GLPwatch

The Clinical Efficacy and Safety of Glucagon-Like Peptide-1 (GLP-1) Agonists in Adults with Type 2 Diabetes Mellitus.

Clin Med Insights Endocrinol Diabetes · 2011

Last updated 2026-05-28

A review of studies found that two GLP-1 drugs, exenatide and liraglutide, improved blood sugar control in adults with type 2 diabetes, led to weight loss, and supported better function of insulin-producing cells. These benefits were seen both when used alone and with other diabetes medications. The most common side effects were temporary stomach issues like nausea.

AI summary of the abstract below.

JournalClin Med Insights Endocrinol Diabetes, 2011
Citations2
Relative citation ratio0.06
NIH percentile5
Molecules
Conditions studied Type 2 Diabetes

Abstract

OBJECTIVE: To review the efficacy and safety of glucagon-like peptide-1 (GLP-1) agonists to determine their role in type 2 diabetes mellitus (T2DM). DATA SOURCES: A Medline search was conducted using the keywords exenatide, liraglutide, glucagon-like peptide-1, type 2 diabetes mellitus, hyperglycemia, pharmacokinetics, pharmacology and safety. STUDY SELECTION: All identified articles written in English were evaluated with priority given to controlled, randomized trials including human data. References of identified published trials were reviewed for additional trials to be included in the review. DATA SYNTHESIS: Exenatide and liraglutide are GLP-1 agonists approved for the treatment of T2DM. Several randomized, active and placebo controlled trials examining the efficacy and safety of exenatide and liraglutide both as monotherapy and in combination therapy have been conducted. Both agents have demonstrated improved glycemic control in addition to weight loss and increased beta-cell function. The most common adverse effects are gastrointestinal in nature and appear to be transient. CONCLUSION: It appears exenatide and liraglutide are safe and effective in the treatment of T2DM and may exhibit effects that make them preferred over other anti-diabetic medications.

Verbatim abstract via PubMed 22879790 ↗