Glucagonlike peptide 1-based therapies and risk of hospitalization for acute pancreatitis in type 2 diabetes mellitus: a population-based matched case-control study
- PMID: 23440284
- DOI: 10.1001/jamainternmed.2013.2720
Glucagonlike peptide 1-based therapies and risk of hospitalization for acute pancreatitis in type 2 diabetes mellitus: a population-based matched case-control study
Abstract
Importance: Acute pancreatitis has significant morbidity and mortality. Previous studies have raised the possibility that glucagonlike peptide 1 (GLP-1)-based therapies, including a GLP-1 mimetic (exenatide) and a dipeptidyl peptidase 4 inhibitor (sitagliptin phosphate), may increase the risk of acute pancreatitis.
Objective: To test whether GLP-1-based therapies such as exenatide and sitagliptin are associated with an increased risk of acute pancreatitis. We used conditional logistic regression to analyze the data.
Design: Population-based case-control study.
Setting: A large administrative database in the United States from February 1, 2005, through December 31, 2008.
Participants: Adults with type 2 diabetes mellitus aged 18 to 64 years. We identified 1269 hospitalized cases with acute pancreatitis using a validated algorithm and 1269 control subjects matched for age category, sex, enrollment pattern, and diabetes complications.
Main outcome measure: Hospitalization for acute pancreatitis.
Results: The mean age of included individuals was 52 years, and 57.45% were male. Cases were significantly more likely than controls to have hypertriglyceridemia (12.92% vs 8.35%), alcohol use (3.23% vs 0.24%), gallstones (9.06% vs 1.34), tobacco abuse (16.39% vs 5.52%), obesity (19.62% vs 9.77%), biliary and pancreatic cancer (2.84% vs 0%), cystic fibrosis (0.79% vs 0%), and any neoplasm (29.94% vs 18.05%). After adjusting for available confounders and metformin hydrochloride use, current use of GLP-1-based therapies within 30 days (adjusted odds ratio, 2.24 [95% CI, 1.36-3.68]) and recent use past 30 days and less than 2 years (2.01 [1.37-3.18]) were associated with significantly increased odds of acute pancreatitis relative to the odds in nonusers.
Conclusions and relevance: In this administrative database study of US adults with type 2 diabetes mellitus, treatment with the GLP-1-based therapies sitagliptin and exenatide was associated with increased odds of hospitalization for acute pancreatitis.
Comment in
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Glucagonlike Peptide 1-based drugs and pancreatitis: clarity at last, but what about pancreatic cancer?JAMA Intern Med. 2013 Apr 8;173(7):539-41. doi: 10.1001/jamainternmed.2013.3374. JAMA Intern Med. 2013. PMID: 23463371 No abstract available.
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Glucagon-like peptide 1-based drugs and pancreatic safety.JAMA Intern Med. 2013 Oct 28;173(19):1842-3. doi: 10.1001/jamainternmed.2013.8138. JAMA Intern Med. 2013. PMID: 24165844 No abstract available.
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Glucagon-like peptide 1-based drugs and pancreatic safety.JAMA Intern Med. 2013 Oct 28;173(19):1843. doi: 10.1001/jamainternmed.2013.8150. JAMA Intern Med. 2013. PMID: 24165845 No abstract available.
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Glucagon-like peptide 1-based drugs and pancreatic safety--reply.JAMA Intern Med. 2013 Oct 28;173(19):1843-4. doi: 10.1001/jamainternmed.2013.8128. JAMA Intern Med. 2013. PMID: 24165846 No abstract available.
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