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炎症性肠病增加胰腺炎风险:一项两样本双向孟德尔随机化分析

Inflammatory bowel disease increases the risk of pancreatitis: a two-sample bidirectional Mendelian randomization analysis.

作者信息

Fang Li-Hui, Zhang Jia-Qi, Huang Jin-Ke, Tang Xu-Dong

机构信息

Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.

Institute of Digestive Diseases, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China.

出版信息

BMC Gastroenterol. 2025 Jan 11;25(1):13. doi: 10.1186/s12876-024-03571-7.

Abstract

BACKGROUND

Previous studies have suggested an association between inflammatory bowel disease (IBD), and pancreatitis, including acute pancreatitis (AP) and chronic pancreatitis (CP). We aimed to examine the potential causal relationship between IBD and pancreatitis using the Mendelian randomization (MR) method.

METHODS

We obtained data from genome-wide association studies (GWASs) in European individuals for IBD and its main subtypes, Crohn's disease (CD) and ulcerative colitis (UC) (31,665 IBD cases, 13,768 UC cases, 17,897 CD cases and 33,977 controls). Four independent summary statistics of pancreatitis from the the European Bioinformatics Institute (EMBL-EBI, 10,630 AP cases and 844,679 controls, 1,424 CP cases and 476,104 controls) and FinnGen Consortium (8,446 AP cases, 4,820 CP cases and 437,418 controls) were used for bidirectional MR analyses and sensitivity analysis. Finally, further meta-analysis was conducted on the MR results.

RESULTS

Generally, IBD is associated with an increased risk of pancreatitis (IBD-AP, OR = 1.050, 95% CI 1.020-1.080, P = 7.20 × 10; IBD-CP, OR = 1.050, 95% CI 1.010-1.090, P = 0.019). In addition, UC increased the risk of pancreatitis (UC-AP, OR = 1.050, 95% CI 1.020-1.070, P = 9.10 × 10; UC-CP, OR = 1.090, 95% CI 1.040-1.140, P = 1.44 × 10) and CD increased the risk of acute pancreatitis (OR = 1.040, 95% CI 1.020-1.060, P = 9.61 × 10). However, no causal association was found between CD and the risk of chronic pancreatitis (P > 0.05). The reverse MR results showed that AP may be associated with a reduced risk of IBD and CD (AP-IBD, OR = 0.880, 95% CI 0.810-0.960, P = 0.003; AP-CD, OR = 0.830, 95% CI 0.730-0.940, P = 0.003). However, there is no causal relationship between AP and the risk of UC, and there is no causal relationship between CP and the risk of IBD and its subtypes(P > 0.05).

CONCLUSION

In conclusion, based on MR analysis and meta-analysis, our results showed a positive causal effect of IBD on pancreatitis, and subgroup analyses showed that UC and CD may promote the development of acute pancreatitis, whereas UC may promote the development of chronic pancreatitis. Reverse MR analysis suggests that AP may have a potential protective effect on IBD and CD.

摘要

背景

既往研究提示炎症性肠病(IBD)与胰腺炎之间存在关联,包括急性胰腺炎(AP)和慢性胰腺炎(CP)。我们旨在采用孟德尔随机化(MR)方法研究IBD与胰腺炎之间的潜在因果关系。

方法

我们从欧洲人群的全基因组关联研究(GWAS)中获取了IBD及其主要亚型克罗恩病(CD)和溃疡性结肠炎(UC)的数据(31,665例IBD患者、13,768例UC患者、17,897例CD患者和33,977例对照)。使用来自欧洲生物信息学研究所(EMBL-EBI,10,630例AP患者和844,679例对照、1,424例CP患者和476,104例对照)以及芬兰基因组联盟(8,446例AP患者、4,820例CP患者和437,418例对照)的四项独立的胰腺炎汇总统计数据进行双向MR分析和敏感性分析。最后,对MR结果进行了进一步的荟萃分析。

结果

总体而言,IBD与胰腺炎风险增加相关(IBD-AP,比值比[OR]=1.050,95%置信区间[CI]为1.020-1.080,P=7.20×10;IBD-CP,OR=1.050,95%CI为1.010-1.090,P=0.019)。此外,UC增加了胰腺炎风险(UC-AP,OR=1.050,95%CI为1.020-1.070,P=9.10×10;UC-CP,OR=1.090,95%CI为1.040-1.140,P=1.44×10),CD增加了急性胰腺炎风险(OR=1.040,95%CI为1.020-1.060,P=9.61×10)。然而,未发现CD与慢性胰腺炎风险之间存在因果关联(P>0.05)。反向MR结果显示,AP可能与IBD和CD风险降低相关(AP-IBD,OR=0.880,95%CI为0.81 _ 0.960,P=0.003;AP-CD,OR=0.830,95%CI为0.730-0.940,P=0.003)。然而,AP与UC风险之间不存在因果关系,CP与IBD及其亚型风险之间也不存在因果关系(P>0.05)。

结论

总之,基于MR分析和荟萃分析,我们的结果显示IBD对胰腺炎有正向因果效应,亚组分析表明UC和CD可能促进急性胰腺炎的发生发展,而UC可能促进慢性胰腺炎的发生发展。反向MR分析提示AP可能对IBD和CD具有潜在保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2744/11725204/2afd14e3394a/12876_2024_3571_Fig1_HTML.jpg

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