Effects of Allopurinol on the Progression of Chronic Kidney Disease

被引:326
作者
Badve, Sunil V. [1 ,2 ,10 ]
Pascoe, Elaine M. [10 ]
Biostat, M.
Tiku, Anushree [1 ,2 ]
Boudville, Neil [10 ,13 ]
Brown, Fiona G. [14 ]
Cass, Alan [15 ]
Clarke, Philip [20 ]
Dalbeth, Nicola [21 ]
Day, Richard O. [3 ,4 ,5 ]
de Zoysa, Janak R. [21 ,22 ]
Douglas, Bettina [11 ]
Faull, Randall [16 ,17 ]
Harris, David C. [7 ,8 ]
Hawley, Carmel M. [10 ,11 ]
Jones, Graham R. D. [3 ,6 ]
Kanellis, John [14 ]
Palmer, Suetonia C. [23 ]
Perkovic, Vlado [2 ,9 ]
Rangan, Gopala K. [7 ,8 ]
Reidlinger, Donna [10 ]
Robison, Laura [10 ]
Walker, Robert J. [24 ]
Walters, Giles [18 ,19 ]
Johnson, David W. [10 ,11 ,12 ]
机构
[1] St George Hosp, Dept Renal Med, Sydney, NSW, Australia
[2] George Inst Global Hlth, Renal & Metab Div, Level 5,1 King St, Newtown, NSW 2042, Australia
[3] St Vincents Clin Sch, Sydney, NSW, Australia
[4] Univ New South Wales Med, Dept Clin Pharmacol, Sydney, NSW, Australia
[5] Univ New South Wales Med, Dept Toxicol, Sydney, NSW, Australia
[6] SydPath, Chem Pathol, Sydney, NSW, Australia
[7] Univ Sydney, St Vincents Hosp, Ctr Transplant & Renal Res, Westmead Inst Med Res, Sydney, NSW, Australia
[8] Westmead Hosp, Western Sydney Local Hlth Dist, Dept Renal Med, Sydney, NSW, Australia
[9] Royal North Shore Hosp, Dept Nephrol, Sydney, NSW, Australia
[10] Univ Queensland, Australasian Kidney Trials Network, Brisbane, Qld, Australia
[11] Princess Alexandra Hosp, Dept Nephrol, Brisbane, Qld, Australia
[12] Translat Res Inst, Brisbane, Qld, Australia
[13] Univ Western Australia, Sch Med, Perth, WA, Australia
[14] Monash Univ, Monash Med Ctr, Dept Nephrol, Melbourne, Vic, Australia
[15] Charles Darwin Univ, Menzies Sch Hlth Res, Darwin, NT, Australia
[16] Univ Adelaide, Adelaide, SA, Australia
[17] Cent Northern Adelaide Renal & Transplantat Serv, Adelaide, SA, Australia
[18] Australian Natl Univ, Sch Med, Canberra, ACT, Australia
[19] Canberra Hosp, Dept Nephrol, Canberra, ACT, Australia
[20] Univ Oxford, Nuffield Dept Populat Hlth, Hlth Econ Res Ctr, Oxford, England
[21] Univ Auckland, Dept Med, Auckland, New Zealand
[22] Waitemata Dist Hlth Board, Renal Serv, Auckland, New Zealand
[23] Univ Otago Christchurch, Dept Med, Christchurch, New Zealand
[24] Univ Otago, Dunedin Sch Med, Dunedin, New Zealand
基金
英国医学研究理事会;
关键词
ACID-LOWERING THERAPY; URIC-ACID; RENAL-DISEASE; HYPERURICEMIA; OUTCOMES; RISK;
D O I
10.1056/NEJMoa1915833
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 In this randomized, controlled trial, we randomly assigned adults with stage 3 or 4 chronic kidney disease and no history of gout who had a urinary albumin:creatinine ratio of 265 or higher (with albumin measured in milligrams and creatinine in grams) or an eGFR decrease of at least 3.0 ml per minute per 1.73 m(2) 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 Enrollment was stopped because of slow recruitment after 369 of 620 intended patients were randomly assigned to receive allopurinol (185 patients) or placebo (184 patients). Three patients per group withdrew immediately after randomization. The remaining 363 patients (mean eGFR, 31.7 ml per minute per 1.73 m(2); median urine albumin:creatinine ratio, 716.9; mean serum urate level, 8.2 mg per deciliter) were included in the assessment of the primary outcome. The change in eGFR did not differ significantly between the allopurinol group and the placebo group (-3.33 ml per minute per 1.73 m(2) per year [95% confidence interval {CI}, -4.11 to -2.55] and -3.23 ml per minute per 1.73 m(2) per year [95% CI, -3.98 to -2.47], respectively; mean difference, -0.10 ml per minute per 1.73 m(2) 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.
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收藏
页码:2504 / 2513
页数:10
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