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Canagliflozin and Kidney-Related Adverse Events in Type 2 Diabetes and CKD: Findings From the Randomized CREDENCE Trial

Authors :
Heerspink, HJL
Oshima, M
Zhang, H
Li, J
Agarwal, R
Capuano, G
Charytan, DM
Craig, J
de Zeeuw, D
Di Tanna, GL ; https://orcid.org/0000-0002-5470-3567
Levin, A
Neal, B ; https://orcid.org/0000-0002-0490-7465
Perkovic, V ; https://orcid.org/0000-0002-4257-7620
Wheeler, DC
Yavin, Y
Jardine, MJ ; https://orcid.org/0000-0002-0160-2375
Heerspink, HJL
Oshima, M
Zhang, H
Li, J
Agarwal, R
Capuano, G
Charytan, DM
Craig, J
de Zeeuw, D
Di Tanna, GL ; https://orcid.org/0000-0002-5470-3567
Levin, A
Neal, B ; https://orcid.org/0000-0002-0490-7465
Perkovic, V ; https://orcid.org/0000-0002-4257-7620
Wheeler, DC
Yavin, Y
Jardine, MJ ; https://orcid.org/0000-0002-0160-2375
Source :
urn:ISSN:0272-6386; urn:ISSN:1523-6838; American Journal of Kidney Diseases, 79, 2, 244-256.e1
Publication Year :
2022

Abstract

Rationale & Objective: Canagliflozin reduced the risk of kidney failure and related outcomes in patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD) in the CREDENCE (Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation) trial. This analysis of CREDENCE trial data examines the effect of canagliflozin on the incidence of kidney-related adverse events (AEs). Study Design: A randomized, double-blind, placebo-controlled, multicenter international trial. Setting & Participants: 4,401 trial participants with T2DM, CKD, and urinary albumin-creatinine ratio >300-5,000 mg/g. Interventions: Participants were randomly assigned to receive canagliflozin 100 mg/d or placebo. Outcomes: Rates of kidney-related AEs were analyzed using an on-treatment approach, overall and by screening estimated glomerular filtration rate (eGFR) strata (30-<45, 45-<60, and 60-<90 mL/min/1.73 m2). Results: Canagliflozin was associated with a reduction in the overall incidence rate of kidney-related AEs (60.2 vs 84.0 per 1,000 patient-years; hazard ratio [HR], 0.71 [95% CI, 0.61-0.82]; P < 0.001), with consistent results for serious kidney-related AEs (HR, 0.72 [95% CI, 0.51-1.00]; P = 0.05) and acute kidney injury (AKI; HR, 0.85 [95% CI, 0.64-1.13]; P = 0.3). The rates of kidney-related AEs were lower with canagliflozin relative to placebo across the 3 eGFR strata (HRs of 0.73, 0.60, and 0.81 for eGFR 30-<45, 45-<60, and 60-<90 mL/min/1.73 m2, respectively; P = 0.3 for interaction), with similar results for AKI (P = 0.9 for interaction). Full recovery of kidney function within 30 days after an AKI event occurred more frequently with canagliflozin versus placebo (53.1% vs 35.4%; odds ratio, 2.2 [95% CI, 1.0-4.7]; P = 0.04). Limitations: Kidney-related AEs including AKI were investigator-reported and collected without central adjudication. Biomarkers of AKI and structural tubular damage were not measured, and creatinine data after an AKI ev

Details

Database :
OAIster
Journal :
urn:ISSN:0272-6386; urn:ISSN:1523-6838; American Journal of Kidney Diseases, 79, 2, 244-256.e1
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1259604245
Document Type :
Electronic Resource