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Cardiovascular Effects of Canagliflozin in Relation to Renal Function and Albuminuria

Authors :
Sarraju, A
Bakris, G
Cannon, CP
Cherney, D
Damaraju, CV
Figtree, GA
Gogate, J
Greene, T
Heerspink, HJL
Januzzi, JL
Neal, B ; https://orcid.org/0000-0002-0490-7465
Jardine, MJ ; https://orcid.org/0000-0002-0160-2375
Blais, J
Kosiborod, M
Levin, A
Lingvay, I
Weir, MR
Perkovic, V ; https://orcid.org/0000-0002-4257-7620
Mahaffey, KW
Sarraju, A
Bakris, G
Cannon, CP
Cherney, D
Damaraju, CV
Figtree, GA
Gogate, J
Greene, T
Heerspink, HJL
Januzzi, JL
Neal, B ; https://orcid.org/0000-0002-0490-7465
Jardine, MJ ; https://orcid.org/0000-0002-0160-2375
Blais, J
Kosiborod, M
Levin, A
Lingvay, I
Weir, MR
Perkovic, V ; https://orcid.org/0000-0002-4257-7620
Mahaffey, KW
Source :
urn:ISSN:0735-1097; urn:ISSN:1558-3597; Journal of the American College of Cardiology, 80, 18, 1721-1731
Publication Year :
2022

Abstract

Background: People with type 2 diabetes mellitus (T2DM) have elevated cardiovascular (CV) risk, including for hospitalization for heart failure (HHF). Canagliflozin reduced CV and kidney events in patients with T2DM and high CV risk or nephropathy in the CANVAS (CANagliflozin cardioVascular Assessment Study) Program and the CREDENCE (Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation) trial. Objectives: The aim of this study was to assess the effects of canagliflozin on CV outcomes according to baseline estimated glomerular filtration rate (eGFR) and urine albumin:creatinine ratio (UACR) in pooled patient-level data from the CANVAS Program and CREDENCE trial. Methods: Canagliflozin effects on CV death or HHF were assessed by baseline eGFR (<45, 45-60, and >60 mL/min/1.73 m2) and UACR (<30, 30-300, and >300 mg/g). HRs and 95% CIs were estimated by using Cox regression models overall and according to subgroups. Results: A total of 14,543 participants from the CANVAS Program (N = 10,142) and the CREDENCE (N = 4,401) trial were included, with a mean age of 63 years, 35% female, 75% White, 13.2% with baseline eGFR <45 mL/min/1.73 m2, and 31.9% with UACR >300 mg/g. Rates of CV death or HHF increased as eGFR declined and/or UACR increased. Canagliflozin significantly reduced CV death or HHF compared with placebo (19.4 vs 28.0 events per 1,000 patient-years; HR: 0.70; 95% CI: 0.62-0.79), with consistent results across eGFR and UACR categories (all P interaction >0.40). Conclusions: Risk of CV death or HHF was higher in those with lower baseline eGFR and/or higher UACR. Canagliflozin consistently reduced CV death or HHF in participants with T2DM and high CV risk or nephropathy regardless of baseline renal function or level of albuminuria. (Canagliflozin Cardiovascular Assessment Study [CANVAS], NCT01032629; A Study of the Effects of Canagliflozin [JNJ-24831754] on Renal Endpoints in Adult Participants With Type 2 Diabetes Mellitus [CA

Details

Database :
OAIster
Journal :
urn:ISSN:0735-1097; urn:ISSN:1558-3597; Journal of the American College of Cardiology, 80, 18, 1721-1731
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1458863353
Document Type :
Electronic Resource