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Renoprotective effects of febuxostat compared with allopurinol in patients with hyperuricemia: A systematic review and meta-analysis

Authors
Kim, SollipKim, Hyun-JungAhn, Hyeong-SikOh, Se WonHan, Kum HyunUm, Tae-HyunCho, Chong-RaeHan, Sang Youb
Issue Date
9월-2017
Publisher
KOREAN SOC NEPHROLOGY
Keywords
Chronic kidney disease; Febuxostat; Gout; Hyperuricemia; Meta-analysis
Citation
KIDNEY RESEARCH AND CLINICAL PRACTICE, v.36, no.3, pp.274 - 281
Indexed
SCOPUS
KCI
Journal Title
KIDNEY RESEARCH AND CLINICAL PRACTICE
Volume
36
Number
3
Start Page
274
End Page
281
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/82378
DOI
10.23876/j.krcp.2017.36.3.274
ISSN
2211-9132
Abstract
Background: 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. Methods: 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. Results: 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(2), 95% confidence interval [CI] 0.38, 2.91 mL/min/1.73 m(2); heterogeneity chi(2) = 1.25, I-2 = 0%, P = 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 chi(2) = 0.81, I-2 = 0%, P = 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 chi(2) = 6.24, I-2 = 52%, P < 0.001). Conclusion: Febuxostat might be more renoprotective than allopurinol.
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