Febuxostat efficacy in patients with gout depending on kidney function

M. Eliseev, O. Zhelyabina, M. Chikina, M.M. Thakokov
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引用次数: 2

Abstract

Aim: to determine the probability of achieving the target serum uric acid (UA) level during therapy with febuxostat (in the tablet form) in patients with gout stratified depending on kidney function, including patients with type 2 diabetes mellitus (DM2). Patients and Methods: the study included patients over 18 years of age with gout who had not previously taken febuxostat or other urate- lowering drugs for at least 2 weeks before inclusion, with a serum UA level >360 μmoL/L. All were prescribed with febuxostat in the tablet form 80 mg/day. If the target serum UA level was not reached (<360 μmoL/L), the dosage level was increased up to 120 mg/day. Laboratory tests included the determination of blood glucose, creatinine, UA. Initially, patients were divided into groups according to chronic kidney disease (CKD) stages by the level of estimated glomerular filtration rate (eGFR) by CKD-EPI: C1 — high or optimal renal function (>90 mL/min/1.73 m2), C2 — slightly reduced renal function (60–89 mL/min/1.73 m2), C3 — moderately/considerably reduced renal function (30–59 mL/ min/1.73 m2), C4 — significantly reduced renal function (15–29 mL/min/1.73 m2). Patients with DM2 were analyzed separately. The follow-up period covered at least 26 weeks: the primary endpoint was to achieve the target serum UA level, and the eGFR tendency was also evaluated.Results: 136 patients with gout were examined. DM2 was in 38 (27.9%) patients. CKD C0–1 was detected in 30 (22.1%) patients, C2 — in 28 (20.6%), C3 — in 62 (45.6%), C4 — in 16 (11.8%). Febuxostat (in the tablet form) was received at a dose of 80 mg/day in 98 (72.1%) patients, 120 mg/day in 38 (27.9%) patients. There was the following preventive administration of anti-inflammatory therapy: colchicine — 59 (43.4%) patients, NSAIDs — 51 (37.5%) patients, glucocorticosteroids — 12 (8.8%) patients, no drug therapy — 14 (10.3%) patients. UA level significantly decreased in all groups, the average value of Δ MK and the frequency of achieving the target serum UA level were comparable. Achievement of the target serum UA level in general was in 84% of patients; in C0–1, C2, C3, C4 — in 83, 89, 82 and 81% of patients, respectively. The mean eGFR values relative to the baseline increased by the end of the study in all groups, but significant differences were only in patients with C0–1: 101.3±18.1 mL/min/1.73 m2 vs 102.8±28.6 mL/min/1.73 m2 (p=0.002). Of the 38 patients with DM2, 33 (87%) achieved the target serum UA level. In 2 patients with CKD C3, ALT and AST increased up to two norms (when taking febuxostat 120 mg/day). Conclusion: the possibility of achieving the target serum UA level when taking febuxostat (in the tablet form) in patients with gout does not depend on kidney function, including in patients with DM2. KEYWORDS: gout, febuxostat, glomerular filtration rate, chronic kidney disease, diabetes mellitus. FOR CITATION: Eliseev M.S., Zhelyabina O.V., Chikina M.N., Thakokov M.M. Febuxostat efficacy in patients with gout depending on kidney function. Russian Medical Inquiry. 2022;6(3):140–147 (in Russ.). DOI: 10.32364/2587-6821-2022-6-3-140-147.
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非布司他在痛风患者中的疗效取决于肾功能
目的:确定非布司他(片剂)治疗根据肾功能分层的痛风患者(包括2型糖尿病(DM2)患者)达到目标血清尿酸(UA)水平的概率。患者和方法:研究对象为18岁以上的痛风患者,入组前至少2周未服用非布司他或其他降尿酸药物,且血清UA水平>360 μmoL/L。所有患者均服用非布司他片剂80毫克/天。如果未达到目标血清UA水平(90 mL/min/1.73 m2),则C2 -肾功能轻度下降(60-89 mL/min/1.73 m2), C3 -肾功能中度/明显下降(30-59 mL/min/1.73 m2), C4 -肾功能明显下降(15-29 mL/min/1.73 m2)。DM2患者单独分析。随访时间至少26周:主要终点是达到目标血清UA水平,并评估eGFR趋势。结果:对136例痛风患者进行了检查。38例(27.9%)患者出现DM2。30例(22.1%)检测到CKD C0-1, 28例(20.6%)检测到C2 -, 62例(45.6%)检测到C3 -, 16例(11.8%)检测到C4 -。非布司他(片剂)在98例(72.1%)患者中以80mg /天的剂量服用,在38例(27.9%)患者中以120mg /天的剂量服用。预防性给予抗炎治疗:秋水仙碱59例(43.4%),非甾体抗炎药51例(37.5%),糖皮质激素12例(8.8%),无药物治疗14例(10.3%)。各组血清UA水平均显著降低,Δ MK平均值与达到目标血清UA水平的频率具有可比性。总体而言,84%的患者达到了目标血清UA水平;C0-1、C2、C3、C4 -分别占83%、89%、82%和81%。研究结束时,各组相对于基线的平均eGFR值均有所增加,但仅在C0-1患者中存在显著差异:101.3±18.1 mL/min/1.73 m2 vs 102.8±28.6 mL/min/1.73 m2 (p=0.002)。38例DM2患者中,33例(87%)达到目标血清UA水平。在2例CKD C3患者中,ALT和AST升高到两个标准(当服用非布司他120mg /天时)。结论:痛风患者服用非布司他(片剂)达到目标血清UA水平的可能性不依赖于肾功能,包括DM2患者。关键词:痛风、非布司他、肾小球滤过率、慢性肾病、糖尿病引用本文:Eliseev m.s., Zhelyabina o.v., chinina m.n., Thakokov M.M.。非布司他对痛风患者肾功能的影响。俄罗斯医学调查。2022;6(3):140-147(俄文)。DOI: 10.32364 / 2587-6821-2022-6-3-140-147。
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