Glucagon-like peptide-1 receptor agonists and risk of acute pancreatitis in patients with type 2 diabetes.
Diabetes Obes Metab · 2017
Last updated 2026-05-28A review of three long-term studies involving 9,347 people taking GLP-1 drugs and 9,353 taking placebos found no increased risk of acute pancreatitis (AP) with GLP-1 drugs compared to placebos (odds ratio 0.745, 95% confidence interval 0.47–1.17). The studies lasted at least 24 months and were designed to carefully track AP cases.
AI summary of the abstract below.
| Journal | Diabetes Obes Metab, 2017 |
|---|---|
| Citations | 119 |
| Relative citation ratio | 4.49 |
| NIH percentile | 91 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes |
Abstract
Glucagon-like peptide-1 receptor agonist (GLP-1RAs) labels warn about acute pancreatitis (AP) and impose upon doctors the obligation to inform patients about symptoms of AP. Here we systematically reviewed the risk of AP in randomized placebo-controlled trials (RCTs) investigating the effect of GLP-1RAs in type 2 diabetes. We performed a systematic review with meta-analysis of long-term (minimum 24 months), placebo-controlled GLP-1RA RCTs in which AP was a predefined adverse event and adjudicated by blinded and independent adjudicating committees. Three high-quality RCTs included a total of 9347 GLP-1RA-treated and 9353 placebo-treated patients with type 2 diabetes. Compared to placebo, treatment with GLP1-RA was not associated with increased risk of AP (Peto odds ratio 0.745 [95% CI, 0.47-1.17]). Trial Sequential Analysis suggested that additional evidence is needed. In conclusion, this review found no evidence that treatment with GLP-1RA increases the risk of AP in patients with type 2 diabetes.
Verbatim abstract via PubMed 28105738 ↗