Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy

Vlado Perkovic(North Shore Hospital), Meg Jardine(Concord Repatriation General Hospital), Bruce Neal(The University of Sydney), Séverine Bompoint(UNSW Sydney), Hiddo J.L. Heerspink(University of Groningen), David M. Charytan(Baim Institute for Clinical Research), Robert Edwards(Janssen (United States)), Rajiv Agarwal(Indiana University School of Medicine), George L. Bakris(University of Chicago), Scott Bull(Janssen (United States)), Christopher P. Cannon(Baim Institute for Clinical Research), George Capuano(Janssen (United States)), Pei-Ling Chu(Janssen (United States)), Dick de Zeeuw(University of Groningen), Tom Greene(University of Utah), Adeera Levin(University of British Columbia), Carol A. Pollock(Royal North Shore Hospital), David C. Wheeler, Yshai Yavin(Janssen (United States)), Hong Zhang(Peking University), Bernard Zinman(University of Toronto), Gary Meininger(Janssen (United States)), Barry M. Brenner(Baim Institute for Clinical Research), Kenneth W. Mahaffey(Stanford University)
New England Journal of Medicine
April 14, 2019
Cited by 5,940Open Access
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Abstract

BACKGROUND: Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium-glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes. METHODS: ), a doubling of the serum creatinine level, or death from renal or cardiovascular causes. Prespecified secondary outcomes were tested hierarchically. RESULTS: The trial was stopped early after a planned interim analysis on the recommendation of the data and safety monitoring committee. At that time, 4401 patients had undergone randomization, with a median follow-up of 2.62 years. The relative risk of the primary outcome was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively (hazard ratio, 0.70; 95% confidence interval [CI], 0.59 to 0.82; P = 0.00001). The relative risk of the renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; P = 0.002). The canagliflozin group also had a lower risk of cardiovascular death, myocardial infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P = 0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001). There were no significant differences in rates of amputation or fracture. CONCLUSIONS: In patients with type 2 diabetes and kidney disease, the risk of kidney failure and cardiovascular events was lower in the canagliflozin group than in the placebo group at a median follow-up of 2.62 years. (Funded by Janssen Research and Development; CREDENCE ClinicalTrials.gov number, NCT02065791.).


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