Weight beneficial treatments for type 2 diabetes.
J Clin Endocrinol Metab · 2011
Last updated 2026-05-28Research shows that metformin and newer drugs like GLP-1 agonists help with weight loss in people with type 2 diabetes, while DPP-4 inhibitors and bile acid sequestrants have no effect on weight. Among GLP-1 drugs, liraglutide and exenatide both aid weight loss, but liraglutide may improve blood sugar control more than exenatide when used as a second treatment. Insulin detemir is linked to less weight gain compared to other insulins.
AI summary of the abstract below.
| Journal | J Clin Endocrinol Metab, 2011 |
|---|---|
| Citations | 64 |
| Relative citation ratio | 1.94 |
| NIH percentile | 73 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
CONTEXT: The close link between type 2 diabetes and excess body weight highlights the need to consider the weight effects of different treatment regimens. We examine the impact of "weight-friendly" type 2 diabetes pharmacotherapies and suggest treatment strategies that mitigate weight gain.
EVIDENCE ACQUISITION: Evidence was identified via PubMed search by class and agent and in bibliographies of review articles, with final articles for inclusion selected by author consensus.
EVIDENCE SYNTHESIS: Substantial evidence confirms the weight benefits of metformin and shows that, of the newer available agents, glucagon-like peptide-1 (GLP-1) agonists and amylin analogs promote weight loss. Dipeptidyl peptidase-4 (DPP-4) inhibitors and bile acid sequestrants are weight-neutral. Liraglutide and exenatide appear to have similar effects on weight; however, recent research suggests a potentially greater effect of liraglutide on glycemic control compared to exenatide, when used as a second-line therapy. Mounting evidence suggests that insulin detemir may provide the most favorable weight benefits of available insulins.
CONCLUSIONS: Weight-beneficial agents should be considered in patients, particularly obese patients, who fail to reach glycemic targets on metformin therapy. We propose the following treatment choices based on potential weight benefit and blood glucose increment: long-acting GLP-1 agonists (liraglutide), DPP-4 inhibitors, bile acid sequestrants, amylin analogs, and basal insulin for patients with elevated fasting plasma glucose; and short-acting (exenatide) or long-acting GLP-1 agonists, amylin analogs, DPP-4 inhibitors, acarbose, and bile acid sequestrants for patients with elevated postprandial glucose. The weight-sparing effects of insulin detemir, notably in patients with high body mass index, should also be considered when initiating insulin therapy.
Verbatim abstract via PubMed 21900381 ↗