Bidirectional analysis shows CRS increases IBD risk and vice versa, suggesting complex interactions.
Prior observational studies suggested an association between chronic rhinosinusitis (CRS) and inflammatory bowel disease (IBD), but causality remains unclear. This study employed a bidirectional 2-sample Mendelian randomization (MR) analysis to investigate potential causal relationships. Genetic variants associated with CRS and IBD (including Crohn’s disease and ulcerative colitis) were sourced from the IEU Open genome-wide association study project. Primary analysis used inverse-variance weighted, supplemented by weighted median and MR-Egger methods. Sensitivity analyses included Cochran’s Q test, MR-Egger intercept, Mendelian Randomization Pleiotropy RESidual Sum and Outlier, and leave-one-out analysis. Inverse-variance weighted revealed CRS increased IBD risk (OR = 1.108, 95% confidence interval = 1.009–1.217, P = .032), while reverse MR indicated IBD increased CRS risk (OR = 1.035, 95% confidence interval = 1.001–1.071, P = .043). No significant causality was found between CRS and IBD subtypes, Crohn’s disease and ulcerative colitis. Sensitivity analyses supported robustness, with no evidence of pleiotropy ( P > .05). This MR study suggests a bidirectional causal relationship between CRS and IBD, though not with subtypes. Further research is needed to elucidate underlying mechanisms.
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Liu et al. (2025) studied this question.
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