned the findings should not change treatment decisions on their own, noting people with asthma or COPD should not start GLP-1 receptor agonists specifically for their lung condition outside current prescribing guidance.2 Investigators described the analysis as one of the largest real-world studies of GLP-1 receptor agonists and airways disease, and said the results support including respiratory outcomes, such as asthma attacks and COPD exacerbations, in future trials of metabolic therapies.2
References
Lee B, Cahill K, Bloom C. The differential effects of GLP-1 based therapies in airways disease. Presented at: European Respiratory Society (ERS) Congress 2026; September 5-9, 2026; Barcelona, Spain.