4.4 Review

Prevention of kidney function decline using uric acid-lowering therapy in chronic kidney disease patients: a systematic review and network meta-analysis

Journal

CLINICAL RHEUMATOLOGY
Volume 41, Issue 3, Pages 911-919

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s10067-021-05956-5

Keywords

Chronic kidney disease; Febuxostat; Renoprotective effects; Topiroxostat; Uric acid-lowering therapy; Xanthine oxidase inhibitors

Categories

Funding

  1. Yokohama Foundation for Advancement of Medical Science
  2. Uehara Memorial Foundation
  3. Japan Kidney Association-Nippon Boehringer Ingelheim Joint Research Program
  4. Japan Society for the Promotion of Science
  5. Japanese Association of Dialysis Physicians
  6. Salt Science Research Foundation [20C4]
  7. Strategic Research Project of Yokohama City University

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This systematic review examined the effects of different uric acid-lowering therapy (ULT) medications on kidney function in chronic kidney disease (CKD) patients. The results suggest that Topiroxostat and febuxostat may have better renoprotective effects compared to other ULT medications in CKD patients. Further large-scale, long-term studies are needed to confirm these findings and assess their impact on dialysis induction and major adverse cardiovascular events.
Introduction Several previous studies have suggested that uric acid-lowering therapy (ULT) can slow the progression of chronic kidney disease (CKD). Although crucial for CKD patients, few studies have evaluated the effects of different ULT medications on kidney function. This systematic review summarizes evidence from randomized controlled trials (RCTs) regarding the effects of ULT on kidney function. Method We performed a systematic search of PubMed, MEDLINE, Embase, Scopus, and the Cochrane Library up to September 2021 to identify RCTs in CKD patients comparing the effects of ULT on kidney function with other ULT medications or placebo. A network meta-analysis was performed to compare each ULT indirectly. The primary outcome was a change in estimated glomerular filtration rate (eGFR) from baseline. Results Ten studies were selected with a total of 1480 patients. Topiroxostat significantly improved eGFR and reduced the urinary albumin/creatinine ratio compared to placebo (mean difference (MD) and 95% confidence interval [95% CI]: 1.49 [0.08; 2.90], P = 0.038 and 25.65% [13.25; 38.04], P < 0.001, respectively). Although febuxostat did not show a positive effect overall, it significantly improved renal function (i.e., eGFR) in a subgroup of CKD patients with hyperuricemia (MD [95% CI]: 0.85 [0.02; 1.67], P = 0.045). Allopurinol and pegloticase did not show beneficial effects. Conclusions Topiroxostat and febuxostat may have better renoprotective effects in CKD patients than other ULT medications. Further large-scale, long-term studies are required to determine whether these effects will lead, ultimately, to reductions in dialysis induction and major adverse cardiovascular events.

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