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Repurposing Antidiabetic Drugs for Cardiovascular Disease
Metabolic diseases and diabetes represent an increasing global challenge for human health care. As associated with a strongly elevated risk of developing atherosclerosis, kidney failure and death from myocardial infarction or stroke, the treatment of diabetes requires a more effective approach than...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522553/ https://www.ncbi.nlm.nih.gov/pubmed/33041865 http://dx.doi.org/10.3389/fphys.2020.568632 |
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author | Schubert, Mario Hansen, Sinah Leefmann, Julian Guan, Kaomei |
author_facet | Schubert, Mario Hansen, Sinah Leefmann, Julian Guan, Kaomei |
author_sort | Schubert, Mario |
collection | PubMed |
description | Metabolic diseases and diabetes represent an increasing global challenge for human health care. As associated with a strongly elevated risk of developing atherosclerosis, kidney failure and death from myocardial infarction or stroke, the treatment of diabetes requires a more effective approach than lowering blood glucose levels. This review summarizes the evidence for the cardioprotective benefits induced by antidiabetic agents, including sodium-glucose cotransporter 2 inhibitor (SGLT2i) and glucagon-like peptide-1 receptor agonist (GLP1-RA), along with sometimes conversely discussed effects of dipeptidyl peptidase-4 inhibitor (DPP4i) and metformin in patients with high cardiovascular risk with or without type 2 diabetes. Moreover, the proposed mechanisms of the different drugs are described based on the results of preclinical studies. Recent cardiovascular outcome trials unexpectedly confirmed a beneficial effect of GLP-1RA and SGLT2i in type 2 diabetes patients with high cardiovascular risk and with standard care, which was independent of glycaemic control. These results triggered a plethora of studies to clarify the underlying mechanisms and the relevance of these effects. Taken together, the available data strongly highlight the potential of repurposing the original antidiabetics GLP1-RA and SGLT2i to improve cardiovascular outcome even in non-diabetic patients with cardiovascular diseases. |
format | Online Article Text |
id | pubmed-7522553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75225532020-10-09 Repurposing Antidiabetic Drugs for Cardiovascular Disease Schubert, Mario Hansen, Sinah Leefmann, Julian Guan, Kaomei Front Physiol Physiology Metabolic diseases and diabetes represent an increasing global challenge for human health care. As associated with a strongly elevated risk of developing atherosclerosis, kidney failure and death from myocardial infarction or stroke, the treatment of diabetes requires a more effective approach than lowering blood glucose levels. This review summarizes the evidence for the cardioprotective benefits induced by antidiabetic agents, including sodium-glucose cotransporter 2 inhibitor (SGLT2i) and glucagon-like peptide-1 receptor agonist (GLP1-RA), along with sometimes conversely discussed effects of dipeptidyl peptidase-4 inhibitor (DPP4i) and metformin in patients with high cardiovascular risk with or without type 2 diabetes. Moreover, the proposed mechanisms of the different drugs are described based on the results of preclinical studies. Recent cardiovascular outcome trials unexpectedly confirmed a beneficial effect of GLP-1RA and SGLT2i in type 2 diabetes patients with high cardiovascular risk and with standard care, which was independent of glycaemic control. These results triggered a plethora of studies to clarify the underlying mechanisms and the relevance of these effects. Taken together, the available data strongly highlight the potential of repurposing the original antidiabetics GLP1-RA and SGLT2i to improve cardiovascular outcome even in non-diabetic patients with cardiovascular diseases. Frontiers Media S.A. 2020-09-15 /pmc/articles/PMC7522553/ /pubmed/33041865 http://dx.doi.org/10.3389/fphys.2020.568632 Text en Copyright © 2020 Schubert, Hansen, Leefmann and Guan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Schubert, Mario Hansen, Sinah Leefmann, Julian Guan, Kaomei Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title | Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title_full | Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title_fullStr | Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title_full_unstemmed | Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title_short | Repurposing Antidiabetic Drugs for Cardiovascular Disease |
title_sort | repurposing antidiabetic drugs for cardiovascular disease |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522553/ https://www.ncbi.nlm.nih.gov/pubmed/33041865 http://dx.doi.org/10.3389/fphys.2020.568632 |
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