Proton pump inhibitors and the risk of inflammatory bowel disease: population-based cohort study.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 36717221.
- Also identified by DOI 10.1136/gutjnl-2022-328866.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
To determine whether the use of proton pump inhibitors (PPIs) compared with the use of histamine-2 receptor antagonists (H2RAs) is associated with an increased risk of inflammatory bowel disease (IBD). Population-based cohort study designed to address the impact of protopathic bias. General practices contributing data to the UK Clinical Practice Research Datalink GOLD. 1 498 416 initiators of PPIs and 322 474 initiators of H2RAs from 1 January 1990 to 31 December 2018, with follow-up until 31 December 2019. Patients were analysed according to the timing of the IBD diagnosis after treatment initiation (early vs late). Standardised morbidity ratio weighted Cox proportional hazards models were used to estimate marginal HRs and 95% CIs. In the early-event analysis, IBD diagnoses were assessed within the first 2 years of treatment initiation, an analysis subject to potential protopathic bias. In the late-event analysis, all exposures were lagged by 2 years to account for latency and minimise protopathic bias. In the early-event analysis, the use of PPIs was associated with an increased risk of IBD within the first 2 years of treatment initiation, compared with H2RAs (HR 1.39, 95% CI 1.14 to 1.69). In contrast, the use of PPIs was not associated with an increased risk of IBD in the late-event analysis (HR 1.05, 95% CI 0.90 to 1.22). The results remained consistent in several sensitivity analyses. Compared with H2RAs, PPIs were not associated with an increased risk of IBD, after accounting for protopathic bias.
Medical subject headings
- Proton Pump Inhibitors
- Inflammatory Bowel Diseases