학술논문

Thiazide Diuretics and Risk of Colorectal Cancer: A Population-Based Cohort Study.
Document Type
Article
Source
American Journal of Epidemiology. Jan2024, Vol. 193 Issue 1, p47-57. 11p.
Subject
*HYPERTENSION
*ANTIHYPERTENSIVE agents
*DIURETICS
*CONFIDENCE intervals
*INFLAMMATORY bowel diseases
*CALCIUM antagonists
*COLORECTAL cancer
*RISK assessment
*COMPARATIVE studies
*DESCRIPTIVE statistics
*POLYPS
*POPULATION-based case control
*RESEARCH funding
*ODDS ratio
*LONGITUDINAL method
*PROPORTIONAL hazards models
*DISEASE risk factors
Language
ISSN
0002-9262
Abstract
Evidence from clinical trials and observational studies on the association between thiazide diuretics and colorectal cancer risk is conflicting. We aimed to determine whether thiazide diuretics are associated with an increased colorectal cancer risk compared with dihydropyridine calcium channel blockers (dCCBs). A population-based, new-user cohort was assembled using the UK Clinical Practice Research Datalink. Between 1990–2018, we compared thiazide diuretic initiators with dCCB initiators and estimated hazard ratios (HR) with 95% confidence intervals (CIs) of colorectal cancer using Cox proportional hazard models. Models were weighted using standardized morbidity ratio weights generated from calendar time-specific propensity scores. The cohort included 377,760 thiazide diuretic initiators and 364,300 dCCB initiators, generating 3,619,883 person-years of follow-up. Compared with dCCBs, thiazide diuretics were not associated with colorectal cancer (weighted HR = 0.97, 95% CI: 0.90, 1.04). Secondary analyses yielded similar results, although an increased risk was observed among patients with inflammatory bowel disease (weighted HR = 2.45, 95% CI: 1.13, 5.35) and potentially polyps (weighted HR = 1.46, 95% CI: 0.93, 2.30). Compared with dCCBs, thiazide diuretics were not associated with an overall increased colorectal cancer risk. While these findings provide some reassurance, research is needed to corroborate the elevated risks observed among patients with inflammatory bowel disease and history of polyps. [ABSTRACT FROM AUTHOR]