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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
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.
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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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