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The current landscape for diabetes treatment: Preventing diabetes-associated CV risk.
- Source :
-
Atherosclerosis [Atherosclerosis] 2024 Jul; Vol. 394, pp. 117560. Date of Electronic Publication: 2024 Apr 23. - Publication Year :
- 2024
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Abstract
- Despite the risk of atherosclerosis has progressively declined over the past few decades, subjects with type 2 diabetes mellitus (T2DM) continue to experience substantial excess of atherosclerotic cardiovascular disease (ASCVD)-related events. Therefore, there is urgent need to treat ASCVD disease in T2DM earlier, more intensively, and with greater precision. Many factors concur to increase the risk of atherosclerosis, and multifactorial intervention remains the basis for effective prevention or reduction of atherosclerotic events. The role of anti-hyperglycemic medications in reducing the risk of ASCVD in subjects with T2DM has evolved over the past few years. Multiple cardiovascular outcome trials (CVOTs) with new and emerging glucose-lowering agents, namely SGLT2 inhibitors (SGLT2i) and GLP-1 receptor agonists (GLP1-RA), have demonstrated significant reductions of major cardiovascular events and additional benefits. This robust evidence has changed the landscape for managing people with T2DM. In addition to glycemic and ancillary extra-glycemic properties, SGLT2i and GLP1-RA might exert favorable effects on subclinical and clinical atherosclerosis. Therefore, the objective of this review is to discuss the available evidence supporting anti-atherosclerotic properties of SGLT2i and GLP1-RA, with a quick nod to sotagliflozin and tirzepatide.<br />Competing Interests: Declaration of competing interest Angela Dardano (AD) reported no duality of interest. Cristina Bianchi (CB) reported consulting fees and grants from Lilly, Novo Nordisk, Merck Sharp & Dohme Corp. Monia Garofolo (MG) reported consulting fees from Novo Nordisk, Eli Lilly, Merck Sharp & Dohme Corp. and Bayer Inc. Stefano Del Prato (SDP) has served as president of EASD/European Foundation for the Study of Diabetes (EFSD) (2020–2022); has received research grants to the institution from AstraZeneca and Boehringer Ingelheim; has served as advisor for Abbott, Amarin Corporation, Applied Therapeutics, AstraZeneca, Boehringer Ingelheim, Eli Lilly & Co., EvaPharma, Jiangsu Hengrui Pharmaceuticals Co., Menarini International, Merck Sharpe & Dohme, Novartis Pharmaceutical Co., Novo Nordisk, Sanofi and Sun Pharmaceuticals; and has received fees for speaking from AstraZeneca, Boehringer Ingelheim, Eli Lilly & Co., Laboratori Guidotti, Menarini International, Merck Sharpe & Dohme, and Novo Nordisk. The authors declare that there are no other relationships or activities that might bias, or be perceived to bias, their work.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Humans
Blood Glucose metabolism
Blood Glucose drug effects
Treatment Outcome
Heart Disease Risk Factors
Atherosclerosis prevention & control
Atherosclerosis drug therapy
Risk Assessment
Risk Factors
Incretins therapeutic use
Diabetes Mellitus, Type 2 drug therapy
Diabetes Mellitus, Type 2 complications
Sodium-Glucose Transporter 2 Inhibitors therapeutic use
Hypoglycemic Agents therapeutic use
Glucagon-Like Peptide-1 Receptor agonists
Cardiovascular Diseases prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1484
- Volume :
- 394
- Database :
- MEDLINE
- Journal :
- Atherosclerosis
- Publication Type :
- Academic Journal
- Accession number :
- 38688748
- Full Text :
- https://doi.org/10.1016/j.atherosclerosis.2024.117560