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COPD flare-ups: two comparisons favored GLP-1, the third was a tie

Against an older drug class, GLP-1 use came with fewer exacerbations. Against SGLT2 inhibitors the hazard ratio was 0.94, with an interval reaching 1.00.

Dana Sullivan5 min read
Exacerbations per 100 person-yearsGLP-19.89DPP-411.49SGLT29.26DPP-411.4SGLT29.47GLP-110The third pair is the head-to-head, and it is nearly a tie.

Chronic obstructive pulmonary disease and type 2 diabetes travel together often enough that the same person is frequently offered a drug for each, and a comparative effectiveness study set out to ask which glucose-lowering drug leaves that person in hospital less often. It emulated three target trials in US insurance claims, matching patients aged 40 and over with both conditions [1]. The result is genuinely interesting, and the part most likely to be quoted is not the part that matters — the same problem we keep finding in the claims sellers make about this class.

Two comparisons that favor the newer drugs

Against DPP-4 inhibitors, GLP-1 receptor agonists came in at 9.89 moderate or severe exacerbations per 100 person-years against 11.49, a hazard ratio of 0.86 (95% CI 0.81 to 0.91) across 32,107 matched pairs. SGLT2 inhibitors against the same comparator ran 9.26 against 11.4, a hazard ratio of 0.81 (95% CI 0.76 to 0.86) across 27,991 pairs. Both hold up across the sensitivity and subgroup analyses the authors report.

And one that finds almost nothing

The third comparison put the two newer classes against each other, in 36,218 matched pairs, and the difference nearly vanished: 9.47 against 10.00 per 100 person-years, a hazard ratio of 0.94 with a 95% confidence interval of 0.89 to 1.00. The upper bound touches no effect. The rate difference tells the same story, at −0.55 per 100 person-years with an interval running to −0.01.

So the honest summary is that both beat an older class and neither clearly beats the other. Quoting only the first two comparisons would imply a ranking this study does not support, which is the shape of argument we have taken apart before where two meta-analyses of the same six trials disagreed.

Who was in it

The cohorts were old and sick by the standards of this market: a mean age near 70, type 2 diabetes, and COPD active enough to be coded as such. Median follow-up was 145 days, with an interquartile range of 61 to 355 — short, for a chronic lung condition. A person buying compounded semaglutide from a telehealth page at 45 with no lung disease is outside the population these numbers describe, and nothing here is a reason to choose a seller. It is a reason to make sure whoever writes the prescription knows the rest of your history, which is the gap we count in what sellers do not publish and put into questions they leave open.

Frequently asked

Do GLP-1 drugs reduce COPD flare-ups?
Against DPP-4 inhibitors, yes — 9.89 against 11.49 per 100 person-years, a hazard ratio of 0.86. Against SGLT2 inhibitors the difference was 0.94 with an interval reaching 1.00, which is close to nothing.
Does this apply to me if I do not have diabetes?
No. Every cohort required type 2 diabetes and active COPD, at a mean age near 70. That is not the population buying these drugs from a telehealth page.
How long were people followed?
A median of 145 days, with an interquartile range of 61 to 355 — short for a chronic lung condition.

Sources

  1. [1] Ray A, et al. (2025). Glucose-Lowering Medications and Risk of Chronic Obstructive Pulmonary Disease Exacerbations in Patients With Type 2 Diabetes JAMA Internal Medicine. PMID 39928303

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