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Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program
BACKGROUND: Canagliflozin is approved for glucose lowering in type 2 diabetes and confers cardiovascular and renal benefits. We sought to assess whether it had benefits in people with chronic kidney disease, including those with an estimated glomerular filtration rate (eGFR) between 30 and 45 mL/min...
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/PMC6181277/ https://www.ncbi.nlm.nih.gov/pubmed/29941478 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.035901 |
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author | Neuen, Brendon L. Ohkuma, Toshiaki Neal, Bruce Matthews, David R. de Zeeuw, Dick Mahaffey, Kenneth W. Fulcher, Greg Desai, Mehul Li, Qiang Deng, Hsiaowei Rosenthal, Norm Jardine, Meg J. Bakris, George Perkovic, Vlado |
author_facet | Neuen, Brendon L. Ohkuma, Toshiaki Neal, Bruce Matthews, David R. de Zeeuw, Dick Mahaffey, Kenneth W. Fulcher, Greg Desai, Mehul Li, Qiang Deng, Hsiaowei Rosenthal, Norm Jardine, Meg J. Bakris, George Perkovic, Vlado |
author_sort | Neuen, Brendon L. |
collection | PubMed |
description | BACKGROUND: Canagliflozin is approved for glucose lowering in type 2 diabetes and confers cardiovascular and renal benefits. We sought to assess whether it had benefits in people with chronic kidney disease, including those with an estimated glomerular filtration rate (eGFR) between 30 and 45 mL/min/1.73 m(2) in whom the drug is not currently approved for use. METHODS: The CANVAS Program randomized 10 142 participants with type 2 diabetes and eGFR >30 mL/min/1.73 m(2) to canagliflozin or placebo. The primary outcome was a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke, with other cardiovascular, renal, and safety outcomes. This secondary analysis describes outcomes in participants with and without chronic kidney disease, defined as eGFR <60 and ≥60 mL/min/1.73 m(2), and according to baseline kidney function (eGFR <45, 45 to <60, 60 to <90, and ≥90 mL/min/1.73 m(2)). RESULTS: At baseline, 2039 (20.1%) participants had an eGFR <60 mL/min/1.73 m(2), 71.6% of whom had a history of cardiovascular disease. The effect of canagliflozin on the primary outcome was similar in people with chronic kidney disease (hazard ratio, 0.70; 95% CI, 0.55–0.90) and those with preserved kidney function (hazard ratio, 0.92; 95% CI, 0.79–1.07; P heterogeneity = 0.08). Relative effects on most cardiovascular and renal outcomes were similar across eGFR subgroups, with possible heterogeneity suggested only for the outcome of fatal/nonfatal stroke (P heterogeneity = 0.01), as were results for almost all safety outcomes. CONCLUSIONS: The effects of canagliflozin on cardiovascular and renal outcomes were not modified by baseline level of kidney function in people with type 2 diabetes and a history or high risk of cardiovascular disease down to eGFR levels of 30 mL/min/1.73 m(2). Reassessing current limitations on the use of canagliflozin in chronic kidney disease may allow additional individuals to benefit from this therapy. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01032629, NCT01989754. |
format | Online Article Text |
id | pubmed-6181277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-61812772018-10-25 Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program Neuen, Brendon L. Ohkuma, Toshiaki Neal, Bruce Matthews, David R. de Zeeuw, Dick Mahaffey, Kenneth W. Fulcher, Greg Desai, Mehul Li, Qiang Deng, Hsiaowei Rosenthal, Norm Jardine, Meg J. Bakris, George Perkovic, Vlado Circulation Original Research Articles BACKGROUND: Canagliflozin is approved for glucose lowering in type 2 diabetes and confers cardiovascular and renal benefits. We sought to assess whether it had benefits in people with chronic kidney disease, including those with an estimated glomerular filtration rate (eGFR) between 30 and 45 mL/min/1.73 m(2) in whom the drug is not currently approved for use. METHODS: The CANVAS Program randomized 10 142 participants with type 2 diabetes and eGFR >30 mL/min/1.73 m(2) to canagliflozin or placebo. The primary outcome was a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke, with other cardiovascular, renal, and safety outcomes. This secondary analysis describes outcomes in participants with and without chronic kidney disease, defined as eGFR <60 and ≥60 mL/min/1.73 m(2), and according to baseline kidney function (eGFR <45, 45 to <60, 60 to <90, and ≥90 mL/min/1.73 m(2)). RESULTS: At baseline, 2039 (20.1%) participants had an eGFR <60 mL/min/1.73 m(2), 71.6% of whom had a history of cardiovascular disease. The effect of canagliflozin on the primary outcome was similar in people with chronic kidney disease (hazard ratio, 0.70; 95% CI, 0.55–0.90) and those with preserved kidney function (hazard ratio, 0.92; 95% CI, 0.79–1.07; P heterogeneity = 0.08). Relative effects on most cardiovascular and renal outcomes were similar across eGFR subgroups, with possible heterogeneity suggested only for the outcome of fatal/nonfatal stroke (P heterogeneity = 0.01), as were results for almost all safety outcomes. CONCLUSIONS: The effects of canagliflozin on cardiovascular and renal outcomes were not modified by baseline level of kidney function in people with type 2 diabetes and a history or high risk of cardiovascular disease down to eGFR levels of 30 mL/min/1.73 m(2). Reassessing current limitations on the use of canagliflozin in chronic kidney disease may allow additional individuals to benefit from this therapy. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01032629, NCT01989754. Lippincott Williams & Wilkins 2018-10-09 2018-10-08 /pmc/articles/PMC6181277/ /pubmed/29941478 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.035901 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 Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made. |
spellingShingle | Original Research Articles Neuen, Brendon L. Ohkuma, Toshiaki Neal, Bruce Matthews, David R. de Zeeuw, Dick Mahaffey, Kenneth W. Fulcher, Greg Desai, Mehul Li, Qiang Deng, Hsiaowei Rosenthal, Norm Jardine, Meg J. Bakris, George Perkovic, Vlado Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title | Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title_full | Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title_fullStr | Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title_full_unstemmed | Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title_short | Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data From the CANVAS Program |
title_sort | cardiovascular and renal outcomes with canagliflozin according to baseline kidney function: data from the canvas program |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181277/ https://www.ncbi.nlm.nih.gov/pubmed/29941478 http://dx.doi.org/10.1161/CIRCULATIONAHA.118.035901 |
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