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The Role of Glucagon-Like Peptide 1 Receptor Agonists and Sodium-Glucose Cotransporter 2 Inhibitors in Reducing Cardiovascular Events in Patients with Type 2 Diabetes.

Endocrinol Metab (Seoul) · 2019

Last updated 2026-07-15

Research shows that GLP-1 receptor agonists and SGLT-2 inhibitors, like semaglutide, liraglutide, empagliflozin, and canagliflozin, may help reduce heart disease risks in people with type 2 diabetes. These drugs were studied in clinical trials and found to be safe while offering protective effects against cardiovascular disease.

AI summary of the abstract below.

JournalEndocrinol Metab (Seoul), 2019
Citations16
Relative citation ratio0.77
NIH percentile42
Molecules

Abstract

The prevalence of type 2 diabetes mellitus (T2DM), which is associated with cardiovascular morbidity and mortality, is increasing worldwide. Although there have been advances in diabetes treatments that reduce microvascular complications (nephropathy, neuropathy, retinopathy), many clinical studies have found that conventional oral hypoglycemic agents and glucose control alone failed to reduce cardiovascular disease. Thus, incretin-based therapies including glucagon-like peptide 1 (GLP-1) receptor agonists (RAs) and sodium-glucose cotransporter 2 inhibitors (SGLT-2Is) represent a new area of research, and may serve as novel therapeutics for treating hyperglycemia and modifying other cardiovascular risk factors. Recently, it has been confirmed that several drugs in these classes, including canagliflozin, empagliflozin, semaglutide, and liraglutide, are safe and possess cardioprotective effects. We review the most recent cardiovascular outcome trials on GLP-1RAs and SGLT-2Is, and discuss their implications for treating patients with T2DM in terms of protective effects against cardiovascular disease.

Verbatim abstract via PubMed 31099200 ↗