Effects of Allopurinol on the Progression of Chronic Kidney Disease

Sunil V. Badve(The University of Queensland), Elaine M. Pascoe(The University of Queensland), Anushree Tiku(St Vincent Hospital), Neil Boudville(The University of Queensland), Fiona G. Brown(St Vincent Hospital), Alan Cass(St Vincent Hospital), Philip Clarke(St Vincent Hospital), Nicola Dalbeth(University of Auckland), Richard O. Day(St Vincent Hospital), Janak de Zoysa(University of Auckland), Bettina Douglas(St Vincent Hospital), Randall Faull(St Vincent Hospital), David C.H. Harris(St Vincent Hospital), Carmel M. Hawley(The University of Queensland), Graham Jones(St Vincent Hospital), John Kanellis(St Vincent Hospital), Suetonia C. Palmer(St Vincent Hospital), Vlado Perkovic(St Vincent Hospital), Gopala K. Rangan(St Vincent Hospital), Donna Reidlinger(The University of Queensland), Laura Robison(The University of Queensland), Robert Walker(St Vincent Hospital), Giles Walters(Australian National University), David W. Johnson(Translational Research Institute)
New England Journal of Medicine
June 24, 2020
Cited by 448Open Access
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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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