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Atrial Fibrillation Risk and Urate-Lowering Therapy in Patients with Gout: A Cohort Study Using a Clinical Database
Ching-Han Liu1,2,3, Shih-Chung Huang1,2,4, Chun-Hao Yin5,6
1Division of Cardiology, Department of Medicine, Kaohsiung Armed Forces General Hospital, Kaohsiung 80284, Taiwan.
Insights
Asian individuals with gout treated with urate-lowering therapy (ULT) showed no increased risk of atrial fibrillation (AF) with febuxostat compared to allopurinol. This study investigated AF development after ULT in an Asian population.
Area of Science:
- Cardiology
- Rheumatology
- Pharmacology
Background:
- Asian populations have a higher predisposition to hyperuricemia and gout.
- Urate-lowering therapy (ULT) is crucial for managing gout.
- Previous studies suggested febuxostat may increase atrial fibrillation (AF) risk in elderly individuals, but this remains uninvestigated in Asian populations.
Purpose of the Study:
- To investigate the association between different ULTs (allopurinol, benzbromarone, febuxostat) and the incidence of AF in an Asian gout patient cohort.
- To compare the risk of developing AF among patients treated with febuxostat versus other ULTs.
Main Methods:
- A retrospective cohort study was conducted using a clinical database.
- Patients newly diagnosed with gout between 2013-2020 with baseline serum uric acid levels and no prior AF diagnosis were included.
- Patients were categorized into allopurinol, benzbromarone, or febuxostat user groups for comparative risk assessment of incident AF.
Main Results:
- Out of 713 eligible patients, 43 (6%) developed incident AF during a mean follow-up of 49.4 months.
- Febuxostat users exhibited higher rates of comorbidities like diabetes mellitus, heart failure, and chronic kidney disease, along with elevated CHA2DS2-VASc scores.
- Adjusted hazard ratios showed no significant increase in AF risk for febuxostat or benzbromarone compared to allopurinol (HR: 1.20, 95% CI: 0.43-3.34 and HR: 0.68, 95% CI: 0.22-2.08, respectively).
Conclusions:
- In this Asian cohort, no significant difference in the risk of incident AF was observed among patients with gout receiving febuxostat, allopurinol, or benzbromarone.
- The findings suggest that febuxostat does not elevate AF risk in Asian patients with gout compared to other common ULTs.
- Further long-term studies are warranted to comprehensively evaluate cardiovascular outcomes associated with different ULTs in diverse patient populations.
Abstract:
Individuals of Asian descent are at higher risk for developing hyperuricemia and gout as compared to Western populations. Urate-lowering therapy (ULT) is an effective treatment for hyperuricemia and gout. It was reported that febuxostat, one of the ULTs, raises the risk of atrial fibrillation (AF) in elderly populations. Nevertheless, this association has not been properly investigated in Asian populations. We aimed to investigate the development of AF after ULT with different drugs in an Asian population. We conducted a retrospective cohort study using the clinical database at Kaohsiung Veterans General Hospital. Patients newly diagnosed with gout between 1 January 2013 and 31 December 2020 and with a documented baseline serum uric acid (sUA) level but no prior diagnosis of AF were identified. Patients were divided into three groups-allopurinol, benzbromarone, and febuxostat users. During the follow-up period, the risks of incident AF following the initiation of ULT with different drugs were assessed. Development of incident AF was noted in 43 (6%) of the 713 eligible patients during the follow-up period (mean, 49.4 ± 26.6 months). Febuxostat-treated patients had a higher prevalence of certain comorbidities (diabetes mellitus, heart failure, and chronic kidney disease) and higher CHA2DS2-VASc scores. Compared with allopurinol, neither febuxostat nor benzbromarone was associated with increased adjusted hazard ratios (HR) for incident AF (HR: 1.20, 95% confidence interval [CI]: 0.43-3.34; HR: 0.68, 95% CI: 0.22-2.08). There was no difference in the risk of incident AF among Asian patients with gout who received febuxostat, allopurinol, or benzbromarone. Further studies are needed to evaluate long-term cardiovascular outcomes in patients receiving different ULT drugs.
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