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Association between incretin-based drugs and risk of cholangiocarcinoma among patients with type 2 diabetes: A large population-based matched cohort study.

Title: Association between incretin-based drugs and risk of cholangiocarcinoma among patients with type 2 diabetes: A large population-based matched cohort study.
Authors: Krishnan A; Department of Supportive Oncology, Atrium Health Levine Cancer, Charlotte, NC, USA.; Department of Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.; Schneider CV; Department of Internal Medicine III, RWTH Aachen University, Aachen, Germany.; Arkenau HT; Sarah Cannon Research Institute, Cancer Institute, University College London, London, UK.; Mauro EM; Barcelona Clinic Liver Cancer Group, Liver Unit, Hospital Clinic Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Madrid, Spain.; Forner A; Barcelona Clinic Liver Cancer Group, Liver Unit, Hospital Clinic Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Madrid, Spain.; Scott Butsch W; Bariatric and Metabolic Institute, Cleveland Clinic, Cleveland, OH, USA.; Walsh D; Department of Supportive Oncology, Atrium Health Levine Cancer, Charlotte, NC, USA.; Alqahtani SA; Organ Transplant Center of Excellence, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.; Division of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, NY, USA.
Source: Journal of clinical & translational endocrinology [J Clin Transl Endocrinol] 2024 Sep 18; Vol. 38, pp. 100370. Date of Electronic Publication: 2024 Sep 18 (Print Publication: 2024).
Publication Type: Journal Article
Language: English
Journal Info: Publisher: Elsevier Inc Country of Publication: Netherlands NLM ID: 101629335 Publication Model: eCollection Cited Medium: Internet ISSN: 2214-6237 (Electronic) Linking ISSN: 22146237 NLM ISO Abbreviation: J Clin Transl Endocrinol Subsets: PubMed not MEDLINE
Imprint Name(s): Original Publication: [Amsterdam] : Elsevier Inc.
Abstract: Aim: To examine the association between the use of incretin-based drugs [glucagon-like peptide-1 receptor agonists (GLP-1RAs), dipeptidyl peptidase-4 inhibitors (DPP-4Is)] and the risk of cholangiocarcinoma (CCA) in the United States.; Methods: This large population-based, retrospective cohort study using the TriNetX datasets included adult patients with type 2 diabetes mellitus (T2DM) who were new users of GLP-1RAs, DPP-4Is, or other second- or third-line antidiabetic drugs between 2010 and 2021. The primary outcome was the incidence of CCA.; Results: A total of 3,816,071 patients were included (mean age, 61.4 years, female, 49.3 %). A 51 % and 23 % risk reduction in CCA after 1 year of exposure to GLP-1RAs (hazard ratio 0.49; 95 % CI 0.40-0.60) and DPP4Is (0.77, 95 % CI 0.67-0.90), respectively compared to new second-or third-line users. Results were consistent at 3, 5, and 7 years of follow-up (0.66, 0.71, and 0.72 for GLP-1RAs and 0.84, 0.87, and 0.85 for DPP-4Is, respectively). Compared to new metformin users, GLP-1RA users were associated with a 42 % lower risk of developing CCA, whereas DPP-4I group was not associated with an increased risk.; Conclusions: GLP-1RAs and DPP-4Is were not associated with a significantly increased risk of CCA. GLP-1RAs even showed a reduced risk of CCA development. They can be considered as safe and effective treatment options for patients with T2DM at risk of CCA.; (© 2024 The Author(s).)
Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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Contributed Indexing: Keywords: Cholangiocarcinoma; Dipeptidyl peptidase 4 inhibitors; Glucagon-like peptide-1 receptor agonists; Incretin; Type 2 diabetes mellitus
Entry Date(s): Date Created: 20241010 Latest Revision: 20241011
Update Code: 20260130
PubMed Central ID: PMC11460491
DOI: 10.1016/j.jcte.2024.100370
PMID: 39386155
Database: MEDLINE

Journal Article