Febuxostat may decrease the incidence of COVID-19 infection among patients with gout: a retrospective cohort study

非布索坦 医学 痛风 别嘌呤醇 高尿酸血症 回顾性队列研究 内科学 入射(几何) 危险系数 尿酸 队列研究 肾功能 累积发病率 苯溴马隆 倾向得分匹配 托弗斯 队列 置信区间 风险因素 外科 相对风险 比例危险模型 低风险 不利影响 优势比 肾脏疾病 子群分析
作者
Weijie Wang,Shiow-Ing Wang,Yang Cheng,Xinchang Wang,Yongsheng Fan,James Cheng-Chung Wei,Weijie Wang,Shiow-Ing Wang,Yang Cheng,Xinchang Wang,Yongsheng Fan,James Cheng-Chung Wei
出处
期刊:Frontiers in Pharmacology [Frontiers Media]
卷期号:16
标识
DOI:10.3389/fphar.2025.1654173
摘要

Background As COVID-19 infection causes a kidney proximal tubule dysfunction with urinary loss of uric acid. Hypouricemia has been found in patients with severe COVID-19 disease. However, gout is a risk factor for COVID-19 incidence and COVID-19-related death. It is not known whether urate-lowering therapy could reduce the risk of infection of COVID-19 in gout patients or not. Methods Data from collaborative electronic health records were used in this study. A total of 663,729 patients with gout were enrolled between January 1, 2020 and December31, 2022 from 35,528,077 participants in US Collaborative Network with at least two visits. After exclusion and propensity score matching, 5,466 patients with Febuxostat and 5,466 patients with Allopurinol in the comparison group were selected. The hazard ratios (HRs) and 95% confidence intervals of COVID-19 incidence, and mechanical utilization were calculated between Febuxostat and Allopurinol groups. Subgroup analyses on sex, age, levels of serum uric acid, with vaccination group and sensitivity analyses for gout patients due to renal impairment or with tophus, different follow-up durations and considered competing risk were performed. Results Compared to Allopurinol group, Febuxostat significantly reduced the risk of COVID-19 incidence (HR = 0.878 [0.801–0.963]) and hospitalization (HR = 0.874 [0.772–0.989]). Febuxostat appears to be more effective in male, elder, without record of COVID-19 vaccination, and gout patients with serum uric acid<10 mg/dL in reducing the risk of COVID-19 infection. In addition, Febuxostat markedly reduced the hospitalization (HR = 0.652 [0.485–0.877]) in gout patients due to renal impairment or with tophus and the risks of COVID-19 incidence (HR = 0.878 [0.801–0.963]). Conclusion In this retrospective cohort study, Febuxostat use was associated with a lower risk of COVID-19 among patients with gout for 3 years follow-up, even with renal impairment or tophus.
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