Bile Acid Sequestrant Use and Gastric Cancer: A National Retrospective Cohort Analysis

Author:

Canakis Andrew1,Lee Amy2ORCID,Halvorson Alese E.3,Noto Jennifer M.4,Peek Richard M.45,Wilson Otis67,Hung Adriana78,Roumie Christianne L.789,Greevy Robert38,Shah Shailja C.1011ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, University of Maryland School of Medicine, Baltimore, Maryland, USA;

2. University of California San Diego School of Medicine, San Diego, California, USA;

3. Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA;

4. Division of Gastroenterology, Department of Medicine, Vanderbilt University Medical Center, Nashville Tennessee, USA;

5. Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville Tennessee, USA;

6. Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, USA;

7. VA Tennessee Valley Healthcare System, Clinical Services Research and Development, Nashville, Tennessee, USA;

8. Department of Medicine, Vanderbilt University Medical Center, Nashville Tennessee, USA;

9. VA Geriatrics Research Education and Clinical Center (GRECC), VA Tennessee Valley Health System, Nashville, Tennessee, USA;

10. Gastroenterology Section, VA San Diego Healthcare System, San Diego, California, USA;

11. Division of Gastroenterology, University of California, San Diego, San Diego, California, USA.

Abstract

INTRODUCTION: Bile acids have been implicated in gastric carcinogenesis. We hypothesized that bile acid sequestrant medication (BAM) use is associated with a lower gastric cancer (GC) incidence. METHODS: We assembled a cohort of veterans receiving longitudinal care within the Veterans Health Administration between 2000 and 2020 who completed testing for Helicobacter pylori. The index date was the date of completed H. pylori testing. The primary exposure was the number of filled BAM prescription(s) in the 5 years before the index date. The primary outcome was incident GC, stratified by anatomic subsite. Follow-up began at the index date and ended at the earliest of GC, death, after 2 years of follow-up, or the study end (May 31, 2020). We used Kaplan-Meier curves to visualize differences in GC incidence by exposure group and multivariable Cox proportional hazards models to estimate the association between BAM exposure and anatomic site–specific GC. RESULTS: Among 417,239 individuals (89% male, mean age 54 years, 63% non-Hispanic White), 4,916 (1.2%) filled at least one BAM prescription, 2,623 of whom filled ≥4. Compared with unexposed individuals, those with ≥4 BAM fills before entry had a lower incidence (adjusted hazard ratio 0.71; 95% confidence interval, 0.37–1.36) of GC, but confidence intervals were wide. Results were consistent irrespective of GC anatomic site. DISCUSSION: BAMs may have a protective effect against both cardia and noncardia GC. Further research and external validation are needed to confirm these findings.

Funder

Veterans Affairs Career Development Award

American Gastroenterological Association Research Scholar Award

NIH

VA Clinical Science Research and Development investigator-initiated grant

Center for Diabetes Translation Research

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology

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