Serum Urate Lowering with Allopurinol and Kidney Function in Type 1 Diabetes

Alessandro Doria(Joslin Diabetes Center), Andrzej T. Gałecki(Joslin Diabetes Center), Cathie Spino(Joslin Diabetes Center), Rodica Pop‐Busui(Joslin Diabetes Center), David Z.I. Cherney(Joslin Diabetes Center), Ildiko Lingvay(Joslin Diabetes Center), Afshin Parsa(Joslin Diabetes Center), Peter Rossing(Joslin Diabetes Center), Ronald J. Sigal(Joslin Diabetes Center), Maryam Afkarian(Joslin Diabetes Center), Ronnie Aronson(Joslin Diabetes Center), Maria Luiza Caramori(Joslin Diabetes Center), Jill P. Crandall(Joslin Diabetes Center), Ian H. de Boer(Joslin Diabetes Center), Thomas G. Elliott(Joslin Diabetes Center), Allison B. Goldfine(Joslin Diabetes Center), J. Sonya Haw(Joslin Diabetes Center), Irl B. Hirsch(Joslin Diabetes Center), Amy B. Karger(Joslin Diabetes Center), David M. Maahs(Joslin Diabetes Center), Janet B. McGill(Joslin Diabetes Center), Mark E. Molitch(Northwestern University), Bruce A. Perkins(Joslin Diabetes Center), Sarit Polsky(Joslin Diabetes Center), Marlon Pragnell(Joslin Diabetes Center), William N. Robiner(Joslin Diabetes Center), Sylvia E. Rosas(Joslin Diabetes Center), Peter Senior(Joslin Diabetes Center), Katherine R. Tuttle(Joslin Diabetes Center), Guillermo E. Umpierrez(Joslin Diabetes Center), Amisha Wallia(Northwestern University), Ruth S. Weinstock(Joslin Diabetes Center), Chun-Yi Wu(Joslin Diabetes Center), Michael Mauer(Joslin Diabetes Center)
New England Journal of Medicine
June 24, 2020
Cited by 355Open Access
Full Text

Abstract

BACKGROUND: Higher serum urate levels are associated with an increased risk of diabetic kidney disease. Lowering of the serum urate level with allopurinol may slow the decrease in the glomerular filtration rate (GFR) in persons with type 1 diabetes and early-to-moderate diabetic kidney disease. METHODS: of body-surface area, and evidence of diabetic kidney disease to receive allopurinol or placebo. The primary outcome was the baseline-adjusted GFR, as measured with iohexol, after 3 years plus a 2-month washout period. Secondary outcomes included the decrease in the iohexol-based GFR per year and the urinary albumin excretion rate after washout. Safety was also assessed. RESULTS: per year; 95% CI, -1.5 to 0.4). The mean urinary albumin excretion rate after washout was 40% (95% CI, 0 to 80) higher with allopurinol than with placebo. The frequency of serious adverse events was similar in the two groups. CONCLUSIONS: We found no evidence of clinically meaningful benefits of serum urate reduction with allopurinol on kidney outcomes among patients with type 1 diabetes and early-to-moderate diabetic kidney disease. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases and others; PERL ClinicalTrials.gov number, NCT02017171.).


Related Papers

No related papers found

Powered by citation graph analysis