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Diabetes: how to manage cardiovascular risk in secondary prevention patients

Atherosclerotic cardiovascular disease (ASCVD) commonly affects people with type 2 diabetes (T2D). Historically, traditional cardiovascular (CV) risk-lowering therapies in patients with T2D and ASCVD have included antiplatelet agents, blood pressure-lowering therapies, lipid-lowering therapies and h...

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Detalles Bibliográficos
Autores principales: Anderson, Sarah L, Marrs, Joel C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205572/
https://www.ncbi.nlm.nih.gov/pubmed/35775074
http://dx.doi.org/10.7573/dic.2021-10-1
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author Anderson, Sarah L
Marrs, Joel C
author_facet Anderson, Sarah L
Marrs, Joel C
author_sort Anderson, Sarah L
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description Atherosclerotic cardiovascular disease (ASCVD) commonly affects people with type 2 diabetes (T2D). Historically, traditional cardiovascular (CV) risk-lowering therapies in patients with T2D and ASCVD have included antiplatelet agents, blood pressure-lowering therapies, lipid-lowering therapies and healthy lifestyle modifications. In the past decade, multiple antihyperglycaemic agents have emerged as CV risk-lowering therapies in this population as well. This article provides a narrative review on the current non-glycaemic and glycaemic treatment options for CV risk reduction in patients with T2D and ASCVD. The FDA requirement that all new antihyperglycaemic agents undergo cardiovascular outcomes trials has demonstrated increasing evidence to support the role of glucagon-like peptide 1 (GLP1) receptor agonists and sodium–glucose cotransporter 2 (SGLT2) inhibitors as first-line agents for both glycaemic control and CV risk reduction in this population.
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spelling pubmed-92055722022-06-29 Diabetes: how to manage cardiovascular risk in secondary prevention patients Anderson, Sarah L Marrs, Joel C Drugs Context Review Atherosclerotic cardiovascular disease (ASCVD) commonly affects people with type 2 diabetes (T2D). Historically, traditional cardiovascular (CV) risk-lowering therapies in patients with T2D and ASCVD have included antiplatelet agents, blood pressure-lowering therapies, lipid-lowering therapies and healthy lifestyle modifications. In the past decade, multiple antihyperglycaemic agents have emerged as CV risk-lowering therapies in this population as well. This article provides a narrative review on the current non-glycaemic and glycaemic treatment options for CV risk reduction in patients with T2D and ASCVD. The FDA requirement that all new antihyperglycaemic agents undergo cardiovascular outcomes trials has demonstrated increasing evidence to support the role of glucagon-like peptide 1 (GLP1) receptor agonists and sodium–glucose cotransporter 2 (SGLT2) inhibitors as first-line agents for both glycaemic control and CV risk reduction in this population. BioExcel Publishing Ltd 2022-06-14 /pmc/articles/PMC9205572/ /pubmed/35775074 http://dx.doi.org/10.7573/dic.2021-10-1 Text en Copyright © 2022 Anderson SL, Marrs JC https://creativecommons.org/licenses/by-nc-nd/4.0/Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Review
Anderson, Sarah L
Marrs, Joel C
Diabetes: how to manage cardiovascular risk in secondary prevention patients
title Diabetes: how to manage cardiovascular risk in secondary prevention patients
title_full Diabetes: how to manage cardiovascular risk in secondary prevention patients
title_fullStr Diabetes: how to manage cardiovascular risk in secondary prevention patients
title_full_unstemmed Diabetes: how to manage cardiovascular risk in secondary prevention patients
title_short Diabetes: how to manage cardiovascular risk in secondary prevention patients
title_sort diabetes: how to manage cardiovascular risk in secondary prevention patients
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205572/
https://www.ncbi.nlm.nih.gov/pubmed/35775074
http://dx.doi.org/10.7573/dic.2021-10-1
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