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Association between inflammatory bowel disease and pancreatic cancer: results from the two-sample Mendelian randomization study

BackgroundThe nuanced relationship between inflammatory bowel disease (IBD) and pancreatic cancer is noticed in recent years. However, the underlying causal effects of these two diseases are still unclear. MethodsThe two-sample mendelian randomization (MR) was conducted to explore the causal effect...

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Published in:Frontiers in oncology 2023-08, Vol.13, p.1155123-1155123
Main Authors: Min, Yu, Liu, Zheran, Li, Ruidan, Jin, Jing, Wei, Zhigong, Pei, Yiyan, Hu, Xiaolin, Peng, Xingchen
Format: Article
Language:English
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Summary:BackgroundThe nuanced relationship between inflammatory bowel disease (IBD) and pancreatic cancer is noticed in recent years. However, the underlying causal effects of these two diseases are still unclear. MethodsThe two-sample mendelian randomization (MR) was conducted to explore the causal effect of IBD condition on pancreatic cancer. Methods of Wald ratio, inverse variance weighted (IVW), MR-Egger, weighted median, and weighted mode were used to investigate the causal relationship between IBD and pancreatic cancer. Besides, Cochrane's Q test, MR-Egger, and leave-one-out method were further conducted to detect heterogeneity, stability, and pleiotropy of MR results. ResultsIn the MR analysis, we found Crohn's disease had a significant causal effect on pancreatic cancer. Specifically, Crohn's disease would increase 11.1% the risk of pancreatic cancer by the IVW method (p= 0.022), 33.8% by MR Egger (p= 0.015), by 35.3% by the Weighted model (p= 0.005). Regarding ulcerative colitis, there was no statistically significant causal effect observed on pancreatic cancer (p>0.05). Additionally, the pleiotropic test and Leave-one-out analysis both proved the validity and reliability of the present two-sample MR analyses. ConclusionThis study indicates that IBD, particularly Crohn's disease, is causality associated with increased risk of pancreatic cancer. Our results may help public health managers to make better follow-up surveillance of IBD patients.
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1155123