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Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy
Dapagliflozin is a selective sodium–glucose cotransporter 2 inhibitor (SGLT2i) indicated for the treatment of type 2 diabetes mellitus (T2DM), heart failure with reduced ejection fraction and chronic kidney disease. In all indications, treatment can be initiated in adults with estimated glomerular f...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240142/ https://www.ncbi.nlm.nih.gov/pubmed/35687260 http://dx.doi.org/10.1007/s13300-022-01280-6 |
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author | González-Clemente, José M. García-Castillo, María Gorgojo-Martínez, Juan J. Jiménez, Alberto Llorente, Ignacio Matute, Eduardo Tejera, Cristina Izarra, Aitziber Lecube, Albert |
author_facet | González-Clemente, José M. García-Castillo, María Gorgojo-Martínez, Juan J. Jiménez, Alberto Llorente, Ignacio Matute, Eduardo Tejera, Cristina Izarra, Aitziber Lecube, Albert |
author_sort | González-Clemente, José M. |
collection | PubMed |
description | Dapagliflozin is a selective sodium–glucose cotransporter 2 inhibitor (SGLT2i) indicated for the treatment of type 2 diabetes mellitus (T2DM), heart failure with reduced ejection fraction and chronic kidney disease. In all indications, treatment can be initiated in adults with estimated glomerular filtration rate of at least 25 mL/min/1.73 m(2). As monotherapy or as an additive therapy, dapagliflozin has been shown to promote better glycaemic control, associated with a reduction in body weight and blood pressure in a wide range of patients. In addition, dapagliflozin has a positive impact on arterial stiffness, helps to control the lipid profile and contributes to a reduced risk of cardiovascular complications. This article reviews the current scientific evidence on the role of dapagliflozin in cardiovascular risk factors including arterial stiffness, cardiovascular disease and heart failure in patients with T2DM, with the aim of helping to translate this evidence into clinical practice. The underuse of SGLT2i in actual clinical practice is also discussed. |
format | Online Article Text |
id | pubmed-9240142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-92401422022-06-30 Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy González-Clemente, José M. García-Castillo, María Gorgojo-Martínez, Juan J. Jiménez, Alberto Llorente, Ignacio Matute, Eduardo Tejera, Cristina Izarra, Aitziber Lecube, Albert Diabetes Ther Review Dapagliflozin is a selective sodium–glucose cotransporter 2 inhibitor (SGLT2i) indicated for the treatment of type 2 diabetes mellitus (T2DM), heart failure with reduced ejection fraction and chronic kidney disease. In all indications, treatment can be initiated in adults with estimated glomerular filtration rate of at least 25 mL/min/1.73 m(2). As monotherapy or as an additive therapy, dapagliflozin has been shown to promote better glycaemic control, associated with a reduction in body weight and blood pressure in a wide range of patients. In addition, dapagliflozin has a positive impact on arterial stiffness, helps to control the lipid profile and contributes to a reduced risk of cardiovascular complications. This article reviews the current scientific evidence on the role of dapagliflozin in cardiovascular risk factors including arterial stiffness, cardiovascular disease and heart failure in patients with T2DM, with the aim of helping to translate this evidence into clinical practice. The underuse of SGLT2i in actual clinical practice is also discussed. Springer Healthcare 2022-06-10 2022-07 /pmc/articles/PMC9240142/ /pubmed/35687260 http://dx.doi.org/10.1007/s13300-022-01280-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review González-Clemente, José M. García-Castillo, María Gorgojo-Martínez, Juan J. Jiménez, Alberto Llorente, Ignacio Matute, Eduardo Tejera, Cristina Izarra, Aitziber Lecube, Albert Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title | Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title_full | Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title_fullStr | Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title_full_unstemmed | Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title_short | Beyond the Glycaemic Control of Dapagliflozin: Impact on Arterial Stiffness and Macroangiopathy |
title_sort | beyond the glycaemic control of dapagliflozin: impact on arterial stiffness and macroangiopathy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240142/ https://www.ncbi.nlm.nih.gov/pubmed/35687260 http://dx.doi.org/10.1007/s13300-022-01280-6 |
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