Kim Sollip, Kim Hyun-Jung, Ahn Hyeong-Sik, Oh Se Won, Han Kum Hyun, Um Tae-Hyun, Cho Chong-Rae, Han Sang Youb
Department of Laboratory Medicine, Ilsan Paik Hospital, Inje University College of Medicine, Goyang, Korea.
Department of Preventive Medicine, Korea University College of Medicine, Seoul, Korea.
Kidney Res Clin Pract. 2017 Sep;36(3):274-281. doi: 10.23876/j.krcp.2017.36.3.274. Epub 2017 Sep 30.
Hyperuricemia is reported to be related to rapid progression of renal function in patients with chronic kidney disease (CKD). Allopurinol, a uric acid lowering agent, protects renal progression. However, it is not widely used in patients with CKD because of its serious adverse event. Febuxostat can be alternatively used for patients who are intolerable to allopurinol. We aimed to determine renoprotective effect and urate-lowering effect between the two drugs.
We performed a systematic review and meta-analysis of randomized controlled trials to assess the effects of febuxostat compared to allopurinol in patients with hyperuricemia. MEDLINE, Embase, and Cochrane Library databases were searched to identify research publications.
Four relevant publications were selected from among 3,815 studies. No significant differences were found in the changes in serum creatinine from baseline between the febuxostat and allopurinol groups. Changes in estimated glomerular filtration rate (eGFR) were observed between the two groups at 1 month (mean difference 1.65 mL/min/1.73 m, 95% confidence interval [CI] 0.38, 2.91 mL/min/1.73 m; heterogeneity χ = 1.25, I = 0%, = 0.01); however, the changes in eGFR were not significantly different at 3 months. A significant difference did exist in the changes in albuminuria levels from baseline between the febuxostat and allopurinol groups (mean difference -80.47 mg/gCr, 95% CI -149.29, -11.64 mg/gCr; heterogeneity χ = 0.81, I = 0%, = 0.02). A significant difference was also observed in the changes in serum uric acid from baseline between the febuxostat and allopurinol groups (mean difference -0.92 mg/dL, 95% CI -1.29, -0.56 mg/dL; heterogeneity χ = 6.24, I = 52%, < 0.001).
Febuxostat might be more renoprotective than allopurinol.
据报道,高尿酸血症与慢性肾脏病(CKD)患者肾功能的快速进展有关。尿酸降低剂别嘌醇可保护肾脏进展。然而,由于其严重的不良事件,它在CKD患者中并未广泛使用。对于不能耐受别嘌醇的患者,非布司他可作为替代药物使用。我们旨在确定这两种药物的肾脏保护作用和降尿酸作用。
我们对随机对照试验进行了系统评价和荟萃分析,以评估非布司他与别嘌醇相比对高尿酸血症患者的影响。检索了MEDLINE、Embase和Cochrane图书馆数据库以识别研究出版物。
从3815项研究中筛选出4篇相关出版物。非布司他组和别嘌醇组血清肌酐相对于基线的变化无显著差异。两组在1个月时观察到估计肾小球滤过率(eGFR)的变化(平均差异1.65 mL/min/1.73 m²,95%置信区间[CI] 0.38,2.91 mL/min/1.73 m²;异质性χ² = 1.25,I² = 0%,P = 0.01);然而,3个月时eGFR的变化无显著差异。非布司他组和别嘌醇组蛋白尿水平相对于基线的变化存在显著差异(平均差异 -80.47 mg/gCr,95% CI -149.29,-11.64 mg/gCr;异质性χ² = 0.81,I² = 0%,P = 0.02)。非布司他组和别嘌醇组血清尿酸相对于基线的变化也观察到显著差异(平均差异 -0.92 mg/dL,95% CI -1.29,-0.56 mg/dL;异质性χ² = 6.24,I² = 52%,P < 0.001)。
非布司他可能比别嘌醇具有更强的肾脏保护作用。