Cardiovascular Outcomes of New Medications for Type 2 Diabetes.
Diabetes Technol Ther · 2016
Last updated 2026-05-28Seven clinical trials tested new diabetes medications for their effects on heart health. Three trials showed that the GLP-1 drugs liraglutide and semaglutide reduced major heart events—like heart attacks and strokes—by 12% and 26% respectively, compared to a placebo. One trial found that saxagliptin increased hospitalizations for heart failure. The studies used different patient groups and designs, so their results should be compared carefully.
AI summary of the abstract below.
| Journal | Diabetes Technol Ther, 2016 |
|---|---|
| Citations | 6 |
| Relative citation ratio | 0.21 |
| NIH percentile | 14 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Cardiovascular Risk Reduction |
Abstract
Cardiovascular (CV) disease remains the leading cause of death in people with diabetes, highlighting the importance of using treatment options that do not increase CV risk or possibly decrease CV outcomes. Since 2008, the Food and Drug Administration has required demonstration of CV safety for all new medications developed for the glycemic management of diabetes. Seven trials have been published that have established CV safety for three DPP-4 inhibitors (alogliptin, saxagliptin, and sitagliptin), three GLP-1 receptor agonists (liraglutide, lixisenatide, and semaglutide), and one sodium-glucose cotransporter-2 inhibitor (empagliflozin). Three of those studies also established superiority with liraglutide, empagliflozin, and semaglutide at reducing the composite primary endpoint of major CV events (CV death, nonfatal myocardial infarction, and nonfatal stroke). In addition, one trial found an increase in heart failure hospitalizations with saxagliptin. The findings of these trials must be compared and contrasted cautiously given the differences in patient populations and trial designs, but together they provide important information that can be used to shape our treatment guideline recommendations and patient-specific treatment decisions.
Verbatim abstract via PubMed 27835045 ↗