与别嘌呤醇相比,非布司他强化降尿酸治疗对痛风和心血管风险增加患者脉搏波速度的影响:FORWARD研究

Giovambattista Desideri, Marek Rajzer, Martijn Gerritsen, Michael T Nurmohamed, Cristina Giannattasio, Anne-Kathrin Tausche, Claudio Borghi
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引用次数: 8

摘要

目的:高尿酸血症和痛风与传统的心血管危险因素和血管损伤密切相关。本研究旨在评估非布司他和别嘌呤醇是否对痛风和血清尿酸(SUA)水平升高患者的颈-股脉波速度(cfPWV)有不同影响。方法和结果:一项多中心、多国、IV期、随机、平行组、主动对照、开放标签的盲终点评价试验。197名痛风且SUA水平≥8mg /dL的成年人按1:1的比例随机分配到非布司他或别嘌呤醇组,持续36周。主要结果是比较非布司他和别嘌呤醇对cfPWV变化的影响。随机分组和第36周时,非布司他组的平均cfPWV值分别为8.69和9.00 m/s,别嘌呤醇组的平均cfPWV值分别为9.02和9.05 m/s。在任何时间点,任何评估参数的cfPWV均未因治疗分配而发生统计学显著变化。更多接受非布司他治疗的受试者治疗后血清尿酸浓度≤6 mg/dL(第36周时78.3% vs. 61.1%, P = 0.0137)。51例(52.0%)患者随机分到非布司他组,63例(62.5%)患者随机分到别嘌呤醇组。两个治疗组的大多数事件都是轻微的,包括痛风发作和关节痛。结论:非布司他和别嘌呤醇均可使痛风合并SUA水平升高的患者动脉僵硬度保持稳定。非布司他比别嘌呤醇更有效、更快地达到SUA目标。两种治疗方法都是安全且耐受性良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of intensive urate lowering therapy with febuxostat in comparison with allopurinol on pulse wave velocity in patients with gout and increased cardiovascular risk: the FORWARD study.

Aims: Hyperuricaemia and gout are strongly related with traditional cardiovascular risk factors and vascular damage. This study aimed to assess whether febuxostat and allopurinol could differently influence carotid-femoral pulse wave velocity (cfPWV) in patients with gout and elevated serum uric acid (SUA) levels.

Methods and results: A multi-centre, multinational, phase IV, randomized, parallel-group, active-controlled, open-label trial with blind endpoints evaluation. One hundred and ninety-seven adults with gout and SUA levels ≥8 mg/dL were randomized to febuxostat or allopurinol in a 1:1 ratio for 36 weeks. The primary outcome was the comparison of the effects of febuxostat and allopurinol on changes in cfPWV. The mean cfPWV values at randomization and Week 36 were 8.69 and 9.00 m/s, respectively for subjects randomized to febuxostat and 9.02 and 9.05 m/s for subjects randomized to allopurinol. No statistically significant changes in cfPWV by treatment assignment were observed at any time point for any of the assessed parameters. More subjects who received febuxostat had serum urate concentrations ≤6 mg/dL following treatment (78.3% vs. 61.1% at Week 36, P = 0.0137). Treatment-emergent adverse events were reported by 51 (52.0%) patients randomized to febuxostat and 63 (62.5%) patients randomized to allopurinol. The majority of events were mild in both treatment groups and included gout flares and arthralgia.

Conclusion: In patients with gout and elevated SUA levels the arterial stiffness remained stable both with febuxostat and allopurinol. Febuxostat was more effective and faster than allopurinol in achieving the SUA target. Both treatments were safe and well tolerated.

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