The Potential Impact of GLP-1 Receptor Agonists on Exacerbation Risk in Patients with COPD and Type 2 Diabetes: A Real-World Population-Based Observational Study
Metadatos
Mostrar el registro completo del ítemAutor
Alcázar Navarrete, Bernardino; Heatley, Heath; Kaplan, Alan; Tze Tan, Lee; Siyue Koh, Mariko; Sattar, Naveed; Townend, John; Skinner, Derek; Carter, Victoria; Price, DavidEditorial
Taylor & Francis
Materia
COPD Obesity COPD outcomes
Fecha
2026-01-30Referencia bibliográfica
Alcázar-Navarrete, B., Heatley, H., Kaplan, A., Tan, L., Koh, M., Sattar, N., Townend, J., Skinner, D., Carter, V., & Price, D. (2026). The potential impact of GLP-1 receptor agonists on exacerbation risk in patients with COPD and type 2 diabetes: A real-world population-based observational study. Pragmatic and Observational Research, 17, 1–10. https://doi.org/10.2147/por.s550543
Resumen
Introduction: There is limited evidence on the impact of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in patients with
chronic obstructive pulmonary disease (COPD).
Material and Methods: We conducted a retrospective matched cohort study including patients aged ≥40 years with COPD and T2D.
Patients initiating GLP-1 RAs were matched 1:1 with GLP-1 naïve controls based on age, sex, smoking status, COPD treatment
(LABA/LAMA/ICS), and exacerbation history. The index date was defined as the first GLP-1 RA prescription, control’s index date
was a COPD consultation within 186 days of matched patient index. The primary outcome was the number of COPD exacerbations
during the 12 months following the index date. Secondary outcomes included oral corticosteroid (OCS) prescriptions and hospital
resource utilization (HCRU). Poisson regression models adjusted for BMI and other confounders were used to estimate incidence rate
ratios (IRR).
Results: A total of 4479 matched patients were included. There were no significant differences between groups in exacerbation rates
or OCS use in the year prior to the index date. During follow-up, patients treated with GLP-1 RAs had significantly fewer
exacerbations (adjusted IRR [aIRR] 0.84, 95% CI: 0.79–0.89) and fewer OCS prescriptions (aIRR 0.86, 95% CI: 0.77–0.95) compared
with controls. A significant delay in time to first OCS prescription was also observed.
Conclusion: In this real-world cohort, initiation of GLP-1 RA treatment in patients with COPD and T2D was associated with lower
COPD exacerbations and OCS use. These findings suggest a potential role for GLP-1 RAs in modifying the course of COPD in this
comorbid population, warranting randomised trials





