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Effects of Allopurinol on the Progression of Chronic Kidney Disease

Sunil V. Badve, Elaine M. Pascoe, Anushree Tiku, Neil C Boudville, Fiona G. Brown, Alan Cass, Philip Clarke, Nicola Dalbeth, Richard Osborne Day, Janak de Zoysa, Bettina Douglas, Randall Faull, David C.H. Harris, Carmel Mary Hawley, Graham R.D. Jones, John Kanellis, Suetonia C. Palmer, Vlado Perkovic, Gopala K. Rangan, Donna M. Reidlinger, Laura E. Robison, Robert James Walker, Giles Desmond Walters, David Wayne Johnson

📄 Abstract

BACKGROUND: Elevated serum urate levels are associated with progression of chronic kidney disease. Whether urate-lowering treatment with allopurinol can attenuate the decline of the estimated glomerular filtration rate (eGFR) in patients with chronic kidney disease who are at risk for progression is not known. METHODS: of body-surface area in the preceding year to receive allopurinol (100 to 300 mg daily) or placebo. The primary outcome was the change in eGFR from randomization to week 104, calculated with the Chronic Kidney Disease Epidemiology Collaboration creatinine equation. RESULTS: per year [95% CI, -1.18 to 0.97]; P = 0.85). Serious adverse events were reported in 84 of 182 patients (46%) in the allopurinol group and in 79 of 181 patients (44%) in the placebo group. CONCLUSIONS: In patients with chronic kidney disease and a high risk of progression, urate-lowering treatment with allopurinol did not slow the decline in eGFR as compared with placebo. (Funded by the National Health and Medical Research Council of Australia and the Health Research Council of New Zealand; CKD-FIX Australian New Zealand Clinical Trials Registry number, ACTRN12611000791932.).

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