Evidence map›Paper›PMID 41889676›Full record

ArticlePragmatic and observational research2026

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.

Bernardino Alcázar-Navarrete, Heath Heatley, Alan Kaplan, Lee Tze Tan, Mariko Siyue Koh, Naveed Sattar, John Townend, Derek Skinner, Victoria Carter, David Price

Abstract read
In one paragraph

Article in Pragmatic and observational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Bernardino Alcázar-NavarreteProfessor at Department of Medicine. Respiratory Department. Hospital Universitario Virgen de Las Nieves. Ibs, Granada, University of Granada, Granada, Spain.ORCID 0000-0003-2356-9366
Heath HeatleyObservational and Pragmatic Research Institute, Singapore, Singapore.ORCID 0009-0006-8500-1812
Alan KaplanFamily Physician Airways Group of Canada, Stouffville, Ontario, Canada.ORCID 0000-0001-8795-5528
Lee Tze TanNational University Health System, Department of Family Medicine, Singapore, Singapore.ORCID 0000-0001-6487-5672
Mariko Siyue KohDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0002-1230-0129
Naveed SattarProfessor of Cardiometabolic Medicine at the School of Cardiovascular & Metabolic Health at the University of Glasgow, Glasgow, UK.ORCID 0000-0002-1604-2593
John TownendObservational and Pragmatic Research Institute, Singapore, Singapore.
Derek SkinnerObservational and Pragmatic Research Institute, Singapore, Singapore.ORCID 0000-0002-7112-9317
Victoria CarterObservational and Pragmatic Research Institute, Singapore, Singapore.ORCID 0000-0002-0333-3308
David PriceObservational and Pragmatic Research Institute, Singapore, Singapore.ORCID 0000-0002-9728-9992

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

COPDCOPD outcomesGLP-1 RAobesity

Identifiers

PMID41889676
PMCPMC13015956

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.