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NEJM Evidence· 2026Q1

Metoprolol in Chronic Obstructive Pulmonary Disease without Cardiovascular Disease

Josefin Sundh, Anders Magnuson, Marika Kvarnström, F. Sjöberg et al.

Short summary

In patients with COPD but no cardiovascular disease, metoprolol did not significantly reduce the time to a composite of COPD exacerbations, cardiovascular events, or death over 1 year (HR, 0.87; P=0.14).

AI-generated from the title and abstract; the full text is not read.

Key points

  • Metoprolol did not significantly reduce the primary composite endpoint (COPD exacerbation, cardiovascular event, or death) in COPD patients without cardiovascular disease (HR, 0.87; P=0.14).
  • The composite endpoint occurred in 27% of patients receiving metoprolol vs. 30% receiving standard care over 1 year.
  • Metoprolol showed a non-significant trend toward reducing cardiovascular events (HR, 0.73) but did not significantly impact COPD exacerbations or death.
  • Nonserious adverse events were more frequent in the metoprolol group (34.6%) compared to the standard care group (29.2%).

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND: Beta-blockers may improve outcomes in patients with chronic obstructive pulmonary disease (COPD) without cardiovascular disease, but randomized trials have been inconclusive. METHODS: This was a multicenter, open-label, pragmatic, phase 4 randomized trial. Patients 40 years of age or older with COPD, sinus rhythm, and no cardiovascular disease were randomly assigned in a 1:1 ratio to receive metoprolol, at a target dose of 100 mg daily, in addition to standard care or to receive standard care alone. The primary end point was the time to the first occurrence of a COPD exacerbation, cardiovascular event, or death during 1 year of follow-up. RESULTS: A total of 1695 patients underwent random assignment; their mean age was 70 years, and 62% were female. The primary end point occurred in 27% of patients assigned to receive metoprolol and in 30% assigned to receive standard care (hazard ratio, 0.87; 95% confidence interval [CI], 0.73 to 1.05; P=0.14). The corresponding hazard ratios were 0.88 (95% CI, 0.72 to 1.06) for COPD exacerbations, 0.73 (95% CI, 0.48 to 1.11) for cardiovascular events, 0.92 (95% CI, 0.48 to 1.77) for death, and 0.87 (95% CI, 0.58 to 1.28) for exacerbations requiring hospitalization. Serious adverse events occurred in 80 (9.4%) of 848 participants in the metoprolol group and 66 (7.8%) of 847 participants in the standard care group. Nonserious adverse events occurred in 293 (34.6%) of 848 patients in the metoprolol group and 247 (29.2%) of 847 in the standard care group. CONCLUSIONS: Among patients with COPD and no cardiovascular disease, metoprolol did not significantly improve the time to a composite of exacerbations, cardiovascular events, or death. (Funded by research grants from the Swedish Research Council and others; ClinicalTrials.gov number, NCT03566667.).

The authors' abstract, as published at the source. NEJM Evidence, 2026 · DOI ↗

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Field: Pulmonary and Respiratory Medicine

Pulmonary and Respiratory MedicineMedicine