Your browser doesn't support javascript.
loading
Cardiovascular Effects of Canagliflozin in Relation to Renal Function and Albuminuria.
Sarraju, Ashish; Bakris, George; Cannon, Christopher P; Cherney, David; Damaraju, C V; Figtree, Gemma A; Gogate, Jagadish; Greene, Tom; Heerspink, Hiddo J L; Januzzi, James L; Neal, Bruce; Jardine, Meg J; Blais, Jaime; Kosiborod, Mikhail; Levin, Adeera; Lingvay, Ildiko; Weir, Matthew R; Perkovic, Vlado; Mahaffey, Kenneth W.
Afiliação
  • Sarraju A; Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Bakris G; Department of Medicine, University of Chicago Medicine, Chicago, Illinois, USA.
  • Cannon CP; Cardiovascular Division, Brigham & Women's Hospital and Baim Institute for Clinical Research, Boston, Massachusetts, USA.
  • Cherney D; University of Toronto, Toronto, Ontario, Canada.
  • Damaraju CV; Janssen Scientific Affairs, LLC, Titusville, New Jersey, USA.
  • Figtree GA; Kolling Institute, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Gogate J; Janssen Scientific Affairs, LLC, Titusville, New Jersey, USA.
  • Greene T; Division of Biostatistics, Department of Population Health Sciences, University of Utah, Salt Lake City, Utah, USA.
  • Heerspink HJL; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Januzzi JL; Massachusetts General Hospital and Baim Institute for Clinical Research, Boston, Massachusetts, USA.
  • Neal B; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.
  • Jardine MJ; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; Concord Repatriation General Hospital, Sydney, New South Wales, Australia; NHMRC Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia.
  • Blais J; Janssen Scientific Affairs, LLC, Titusville, New Jersey, USA.
  • Kosiborod M; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, Missouri, USA.
  • Levin A; Division of Nephrology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lingvay I; University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Weir MR; Division of Nephrology, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Perkovic V; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia; The Royal North Shore Hospital, Sydney, New South Wales, Australia.
  • Mahaffey KW; Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA. Electronic address: kenneth.mahaffey@stanford.edu.
J Am Coll Cardiol ; 80(18): 1721-1731, 2022 11 01.
Article em En | MEDLINE | ID: mdl-36302584
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 albumincreatinine 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 [CANVAS-R], NCT01989754; and Evaluation of the Effects of Canagliflozin on Renal and Cardiovascular Outcomes in Participants With Diabetic Nephropathy [CREDENCE], NCT02065791).
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Nefropatias Diabéticas / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos