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比较别嘌醇和非布司他在高尿酸血症慢性肾脏病患者中的护肾作用。

Comparison of renoprotective effects of febuxostat and allopurinol in hyperuricemic patients with chronic kidney disease.

机构信息

Department of Internal Medicine, Dongguk University Ilsan Hospital, Goyang, South Korea.

出版信息

Int Urol Nephrol. 2019 Mar;51(3):467-473. doi: 10.1007/s11255-018-2051-2. Epub 2019 Jan 2.

Abstract

PURPOSE

This study aimed to compare the renoprotective effect between febuxostat and allopurinol in hyperuricemic patients with chronic kidney disease (CKD), about which limited data are available.

METHODS

141 patients with stage 3 CKD and hyperuricemia were followed from June 2005 to April 2018. Thirty patients received febuxostat, 40 allopurinol and 71 conventional CKD management only (control group). We compared the mean serum uric acid levels, estimated glomerular filtration rate (eGFR) changes over time and renal survival time free from predefined renal disease progression among these 3 groups.

RESULTS

Overall, mean age was 62.6 ± 13.3 years, baseline eGFR 42.1 ± 8.8 mL/min/1.73 m, and serum uric acid 8.6 ± 1.5 mg/dL without intergroup difference. During the observation period (55.9 ± 31.8 months), febuxostat group, compared to both allopurinol and control group, had significantly lower mean serum uric acid levels (5.7 ± 1.0 vs. 7.1 ± 1.2 vs. 8.0 ± 0.8 mg/dL, p < 0.001) and maintained significantly higher mean eGFR values consistently for 4 years. Febuxostat group had significantly longer renal survival time free from renal disease progression than allopurinol and control group (87.7 (95% CI 71.2-104.2) vs. 77.6 (95% CI 60.2-94.9) vs. 48.7 (95% CI 39.3-58.1) months, respectively, p < 0.001). Cox proportional hazard model analysis adjusting for potent confounders revealed that febuxostat, with control group as reference, significantly reduced the risk of renal disease progression by 74.3% (hazard ratio 0.257 (95% CI 0.072-0.912), p = 0.036), while allopurinol showed insignificant result.

CONCLUSIONS

Febuxostat seems to reduce serum uric acid level and to retard renal disease progression more effectively than allopurinol in hyperuricemic patients with CKD.

摘要

目的

本研究旨在比较别嘌醇和非布司他在伴有慢性肾脏病(CKD)的高尿酸血症患者中的肾脏保护作用,目前这方面的数据有限。

方法

纳入 2005 年 6 月至 2018 年 4 月期间 141 例 CKD 3 期合并高尿酸血症的患者,其中 30 例接受非布司他治疗,40 例接受别嘌醇治疗,71 例仅接受常规 CKD 管理(对照组)。比较三组患者的平均血尿酸水平、估算肾小球滤过率(eGFR)随时间的变化以及无预定义肾脏疾病进展的肾脏生存时间。

结果

总体而言,患者平均年龄为 62.6±13.3 岁,基线 eGFR 为 42.1±8.8 mL/min/1.73 m,血尿酸为 8.6±1.5 mg/dL,三组间无差异。在观察期间(55.9±31.8 个月),与别嘌醇组和对照组相比,非布司他组的平均血尿酸水平显著降低(5.7±1.0 vs. 7.1±1.2 vs. 8.0±0.8 mg/dL,p<0.001),且 eGFR 均值在 4 年内持续升高。与别嘌醇组和对照组相比,非布司他组的肾脏无疾病进展生存时间显著延长(87.7(95%CI 71.2-104.2)vs. 77.6(95%CI 60.2-94.9)vs. 48.7(95%CI 39.3-58.1)个月,p<0.001)。经多因素校正的 Cox 比例风险模型分析显示,以对照组为参考,非布司他可使肾脏疾病进展的风险降低 74.3%(风险比 0.257(95%CI 0.072-0.912),p=0.036),而别嘌醇则无显著结果。

结论

在伴有 CKD 的高尿酸血症患者中,非布司他似乎比别嘌醇更能有效降低血尿酸水平,延缓肾脏疾病的进展。

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