GLP-1 Agonists in Type 1 Diabetes Mellitus.
Ann Pharmacother · 2016
Last updated 2026-05-28In 9 clinical trials, GLP-1 drugs in people with type 1 diabetes lowered blood sugar slightly—by up to 0.6%—but the average drop was only 0.1% to 0.2% compared to control groups. Participants lost up to 6.4 kg over 24 weeks, though many reported nausea. The drugs did not increase low blood sugar compared to insulin alone.
AI summary of the abstract below.
| Journal | Ann Pharmacother, 2016 |
|---|---|
| Citations | 36 |
| Relative citation ratio | 1.32 |
| NIH percentile | 60 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes |
Abstract
OBJECTIVE: To review the use of GLP-1 agonists in patients with type 1 diabetes mellitus (T1DM).
DATA SOURCES: A search using the MEDLINE database, EMBASE, and Cochrane Database was performed through March 2016 using the search terms glucagon-like peptide 1 (GLP-1) agonists, incretin, liraglutide, exenatide, albiglutide, dulaglutide, type 1 diabetes mellitus
STUDY SELECTION AND DATA EXTRACTION: All English-language trials that examined glycemic end points using GLP-1 agonists in humans with T1DM were included.
DATA SYNTHESIS: A total of 9 clinical trials examining the use of GLP-1 agonists in T1DM were identified. On average, hemoglobin A1C (A1C) was lower than baseline, with a maximal lowering of 0.6%. This effect was not significant when tested against a control group, with a relative decrease in A1C of 0.1% to 0.2%. In all trials examined, reported hypoglycemia was low, demonstrating no difference when compared with insulin monotherapy. Weight loss was seen in all trials, with a maximum weight loss of 6.4 kg over 24 weeks. Gastrointestinal adverse effects are potentially limiting, with a significant number of patients in trials reporting nausea.
CONCLUSION: The use of GLP-1 agonists should be considered in T1DM patients who are overweight or obese and not at glycemic goals despite aggressive insulin therapy; however, tolerability of these agents is a potential concern. Liraglutide has the strongest evidence for use and would be the agent of choice for use in overweight or obese adult patients with uncontrolled T1DM.
Verbatim abstract via PubMed 27252246 ↗