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Published on: April 16, 2019
Cohort Study: Risk of Gallstones and Biliary Complications With Glucagon-Like Peptide-1 Receptor Agonists in Type 2
Mohamed H Eldesouki1, Omar Alkasabrah2, Mohammed Kloub1
1Department of Internal Medicine, New York Medical College at Saint Michael's Medical Center, Newark, New Jersey, USA.
Background:
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are widely prescribed for type 2 diabetes mellitus (T2DM) because of their benefits in glycemic control, weight reduction, and cardiovascular outcomes. This study evaluated the risk of gallbladder disease among diabetic patients treated with GLP-1 RAs.
Methods:
A retrospective cohort analysis was performed using the TriNetX research network. Adults ≥ 18 years with T2DM who received GLP-1 RAs were identified and compared with matched controls. Propensity score matching (1:1) was used to balance baseline characteristics. Outcomes included cholelithiasis/choledocholithiasis, cholecystitis, pancreatitis, endoscopic retrograde cholangiopancreatography (ERCP), and cholecystectomy. Subgroup analyses were performed according to GLP-1 RA agents.
Results:
A total of 156,376 patients were included; 43,077 patients were in the GLP-1 RA cohort and 113,299 patients were in the control group. After matching, 39,140 patients remained in each group. At two years, patients with GLP-1 RA use had higher rates of cholelithiasis/choledocholithiasis (aOR 1.44, 95% CI 1.24-1.65), whereas rates of cholecystectomy were non-significant. By three years, GLP-1 RA use remained associated with higher rates of cholelithiasis/choledocholithiasis (aOR 1.43, 95% CI 1.24-1.63), cholecystitis (aOR 1.45, 95% CI 1.14-1.83), and cholecystectomy (aOR 1.54, 95% CI 1.17-2.02). There were no significant differences in the rates of pancreatitis or ERCP. Semaglutide and dulaglutide demonstrated higher cholelithiasis, whereas liraglutide and exenatide were not associated with a significant increase.
Conclusion:
GLP-1 RAs use in patients with T2DM was associated with modestly higher rates of cholelithiasis/choledocholithiasis, cholecystitis, and cholecystectomy, whereas there were no significant differences in rates of pancreatitis or ERCP.
Insights
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may increase the risk of gallbladder disease in type 2 diabetes patients. This includes higher rates of gallstones, cholecystitis, and cholecystectomy, but not pancreatitis.
Area of Science:
- Endocrinology
- Gastroenterology
- Pharmacology
Background:
- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are crucial for managing type 2 diabetes mellitus (T2DM).
- These agents offer benefits in glycemic control, weight reduction, and cardiovascular health.
- The potential association between GLP-1 RAs and gallbladder disease requires thorough investigation.
Purpose of the Study:
- To evaluate the risk of gallbladder disease in patients with T2DM treated with GLP-1 RAs.
- To compare the incidence of various gallbladder-related outcomes between GLP-1 RA users and matched controls.
- To explore potential differences in risk among specific GLP-1 RA agents.
Main Methods:
- A retrospective cohort analysis was conducted using the TriNetX research network.
- Adult patients with T2DM treated with GLP-1 RAs were compared to propensity score-matched controls.
- Outcomes assessed included cholelithiasis, choledocholithiasis, cholecystitis, pancreatitis, ERCP, and cholecystectomy.
Main Results:
- GLP-1 RA use was associated with increased rates of cholelithiasis/choledocholithiasis at two and three years.
- By three years, GLP-1 RA use also showed higher rates of cholecystitis and cholecystectomy.
- No significant differences in pancreatitis or ERCP rates were observed between groups. Semaglutide and dulaglutide showed higher cholelithiasis risk.
Conclusions:
- GLP-1 RA use in T2DM patients is linked to a modest increase in gallbladder disease.
- The study highlights increased risks for gallstones, cholecystitis, and cholecystectomy.
- Pancreatitis and ERCP rates were not significantly affected by GLP-1 RA treatment.
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