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Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program
AIMS/HYPOTHESIS: The primary analysis of the Canagliflozin cardioVascular Assessment Study (CANVAS) Program showed canagliflozin to have a beneficial effect on cardiovascular and renal outcomes in people with type 2 diabetes at high cardiovascular risk, but also an unexpected increased risk of major...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509073/ https://www.ncbi.nlm.nih.gov/pubmed/30868176 http://dx.doi.org/10.1007/s00125-019-4839-8 |
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author | Matthews, David R. Li, Qiang Perkovic, Vlado Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Desai, Mehul Hiatt, William R. Nehler, Mark Fabbrini, Elisa Kavalam, Mary Lee, Mary Neal, Bruce |
author_facet | Matthews, David R. Li, Qiang Perkovic, Vlado Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Desai, Mehul Hiatt, William R. Nehler, Mark Fabbrini, Elisa Kavalam, Mary Lee, Mary Neal, Bruce |
author_sort | Matthews, David R. |
collection | PubMed |
description | AIMS/HYPOTHESIS: The primary analysis of the Canagliflozin cardioVascular Assessment Study (CANVAS) Program showed canagliflozin to have a beneficial effect on cardiovascular and renal outcomes in people with type 2 diabetes at high cardiovascular risk, but also an unexpected increased risk of major or minor lower extremity amputation. These secondary analyses explore this finding in more detail. METHODS: The effect of canagliflozin on amputation risk in the CANVAS Program was calculated for amputations of different types and proximate aetiologies and different canagliflozin doses. Univariate and multivariate associations of baseline characteristics with amputation risk were determined and proportional and absolute effects of canagliflozin were compared across subgroups. RESULTS: There were 187 (1.8%) participants with atraumatic lower extremity amputations (minor 71%, major 29%); as previously published, rates were 6.30 vs 3.37 per 1000 participant-years with canagliflozin vs placebo (HR 1.97 [95% CI 1.41, 2.75]). Risk was similar for ischaemic and infective aetiologies and for 100 mg and 300 mg doses. Overall amputation risk was strongly associated with baseline history of prior amputation (major or minor) (HR 21.31 [95% CI 15.40, 29.49]) and other established risk factors. No interactions between randomised treatment and participant characteristics explained the effect of canagliflozin on amputation risk. For every clinical subgroup studied, numbers of amputation events projected were smaller than numbers of major adverse cardiovascular events averted. CONCLUSIONS/INTERPRETATION: The CANVAS Program demonstrated that canagliflozin increased the risk of amputation (mainly minor) in this study population. Anticipated risk factors for amputation were identified, such as prior history of amputation, peripheral vascular disease and neuropathy, but no specific aetiological mechanism or at-risk subgroup for canagliflozin was identified. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00125-019-4839-8) contains peer-reviewed but unedited supplementary material, which is available to authorised users. |
format | Online Article Text |
id | pubmed-6509073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-65090732019-05-28 Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program Matthews, David R. Li, Qiang Perkovic, Vlado Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Desai, Mehul Hiatt, William R. Nehler, Mark Fabbrini, Elisa Kavalam, Mary Lee, Mary Neal, Bruce Diabetologia Article AIMS/HYPOTHESIS: The primary analysis of the Canagliflozin cardioVascular Assessment Study (CANVAS) Program showed canagliflozin to have a beneficial effect on cardiovascular and renal outcomes in people with type 2 diabetes at high cardiovascular risk, but also an unexpected increased risk of major or minor lower extremity amputation. These secondary analyses explore this finding in more detail. METHODS: The effect of canagliflozin on amputation risk in the CANVAS Program was calculated for amputations of different types and proximate aetiologies and different canagliflozin doses. Univariate and multivariate associations of baseline characteristics with amputation risk were determined and proportional and absolute effects of canagliflozin were compared across subgroups. RESULTS: There were 187 (1.8%) participants with atraumatic lower extremity amputations (minor 71%, major 29%); as previously published, rates were 6.30 vs 3.37 per 1000 participant-years with canagliflozin vs placebo (HR 1.97 [95% CI 1.41, 2.75]). Risk was similar for ischaemic and infective aetiologies and for 100 mg and 300 mg doses. Overall amputation risk was strongly associated with baseline history of prior amputation (major or minor) (HR 21.31 [95% CI 15.40, 29.49]) and other established risk factors. No interactions between randomised treatment and participant characteristics explained the effect of canagliflozin on amputation risk. For every clinical subgroup studied, numbers of amputation events projected were smaller than numbers of major adverse cardiovascular events averted. CONCLUSIONS/INTERPRETATION: The CANVAS Program demonstrated that canagliflozin increased the risk of amputation (mainly minor) in this study population. Anticipated risk factors for amputation were identified, such as prior history of amputation, peripheral vascular disease and neuropathy, but no specific aetiological mechanism or at-risk subgroup for canagliflozin was identified. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00125-019-4839-8) contains peer-reviewed but unedited supplementary material, which is available to authorised users. Springer Berlin Heidelberg 2019-03-12 2019 /pmc/articles/PMC6509073/ /pubmed/30868176 http://dx.doi.org/10.1007/s00125-019-4839-8 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Matthews, David R. Li, Qiang Perkovic, Vlado Mahaffey, Kenneth W. de Zeeuw, Dick Fulcher, Greg Desai, Mehul Hiatt, William R. Nehler, Mark Fabbrini, Elisa Kavalam, Mary Lee, Mary Neal, Bruce Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title | Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title_full | Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title_fullStr | Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title_full_unstemmed | Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title_short | Effects of canagliflozin on amputation risk in type 2 diabetes: the CANVAS Program |
title_sort | effects of canagliflozin on amputation risk in type 2 diabetes: the canvas program |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509073/ https://www.ncbi.nlm.nih.gov/pubmed/30868176 http://dx.doi.org/10.1007/s00125-019-4839-8 |
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