Study of postprandial lipaemia in type 2 diabetes mellitus: exenatide versus liraglutide.
J Diabetes Res · 2014
Last updated 2026-05-28In a 2-week study of 20 people with type 2 diabetes, two GLP-1 drugs—liraglutide and exenatide—were compared for their effects on blood fat levels after a meal. Both drugs lowered post-meal blood fats equally after the first dose and again after two weeks of treatment, though researchers noted the exact way this happens is still unclear.
AI summary of the abstract below.
| Journal | J Diabetes Res, 2014 |
|---|---|
| Citations | 20 |
| Relative citation ratio | 0.66 |
| NIH percentile | 37 |
| Molecules | liraglutide, exenatide |
| Conditions studied | Type 2 Diabetes |
Abstract
Therapeutic approaches based on the actions of the incretin hormone GLP-1 have been widely established in the management of T2DM. Nevertheless, much less research has been aimed at elucidating the role of GLP-1 in lipid metabolism and in particular postprandial dyslipidemia. Exenatide and liraglutide are two GLP-1 receptor agonists which are currently available as subcutaneously administered treatment for T2DM but their chronic effects on postprandial lipaemia have not been well investigated. The aim of this study is to examine the effect of treatment with either liraglutide or exenatide for two weeks on postprandial lipaemia in obese subjects with T2DM. This study was a single-center, two-armed, randomized, controlled 2-week prospective intervention trial in 20 subjects with T2DM. Patients were randomized to receive either liraglutide or exenatide treatment and underwent a standardized meal tolerance test early in the morning after 10 h fast at baseline (visit 1, beginning of treatment) and after a two-week treatment period (visit 2). Exenatide and liraglutide both appear to be equally effective in lowering postprandial lipaemia after the first administration and after a two-week treatment. The mechanisms which lead to this phenomenon, which seem to be independent of gastric emptying, are yet to be studied.
Verbatim abstract via PubMed 25165723 ↗
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