Safety and cardiometabolic efficacy of novel antidiabetic drugs

• Published in: Expert opinion on drug safety Vol. 22; no. 2; p. 119
• Main Authors: Michaud, Liana, Seplowe, Matthew, Meir, Juliet, Aronow, Wilbert S
• Format: Journal Article
• Language: English
• Published: England 01.02.2023
• Subjects: Arrhythmias, Cardiac - drug therapy; Cardiometabolic Risk Factors; Dipeptidyl-Peptidase IV Inhibitors - adverse effects; Dipeptidyl-Peptidase IV Inhibitors - therapeutic use; Glucagon-Like Peptide-1 Receptor - agonists; Heart Failure - drug therapy; Hospitalization; Humans; Hypoglycemic Agents - adverse effects; Hypoglycemic Agents - therapeutic use; Myocardial Infarction - drug therapy; Randomized Controlled Trials as Topic; Sodium-Glucose Transporter 2 Inhibitors - adverse effects; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use; dipeptidyl dipeptidase-4 inhibitors; cardiovascular outcome trials; type 2 diabetes; Cardiovascular safety; sodium-glucose cotransporter-2 inhibitors; glucagon-like peptide-1 receptor agonists; novel antidiabetic drugs
• ISSN: 1744-764X
• DOI: 10.1080/14740338.2023.2188190

There are three major drug classes discussed in this review: dipeptidyl dipeptidase-4 (DPP4) inhibitors, glucagon-like peptide-1 receptor agonists (GLP-1 RAS), and sodium-glucose cotransporter-2 (SGLT2) inhibitors. A literature review of the landmark cardiovascular outcome trials from 2008 to 2021 was conducted. The cumulative data shown in this review suggest that in patients with Type 2 Diabetes (T2D), SGLT2 inhibitors and GLP-1 RAS may reduce cardiovascular (CV) risk. Specifically, in the heart failure (HF) population, SGLT2 inhibitors have shown a reduction in hospitalizations in some randomized controlled trials (RCTs). DPP4 inhibitors have not shown a similar reduction in CV risk and even exhibited an increase in hospitalizations for HF in one RCT. It is important to note that the DPP4 inhibitors did not demonstrate an increase in major CV events, with the exception of the increase in HF hospitalizations in the SAVOR TIMI 53 trial. Future avenues of research to explore include the use of novel antidiabetic agents to reduce post-myocardial infarction (MI) CV risk and arrhythmias independent of their use as diabetic agents.