Longer acting GLP-1 receptor agonists and the potential for improved cardiovascular outcomes: a review of current literature.
Expert Rev Endocrinol Metab · 2013
Last updated 2026-05-28Longer-acting GLP-1 drugs like once-weekly exenatide, dulaglutide, albiglutide, semaglutide, and ITCA650 reduce blood sugar control (A1c) and weight as well or better than the twice-daily version of exenatide. These longer-acting options also cause less nausea and require fewer injections. Early research suggests they may improve heart-related measures, some of which are not linked to weight or blood sugar changes.
AI summary of the abstract below.
| Journal | Expert Rev Endocrinol Metab, 2013 |
|---|---|
| Citations | 18 |
| Relative citation ratio | 0.55 |
| NIH percentile | 32 |
| Molecules | — |
| Conditions studied | Cardiovascular Risk Reduction |
Abstract
With the rapidly rising incidence of Type 2 diabetes and an increasing variety of medications available for treatment, choosing the ideal regimen for patients can be challenging. Longer-acting glucagon-like peptide-1 (GLP-1) receptor agonists and devices have been recently developed and include once-weekly exenatide, dulaglutide, albiglutide, semaglutide and miniosmotic pump ITCA650. Some of the attractive qualities of the GLP-1 receptor agonist class include its association with weightloss and potential for cardiovascular benefits. The longer-acting forms have been shown in several studies to produce equal or greater reduction in A1c and weight compared with the standard twice-daily formulation of exenatide. They also result in lower reported incidence of nausea, in the setting of a less frequent injection schedule that would be desirable to many diabetic patients. There are emerging data to suggest patients treated with longer-acting GLP-1 receptor agonists have improved cardiac parameters, some of which are independent of weight and A1c reductions.
Verbatim abstract via PubMed 30780817 ↗