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Uric acid lowering for slowing CKD progression after the CKD-FIX trial: a solved question or still a dilemma?
Author(s) -
Giovanna Leoncini,
Cecilia Barnini,
Luca Manco,
Alessandro Nobili,
Daniele Dotta,
Martina Penso,
Elisa Russo,
Francesca Cappadona,
Francesca Viazzi,
Roberto Pontremoli
Publication year - 2022
Publication title -
clinical kidney journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.033
H-Index - 40
eISSN - 2048-8513
pISSN - 2048-8505
DOI - 10.1093/ckj/sfac075
Subject(s) - febuxostat , medicine , hyperuricemia , uric acid , gout , allopurinol , xanthine oxidase inhibitor , kidney disease , intensive care medicine , randomized controlled trial , xanthine oxidase , disease , clinical trial , bioinformatics , biochemistry , chemistry , biology , enzyme
Hyperuricemia has been associated with several cardiovascular risk factors and is a well-known predictor of kidney disease. In vitro studies as well as animal models highlighted a role for uric acid in the development and progression of haemodynamic and tissue damage at the renal level leading to glomerular and tubulointerstitial abnormalities. Urate-lowering treatment, especially by xanthine oxidase inhibitors, has been proposed in order to improve kidney outcomes. However, recent randomized controlled trials failed to demonstrate a beneficial effect of allopurinol or febuxostat on renal disease, casting doubts on the role of this therapeutical approach to improve nephroprotection. We provide a critical overview of current literature on this topic and offer a possible interpretation of results from recent intervention trials with urate-lowering treatment on renal outcomes.

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