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降尿酸治疗对慢性肾脏病患者的疗效:一项随机对照试验的网络荟萃分析。

Efficacy of Urate-Lowering Therapy in Patients With Chronic Kidney Disease: A Network Meta-Analysis of Randomized Controlled Trials.

机构信息

Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu, China.

Changshu Hospital affiliated to Nanjing University of Chinese Medicine, Jiangsu, China.

出版信息

Clin Ther. 2022 May;44(5):723-735.e6. doi: 10.1016/j.clinthera.2022.03.014. Epub 2022 May 22.

DOI:10.1016/j.clinthera.2022.03.014
PMID:35610080
Abstract

PURPOSE

The goal of this study was to systematically review the efficacy and safety of urate-lowering therapy in patients with chronic kidney disease (CKD).

METHODS

PubMed, the Cochrane Central Registration of Controlled Trials, and EMBASE databases and several websites were electronically searched to collect randomized clinical trials on the efficacy of urate-lowering therapy in CKD from inception to December 31, 2020. The key primary end points were uric acid or estimated glomerular filtration rate (eGFR) levels; the safety end points were death, renal event, cardiovascular event, and gastrointestinal event. A Bayesian network meta-analysis was conducted with the use of ADDIS and R software.

FINDINGS

A total of 17 randomized clinical trials involving 2059 patients were included. The results of network meta-analysis showed that urate-lowering therapy could reduce urate levels in patients with CKD. Febuxostat was the most effective treatment in lowering urate levels according to the rank probability. Urate-lowering therapy has the tendency to delay the decline of eGFR, but the difference was not statistically significant. Ranking probability showed that benzbromarone, febuxostat, and allopurinol ranked higher than placebo in reducing the decline of eGFR. There were no statistically significant differences between groups in the incidence of all adverse effects.

IMPLICATIONS

All urate-lowering therapies could reduce the urate level in patients with CKD, but the benefit of such therapy in renal disease is still unclear. PROSPERO identifier: CRD42020222601.

摘要

目的

本研究旨在系统评价降尿酸治疗在慢性肾脏病(CKD)患者中的疗效和安全性。

方法

通过电子检索 PubMed、Cochrane 中心对照试验注册库、EMBASE 数据库以及其他几个网站,收集截至 2020 年 12 月 31 日降尿酸治疗 CKD 的疗效的随机临床试验。主要疗效终点为尿酸或估算肾小球滤过率(eGFR)水平;安全性终点为死亡、肾脏事件、心血管事件和胃肠道事件。采用 ADDIS 和 R 软件进行贝叶斯网状荟萃分析。

发现

共纳入 17 项随机临床试验,涉及 2059 例患者。网状荟萃分析结果显示,降尿酸治疗可降低 CKD 患者的尿酸水平。非布司他是降尿酸水平最有效的治疗方法,根据秩概率排名第一。降尿酸治疗有延缓 eGFR 下降的趋势,但差异无统计学意义。秩概率表明,苯溴马隆、非布司他和别嘌醇在降低 eGFR 下降方面的排名高于安慰剂。各组之间所有不良反应的发生率无统计学差异。

结论

所有降尿酸治疗均可降低 CKD 患者的尿酸水平,但此类治疗对肾脏疾病的益处尚不清楚。PROSPERO 标识符:CRD42020222601。

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