[Effects of glucagon-like peptide-1 receptor agonists on cardiovascular risk factors and the cardiovascular system].
G Ital Cardiol (Rome) · 2016
Last updated 2026-05-28In people with type 2 diabetes, the GLP-1 drug liraglutide reduced serious cardiovascular events after 24 months of treatment, while the SGLT2 drug empagliflozin did so within 3 months. The exact reasons for these benefits are not yet clear, but researchers suggest liraglutide may work by changing plaque in arteries, while empagliflozin’s effects may relate to shifts in how the body uses energy.
AI summary of the abstract below.
| Journal | G Ital Cardiol (Rome), 2016 |
|---|---|
| Citations | 1 |
| Relative citation ratio | 0.02 |
| NIH percentile | 4 |
| Molecules | — |
| Conditions studied | Cardiovascular Risk Reduction |
Abstract
The results of the cardiovascular outcome trials comparing the SGLT2 inhibitor empagliflozin and the glucagon-like peptide-1 receptor agonist liraglutide to placebo have been recently published. Interestingly, empagliflozin and liraglutide treatments significantly reduce cardiovascular events in subjects with type 2 diabetes. The mechanisms underlying the observed cardioprotective effects of empagliflozin and liraglutide are speculative and future studies are needed to better understand these results. However, since reduction in the primary outcome was evident 3 months after starting empagliflozin and 24 months after starting liraglutide, it is tempting to hypothesize that the cardiovascular benefits observed in diabetic patients treated with empagliflozin are due to its hemodynamic effects and to metabolic substrate shift induced by the mild and persistent hyperketonemia, while the positive effects of liraglutide treatment may be attributable to biologic changes of atherosclerotic lesions.
Verbatim abstract via PubMed 28151517 ↗