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Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia
Cardiovascular disease (CVD) is the leading cause of death worldwide and is the clinical manifestation of the atherosclerosis. Elevated LDL-cholesterol levels are the first line of therapy but the increasing prevalence in type 2 diabetes mellitus (T2DM) has positioned the cardiometabolic risk as the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826980/ https://www.ncbi.nlm.nih.gov/pubmed/33440821 http://dx.doi.org/10.3390/ijms22020660 |
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author | Aguilar-Ballester, María Hurtado-Genovés, Gema Taberner-Cortés, Alida Herrero-Cervera, Andrea Martínez-Hervás, Sergio González-Navarro, Herminia |
author_facet | Aguilar-Ballester, María Hurtado-Genovés, Gema Taberner-Cortés, Alida Herrero-Cervera, Andrea Martínez-Hervás, Sergio González-Navarro, Herminia |
author_sort | Aguilar-Ballester, María |
collection | PubMed |
description | Cardiovascular disease (CVD) is the leading cause of death worldwide and is the clinical manifestation of the atherosclerosis. Elevated LDL-cholesterol levels are the first line of therapy but the increasing prevalence in type 2 diabetes mellitus (T2DM) has positioned the cardiometabolic risk as the most relevant parameter for treatment. Therefore, the control of this risk, characterized by dyslipidemia, hypertension, obesity, and insulin resistance, has become a major goal in many experimental and clinical studies in the context of CVD. In the present review, we summarized experimental studies and clinical trials of recent anti-diabetic and lipid-lowering therapies targeted to reduce CVD. Specifically, incretin-based therapies, sodium-glucose co-transporter 2 inhibitors, and proprotein convertase subtilisin kexin 9 inactivating therapies are described. Moreover, the novel molecular mechanisms explaining the CVD protection of the drugs reviewed here indicate major effects on vascular cells, inflammatory cells, and cardiomyocytes, beyond their expected anti-diabetic and lipid-lowering control. The revealed key mechanism is a prevention of acute cardiovascular events by restraining atherosclerosis at early stages, with decreased leukocyte adhesion, recruitment, and foam cell formation, and increased plaque stability and diminished necrotic core in advanced plaques. These emergent cardiometabolic therapies have a promising future to reduce CVD burden. |
format | Online Article Text |
id | pubmed-7826980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78269802021-01-25 Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia Aguilar-Ballester, María Hurtado-Genovés, Gema Taberner-Cortés, Alida Herrero-Cervera, Andrea Martínez-Hervás, Sergio González-Navarro, Herminia Int J Mol Sci Review Cardiovascular disease (CVD) is the leading cause of death worldwide and is the clinical manifestation of the atherosclerosis. Elevated LDL-cholesterol levels are the first line of therapy but the increasing prevalence in type 2 diabetes mellitus (T2DM) has positioned the cardiometabolic risk as the most relevant parameter for treatment. Therefore, the control of this risk, characterized by dyslipidemia, hypertension, obesity, and insulin resistance, has become a major goal in many experimental and clinical studies in the context of CVD. In the present review, we summarized experimental studies and clinical trials of recent anti-diabetic and lipid-lowering therapies targeted to reduce CVD. Specifically, incretin-based therapies, sodium-glucose co-transporter 2 inhibitors, and proprotein convertase subtilisin kexin 9 inactivating therapies are described. Moreover, the novel molecular mechanisms explaining the CVD protection of the drugs reviewed here indicate major effects on vascular cells, inflammatory cells, and cardiomyocytes, beyond their expected anti-diabetic and lipid-lowering control. The revealed key mechanism is a prevention of acute cardiovascular events by restraining atherosclerosis at early stages, with decreased leukocyte adhesion, recruitment, and foam cell formation, and increased plaque stability and diminished necrotic core in advanced plaques. These emergent cardiometabolic therapies have a promising future to reduce CVD burden. MDPI 2021-01-11 /pmc/articles/PMC7826980/ /pubmed/33440821 http://dx.doi.org/10.3390/ijms22020660 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Aguilar-Ballester, María Hurtado-Genovés, Gema Taberner-Cortés, Alida Herrero-Cervera, Andrea Martínez-Hervás, Sergio González-Navarro, Herminia Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title | Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title_full | Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title_fullStr | Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title_full_unstemmed | Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title_short | Therapies for the Treatment of Cardiovascular Disease Associated with Type 2 Diabetes and Dyslipidemia |
title_sort | therapies for the treatment of cardiovascular disease associated with type 2 diabetes and dyslipidemia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826980/ https://www.ncbi.nlm.nih.gov/pubmed/33440821 http://dx.doi.org/10.3390/ijms22020660 |
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