Cardiovascular safety associated with febuxostat versus allopurinol among patients with gout: Update with accumulated use of febuxostat.

Semin Arthritis Rheum

Division of Rheumatology Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea; Division of Rheumatology Department of Internal Medicine, Seoul National University College of Medicine, Seongnam, Korea. Electronic address:

Published: October 2022

AI Article Synopsis

  • A study was conducted to compare the cardiovascular safety of febuxostat and allopurinol in gout patients using a large Korean health database from 2011-2019.
  • The findings indicated that febuxostat users had a slightly lower incidence of major cardiovascular events compared to allopurinol users, with similar risks for most outcomes except for a significant reduction in all-cause mortality for those on febuxostat.
  • Overall, the research concluded that febuxostat has non-inferior cardiovascular safety and is associated with a 16% lower risk of death compared to allopurinol.

Article Abstract

Background: To re-evaluate comparative cardiovascular (CV) safety of febuxostat versus allopurinol among patients with gout following recent accumulated use of febuxostat.

Methods: Using 2011-2019 Korea National Health Insurance database, we conducted a cohort study comparing gout patients initiating febuxostat versus allopurinol, 1:1 matched on a propensity-score (PS) for >60 covariates. The primary outcome was a composite endpoint of myocardial infarction, coronary revascularization, and stroke. Secondary outcomes were individual components of the primary outcome, hospitalized heart failure, and all-cause mortality. Subgroup analyses were done for those at high CV risk, long-term users (follow-up >3 years), and those without chronic kidney disease. We used Cox proportional hazard models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs).

Results: We included 160,930 PS-matched pairs of febuxostat and allopurinol users (mean age 59.3 years, 79.6% male). Incidence rates of the primary outcome were 2.06 and 2.27 per 100 person-years for febuxostat and allopurinol users, respectively, with a HR [95% CI] of 1.03 [0.95-1.12] comparing febuxostat versus allopurinol initiators. We also observed similar risks for secondary outcomes, except for reduced all-cause mortality among febuxostat users (HR [95% CI] of 0.84 [0.78-0.91]). Subgroup analyses also showed non-inferior CV safety of febuxostat.

Conclusion: In this population-based cohort study including the largest number of febuxostat users to date, we found non-inferior CV safety of febuxostat versus allopurinol. There was a 16% reduction in all-cause mortality among febuxostat users.

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http://dx.doi.org/10.1016/j.semarthrit.2022.152080DOI Listing

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