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Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program
BACKGROUND: Canagliflozin is a sodium glucose cotransporter 2 inhibitor that reduces the risk of cardiovascular events. We report the effects on heart failure (HF) and cardiovascular death overall, in those with and without a baseline history of HF, and in other participant subgroups. METHODS: The C...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075881/ https://www.ncbi.nlm.nih.gov/pubmed/29526832 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.034222 |
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author | Rådholm, Karin Figtree, Gemma Perkovic, Vlado Solomon, Scott D. Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Barrett, Terrance D. Shaw, Wayne Desai, Mehul Matthews, David R. Neal, Bruce |
author_facet | Rådholm, Karin Figtree, Gemma Perkovic, Vlado Solomon, Scott D. Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Barrett, Terrance D. Shaw, Wayne Desai, Mehul Matthews, David R. Neal, Bruce |
author_sort | Rådholm, Karin |
collection | PubMed |
description | BACKGROUND: Canagliflozin is a sodium glucose cotransporter 2 inhibitor that reduces the risk of cardiovascular events. We report the effects on heart failure (HF) and cardiovascular death overall, in those with and without a baseline history of HF, and in other participant subgroups. METHODS: The CANVAS Program (Canagliflozin Cardiovascular Assessment Study) enrolled 10 142 participants with type 2 diabetes mellitus and high cardiovascular risk. Participants were randomly assigned to canagliflozin or placebo and followed for a mean of 188 weeks. The primary end point for these analyses was adjudicated cardiovascular death or hospitalized HF. RESULTS: Participants with a history of HF at baseline (14.4%) were more frequently women, white, and hypertensive and had a history of prior cardiovascular disease (all P<0.001). Greater proportions of these patients were using therapies such as blockers of the renin angiotensin aldosterone system, diuretics, and β-blockers at baseline (all P<0.001). Overall, cardiovascular death or hospitalized HF was reduced in those treated with canagliflozin compared with placebo (16.3 versus 20.8 per 1000 patient-years; hazard ratio [HR], 0.78; 95% confidence interval [CI], 0.67–0.91), as was fatal or hospitalized HF (HR, 0.70; 95% CI, 0.55–0.89) and hospitalized HF alone (HR, 0.67; 95% CI, 0.52–0.87). The benefit on cardiovascular death or hospitalized HF may be greater in patients with a prior history of HF (HR, 0.61; 95% CI, 0.46–0.80) compared with those without HF at baseline (HR, 0.87; 95% CI, 0.72–1.06; P interaction =0.021). The effects of canagliflozin compared with placebo on other cardiovascular outcomes and key safety outcomes were similar in participants with and without HF at baseline (all interaction P values >0.130), except for a possibly reduced absolute rate of events attributable to osmotic diuresis among those with a prior history of HF (P=0.03). CONCLUSIONS: In patients with type 2 diabetes mellitus and an elevated risk of cardiovascular disease, canagliflozin reduced the risk of cardiovascular death or hospitalized HF across a broad range of different patient subgroups. Benefits may be greater in those with a history of HF at baseline. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01032629 and NCT01989754. |
format | Online Article Text |
id | pubmed-6075881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-60758812018-08-17 Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program Rådholm, Karin Figtree, Gemma Perkovic, Vlado Solomon, Scott D. Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Barrett, Terrance D. Shaw, Wayne Desai, Mehul Matthews, David R. Neal, Bruce Circulation Original Research Articles BACKGROUND: Canagliflozin is a sodium glucose cotransporter 2 inhibitor that reduces the risk of cardiovascular events. We report the effects on heart failure (HF) and cardiovascular death overall, in those with and without a baseline history of HF, and in other participant subgroups. METHODS: The CANVAS Program (Canagliflozin Cardiovascular Assessment Study) enrolled 10 142 participants with type 2 diabetes mellitus and high cardiovascular risk. Participants were randomly assigned to canagliflozin or placebo and followed for a mean of 188 weeks. The primary end point for these analyses was adjudicated cardiovascular death or hospitalized HF. RESULTS: Participants with a history of HF at baseline (14.4%) were more frequently women, white, and hypertensive and had a history of prior cardiovascular disease (all P<0.001). Greater proportions of these patients were using therapies such as blockers of the renin angiotensin aldosterone system, diuretics, and β-blockers at baseline (all P<0.001). Overall, cardiovascular death or hospitalized HF was reduced in those treated with canagliflozin compared with placebo (16.3 versus 20.8 per 1000 patient-years; hazard ratio [HR], 0.78; 95% confidence interval [CI], 0.67–0.91), as was fatal or hospitalized HF (HR, 0.70; 95% CI, 0.55–0.89) and hospitalized HF alone (HR, 0.67; 95% CI, 0.52–0.87). The benefit on cardiovascular death or hospitalized HF may be greater in patients with a prior history of HF (HR, 0.61; 95% CI, 0.46–0.80) compared with those without HF at baseline (HR, 0.87; 95% CI, 0.72–1.06; P interaction =0.021). The effects of canagliflozin compared with placebo on other cardiovascular outcomes and key safety outcomes were similar in participants with and without HF at baseline (all interaction P values >0.130), except for a possibly reduced absolute rate of events attributable to osmotic diuresis among those with a prior history of HF (P=0.03). CONCLUSIONS: In patients with type 2 diabetes mellitus and an elevated risk of cardiovascular disease, canagliflozin reduced the risk of cardiovascular death or hospitalized HF across a broad range of different patient subgroups. Benefits may be greater in those with a history of HF at baseline. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01032629 and NCT01989754. Lippincott Williams & Wilkins 2018-07-31 2018-07-30 /pmc/articles/PMC6075881/ /pubmed/29526832 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.034222 Text en © 2018 The Authors. Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited. |
spellingShingle | Original Research Articles Rådholm, Karin Figtree, Gemma Perkovic, Vlado Solomon, Scott D. Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Barrett, Terrance D. Shaw, Wayne Desai, Mehul Matthews, David R. Neal, Bruce Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title | Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title_full | Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title_fullStr | Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title_full_unstemmed | Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title_short | Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program |
title_sort | canagliflozin and heart failure in type 2 diabetes mellitus: results from the canvas program |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075881/ https://www.ncbi.nlm.nih.gov/pubmed/29526832 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.034222 |
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