Updates on cardiovascular outcome trials in diabetes.
Cardiovasc Diabetol · 2017
Last updated 2026-05-28Since 2008, the FDA has required studies to confirm that diabetes medications do not increase heart risks. Trials found that drugs like empagliflozin, semaglutide, and liraglutide not only met safety standards but also lowered heart risks. In 2017, studies on insulin degludec, canagliflozin, exenatide, and acarbose showed no harm to heart health. Earlier trials had already demonstrated similar safety and benefits for other diabetes drugs.
AI summary of the abstract below.
| Journal | Cardiovasc Diabetol, 2017 |
|---|---|
| Citations | 41 |
| Relative citation ratio | 1.50 |
| NIH percentile | 64 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Cardiovascular Risk Reduction |
Abstract
In 2008 the Food and Drug Administration introduced a guidance for industry that requires the investigation of cardiovascular outcomes of glucose-lowering medications. Since then, an increasing number of cardiovascular outcome trials have been completed in diabetes patients with high cardiovascular risk for members of the SGLT-2 and DPP4 inhibitors and GLP-1 receptor agonist classes. The trials confirmed cardiovascular safety for all tested anti-hyperglycaemic drugs and, in addition empagliflozin, semaglutide and liraglutide could even reduce cardiovascular risk. The present review summarizes the results of the DEVOTE, CANVAS, EXSCEL and ACE trials that tested cardiovascular safety of Insulin degludec, canagliflozin, once-weekly exenatide and acarbose and were published in 2017. We provide context on these results by comparing them with earlier trials of glucose-lowering drugs and give an outlook on what to expect in coming years.
Verbatim abstract via PubMed 29020969 ↗