Background
Increasing reports about the association between inflammatory bowel disease (IBD) and pancreatitis have suggested these years. Thus, a two-sample mendelian randomization (MR) study performed to evaluate the causal association between IBD and pancreatitis is necessary.
Methods
We performed univariate two-sample MR and respectively selected single nucleotide polymorphisms (SNPS) associated with IBD, ulcerative colitis (UC), Crohn's disease (CD), acute pancreatitis (AP), and chronic pancreatitis (CP) as instrumental variables (IV). The inverse-variance-weighted method (IVW), MR-Egger, weight mode, simple mode, and weighted median were used in MR analyses, among which IVW is the most important method. Subsequently, the Cochran's Q test, MR-Egger intercept test, leave one-out analyses and funnel plot were used in the sensitivity analysis.
Results
Genetically predicted IBD was positively associated with risk of AP (odds ratio (OR) = 1.062; 95% confidence intervals (CI), 1.01 − 1.11; p = 0.007) and CP (OR = 1.06; 95% CI, 1.00 − 1.13; p = 0.04). Genetically determined UC was suggestively associated with AP (OR = 1.08; 95% CI, 1.03–1.13; p = 0.001), but not CP (OR = 1.00; p = 0.812), and likewise, genetically determined CD was positively correlated with AP (OR = 1.04; 95% CI, 1.00–1.08; p = 0.019), but not CP (OR = 1.04; p = 0.111). It was certified that the results were robust through sensitivity analyses.
Conclusion
Our results identified the causal relationship between IBD and AP/CP, as well as UC/CD and AP, which may influence clinical decisions on the management of IBD patients with pancreatic symptoms.