Incretin-Based Therapy and Risk of Acute Pancreatitis: A Nationwide Population-Based Case-Control Study
Abstract
OBJECTIVE: To investigate whether the use of incretin-based drugs (GLP-1 receptor agonists and dipeptidyl peptidase 4 [DPP4] inhibitors) is associated with acute pancreatitis. RESEARCH DESIGN AND METHODS: The study was a nationwide population-based case-control study using medical databases in Denmark. Participants were 12,868 patients with a first-time hospitalization for acute pancreatitis between 2005 and 2012 and a population of 128,680 matched control subjects. The main outcome measure was the odds ratio (OR) for acute pancreatitis associated with different antihyperglycemic drugs. We adjusted for history of gallstones, alcoholism, obesity, and other pancreatitis-associated comorbidities and medications. RESULTS: A total of 89 pancreatitis patients (0.69%) and 684 control subjects (0.53%) were ever users of incretins. The crude OR for acute pancreatitis among incretin users was 1.36 (95% CI 1.08–1.69), while it was 1.44 (95% CI 1.34–1.54) among users of other antihyperglycemic drugs. After confounder adjustment, the risk of acute pancreatitis was not increased among incretin users (OR 0.95 [95% CI 0.75–1.21]), including DPP4 inhibitor users (OR 1.04 [95% CI 0.80–1.37]) or GLP-1 receptor agonist users (OR 0.82 [95% CI 0.54–1.23]), or among nonincretin antihyperglycemic drug users (OR 1.05 [95% CI 0.98–1.13]), compared with nonusers of any antihyperglycemic drugs. Findings were similar in current versus ever drug users and in patients with pancreatitis risk factors. The adjusted OR comparing incretin-based therapy with other antihyperglycemic therapy internally while also adjusting for diabetes duration and complications was 0.97 (95% CI 0.76–1.23). CONCLUSIONS: Our findings suggest that the use of incretin-based drugs appears not to be associated with an increased risk of acute pancreatitis.
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The absence of any strong association with pancreatitis for GLP-1RAs has been corroborated by numerous large real-world observational studies of patients with T2D.
“The absence of any strong association with pancreatitis for GLP‐1RAs has been corroborated by numerous large real‐world observational studies of patients with T2D already a decade ago. 99 , 100”
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- Authors
- Thomsen, R. W., Pedersen, L., Møller, N., Kahlert, J., Beck-Nielsen, H., & Sørensen, H. T.
- Affiliations
- Aarhus University Hospital (DK)
- The Danish Centre for Strategic Research in Type 2 Diabetes, Diabetes Research Centre, Department of Endocrinology, Odense University Hospital, Odense, Denmark
- Corresponding author
- Thomsen, Reimar Wernich
- Venue
- Diabetes Care
- Publisher
- American Diabetes Association
- Published
- 2015-01-29
- Volume
- 38
- Issue
- 6
- Pages
- 1089-1098
- ISSN
- 0149-5992 (ISSN-L)
- 1935-5548
- OpenAlex
- W1969969418
- Cited by
- 89
- References
- 32
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 6 · 2023: 5 · 2022: 2 · 2021: 3 · 2020: 7 · 2019: 7 · 2018: 9 · 2017: 6 · 2016: 24 · 2015: 11
- FWCI
- 16.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes Care (publishedVersion)
- PubMed (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (submittedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatitis Pathology and Treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Keywords
- acute pancreatitis, incretin-based therapy, GLP-1 receptor agonists, DPP-4 inhibitors, antidiabetic drugs, drug safety, diabetes mellitus
- MeSH terms
- Acute Disease, Adolescent, Adult, Aged, Denmark, Diabetes Mellitus, Type 2, Epidemiologic Methods, Female, Hospitalization, Humans, Hypoglycemic Agents, Male, Middle Aged, Pancreatitis, Databases, Factual, Glucagon-Like Peptide 1, Incretins, Dipeptidyl-Peptidase IV Inhibitors, Young Adult
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