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Cited 27 time in webofscience Cited 33 time in scopus
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Comparison of renoprotective effects of febuxostat and allopurinol in hyperuricemic patients with chronic kidney disease

Authors
Lee, Jang-WookLee, Kwang-Hoon
Issue Date
Mar-2019
Publisher
SPRINGER
Keywords
Febuxostat; Allopurinol; Hyperuricemia; Renal insufficiency
Citation
INTERNATIONAL UROLOGY AND NEPHROLOGY, v.51, no.3, pp 467 - 473
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL UROLOGY AND NEPHROLOGY
Volume
51
Number
3
Start Page
467
End Page
473
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/8378
DOI
10.1007/s11255-018-2051-2
ISSN
0301-1623
1573-2584
Abstract
PurposeThis 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.Methods141 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.ResultsOverall, mean age was 62.613.3 years, baseline eGFR 42.1 +/- 8.8mL/min/1.73m(2), and serum uric acid 8.6 +/- 1.5mg/dL without intergroup difference. During the observation period (55.9 +/- 31.8months), 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 +/- 0.8mg/dL, p<0.001) and maintained significantly higher mean eGFR values consistently for 4years. 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.
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