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非布司他对中重度肾功能损害痛风患者肾功能的影响。

Impact of Febuxostat on Renal Function in Gout Patients With Moderate-to-Severe Renal Impairment.

机构信息

Birmingham VA Medical Center, Birmingham, Alabama, and University of Alabama at Birmingham.

Johns Hopkins University, Baltimore, Maryland.

出版信息

Arthritis Rheumatol. 2016 Aug;68(8):2035-43. doi: 10.1002/art.39654.

Abstract

OBJECTIVE

Renal impairment is a risk factor for gout and a barrier to optimal gout management. We undertook this exploratory study to obtain data that have been heretofore limited regarding the safety and efficacy of febuxostat in patients with moderate-to-severe renal impairment (estimated glomerular filtration rate [GFR] 15-50 ml/minute/1.73 m(2) ).

METHODS

Ninety-six gout patients with moderate-to-severe renal impairment were enrolled in a 12-month multicenter, randomized, double-blind, placebo-controlled study. Patients were randomly assigned at a 1:1:1 ratio to receive 30 mg febuxostat twice daily, 40/80 mg febuxostat once daily, or placebo. The primary efficacy end point was the change in serum creatinine (Cr) level from baseline to month 12. Secondary end points included the change in estimated GFR from baseline to month 12 and the proportion of patients with a serum uric acid (UA) level of <6.0 mg/dl at month 12.

RESULTS

At month 12, there were no significant differences in the change in serum Cr level from baseline, or in the change in estimated GFR from baseline, in either febuxostat group compared to the placebo group. The proportion of patients with a serum UA level of <6.0 mg/dl at month 12 was significantly greater in both febuxostat groups compared to the placebo group (both P < 0.001). At least 1 treatment-emergent adverse event (TEAE) occurred in 78.1% of patients receiving 30 mg febuxostat twice daily, 87.5% of patients receiving 40/80 mg febuxostat once daily, and 78.1% of patients receiving placebo. TEAEs most frequently involved the categories of renal failure and impairment and renal function analyses.

CONCLUSION

Febuxostat proved to be efficacious in serum UA reduction and was well tolerated in gout patients with moderate-to-severe renal impairment. Patients randomly assigned to receive febuxostat demonstrated significantly lower serum UA levels and no significant deterioration in renal function.

摘要

目的

肾功能损害是痛风的一个危险因素,也是痛风管理优化的一个障碍。我们进行了这项探索性研究,以获得迄今为止有限的关于中重度肾功能损害(估计肾小球滤过率[GFR] 15-50ml/min/1.73m²)患者使用非布司他的安全性和疗效的数据。

方法

96 例中重度肾功能损害的痛风患者参与了一项为期 12 个月的多中心、随机、双盲、安慰剂对照研究。患者以 1:1:1 的比例随机分配接受非布司他 30mg 每日两次、非布司他 40/80mg 每日一次或安慰剂治疗。主要疗效终点是从基线到第 12 个月时血清肌酐(Cr)水平的变化。次要终点包括从基线到第 12 个月时估计肾小球滤过率的变化,以及第 12 个月时血尿酸(UA)水平<6.0mg/dl 的患者比例。

结果

在第 12 个月时,与安慰剂组相比,两个非布司他组的血清 Cr 水平从基线的变化或估计 GFR 从基线的变化均无显著差异。与安慰剂组相比,两个非布司他组在第 12 个月时血尿酸水平<6.0mg/dl 的患者比例均显著更高(均 P<0.001)。接受 30mg 非布司他每日两次治疗的患者中有 78.1%、接受 40/80mg 非布司他每日一次治疗的患者中有 87.5%和接受安慰剂治疗的患者中有 78.1%至少发生了 1 次治疗中出现的不良事件(TEAE)。TEAEs 最常涉及肾衰竭和损伤以及肾功能分析类别。

结论

非布司他在降低血尿酸方面证明是有效的,在中重度肾功能损害的痛风患者中耐受性良好。随机接受非布司他治疗的患者血清 UA 水平显著降低,肾功能无明显恶化。

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