Abstract

Background: Gastric acid suppressants have a major impact on gut microbiome which in turn, may increase the risk of cholelithiasis, but epidemiological evidence remains unclear. We undertook this research to evaluate the association between regular use of proton pump inhibitors (PPIs) and H2-receptor antagonists (H2RAs) with risk of cholelithiasis. Methods: Prospective cohort study included 477,293 UK residents aged 37–73 years from the UK Biobank. We included the participants reported PPI or H2RA use, and were free of cholelithiasis or cancer. We evaluated hazard ratios (HRs) of regular use of PPIs or H2RAs and risk of cholelithiasis adjusting for demographic factors, lifestyle habits, the presence of comorbidities, use of other medications, and clinical indications. Results: We identified 12,870 cases of cholelithiasis over a median follow-up of 8.1 years. Regular use of PPIs (HR 1.22 95% CI 1.16–1.29) or H2RAs (HR 1.16, 95% CI 1.05–1.28) was associated with an increased risk of cholelithiasis after confounding adjustment. There were no major differences among individual PPIs/H2RAs. The absolute risk of PPI-associated cholelithiasis was increased with the baseline predicted risk evaluated by known environmental and genetic risk factors (Risk differences in the lowest vs. the highest quartile: 1.37 vs. 4.29 per 1,000 person-years). Conclusion: Regular use of PPIs and H2RAs was associated with increased risk of cholelithiasis. Future prospective studies are required to confirm whether the observed associations are casual.

Highlights

  • Cholelithiasis, or gallstone, is one of the most common gastrointestinal diseases

  • We evaluated hazard ratios (HRs) of regular use of pump inhibitors (PPIs) or H2-receptor antagonists (H2RAs) and risk of cholelithiasis adjusting for demographic factors, lifestyle habits, the presence of comorbidities, use of other medications, and clinical indications

  • Regular use of PPIs (HR 1.22 95% confidence intervals (CIs) 1.16–1.29) or H2RAs (HR 1.16, 95% CI 1.05–1.28) was associated with an increased risk of cholelithiasis after confounding adjustment

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Summary

Introduction

Cholelithiasis, or gallstone, is one of the most common gastrointestinal diseases. The prevalence of gallstone disease ranged from 5.9 – 21.9% in Europe (Aerts and Penninckx, 2003). Gastric acid suppressants, including the proton pump inhibitors (PPIs) and H2-receptor antagonists (H2RAs), are commonly used for the treatment of gastroesophageal reflux disease (GERD), peptic ulcer disease, and for the prevention of nonsteroidal anti-inflammatory drug-(NSAID) induced gastrointestinal injury (Freedberg et al, 2017). Long-term use of acid suppressants may promote ductal epithelial proliferation, micropapillary growth of biliary epithelium, focal bile duct stricture formation, and bile duct obstruction (Yang et al, 2020). These morphological changes further facilitate the formation of gallstones. We undertook this research to evaluate the association between regular use of proton pump inhibitors (PPIs) and H2-receptor antagonists (H2RAs) with risk of cholelithiasis

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