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Urate-lowering efficacy and renal safety of febuxostat in patients with hyperuricemia and stage 4–5 chronic kidney disease not yet on dialysis: A meta-analysis of observational studies

The efficacy and safety of febuxostat in patients with stage 4–5 chronic kidney disease (CKD) remains unclear. We evaluated the urate-lowering efficacy and renal safety of febuxostat in patients with stage 4–5 CKD not yet on dialysis, through a meta-analysis of observational studies. We performed a...

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Published in:Seminars in arthritis and rheumatism 2022-10, Vol.56, p.152073-152073, Article 152073
Main Authors: Jeong, Hye-Jin, Park, Woo Yeong, Kim, Sang-Hyon, Dalbeth, Nicola, Son, Chang-Nam
Format: Article
Language:English
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Summary:The efficacy and safety of febuxostat in patients with stage 4–5 chronic kidney disease (CKD) remains unclear. We evaluated the urate-lowering efficacy and renal safety of febuxostat in patients with stage 4–5 CKD not yet on dialysis, through a meta-analysis of observational studies. We performed a systematic search in PubMed, Ovid MEDLINE, Embase, and the Cochrane Library databases for observational studies of patients with advanced CKD starting febuxostat. Articles describing changes in serum urate levels and/or renal function assessed by the estimated glomerular filtration rate (eGFR) were included. Among 148 retrieved studies, five relevant observational studies with 327 patients were included in the meta-analysis. Febuxostat was administered daily at 10–120 mg for 3–12 months. Serum urate reduced in response to febuxostat (weighted mean difference, -1.85 mg/dL; 95% CI, -2.04–-1.67 mg/dL; I2; 0%). Three studies involving 145 patients included eGFR assessments. Renal function, assessed through the eGFR, did not change after febuxostat use (weighted mean difference, 0.11 mL/min/1.73m2; 95% CI, -0.25–0.47 mL/min/1.73m2; I2; 45%). Overall, febuxostat has acceptable urate-lowering efficacy and renal safety in patients with hyperuricemia and stage 4–5 CKD who are not yet on dialysis.
ISSN:0049-0172
1532-866X
DOI:10.1016/j.semarthrit.2022.152073