Cardiovascular Outcome Trial Update in Diabetes: New Evidence, Remaining Questions.
Curr Diab Rep · 2017
Last updated 2026-05-28Recent studies show that two GLP-1 drugs—liraglutide and semaglutide—reduced the risk of major heart-related events in people with type 2 diabetes. Another drug, empagliflozin, also lowered this risk and reduced hospital stays for heart failure. These drugs also improved kidney function, but other similar medications did not show the same heart benefits.
AI summary of the abstract below.
| Journal | Curr Diab Rep, 2017 |
|---|---|
| Citations | 3 |
| Relative citation ratio | 0.08 |
| NIH percentile | 7 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Cardiovascular Risk Reduction |
Abstract
PURPOSE OF REVIEW: Seven trials of new agents to treat type 2 diabetes (T2DM) have been performed to assess cardiovascular (CV) safety. A significant amount of information regarding the effects of drugs in three classes is available, with new data from multiple other trials expected shortly. This article provides a summary of recently completed trials.
RECENT FINDINGS: The dipeptidyl peptidase-4 inhibitors studied thus far do not alter the risk of major adverse CV events (MACE). Glucagon like peptide-1 receptor agonists liraglutide and semaglutide, and the sodium glucose cotransporter-2 inhibitor empagliflozin, significantly reduced the risk of MACE. Empagliflozin also decreased the risk of hospitalization for heart failure. Agents demonstrating a CV outcome benefit also improved parameters of renal function. Several newer antihyperglycemic agents have been found to reduce the risk of important CV complications in high-risk patients with T2DM. Future trials are needed to assess the effects of additional drugs and the impact of therapy in lower risk patients and provide additional information regarding non-CV safety outcomes.
Verbatim abstract via PubMed 28726152 ↗