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炎症性肠病与肠易激综合征存在因果关系:一项双向双样本孟德尔随机化研究。

Inflammatory bowel disease is causally related to irritable bowel syndrome: a bidirectional two-sample Mendelian randomization study.

作者信息

Ke Haoran, Li Zitong, Lin Qianyun, Shen Zefeng, Chen Ye, Chen Jinjun

机构信息

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Front Med (Lausanne). 2023 Apr 17;10:1166683. doi: 10.3389/fmed.2023.1166683. eCollection 2023.

Abstract

INTRODUCTION

Inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS) are lifelong digestive diseases that severely impact patients' quality of life. The existence of a causal association between IBS and IBD remains unclear. This study aimed to determine the direction of causality between IBD and IBS by quantifying their genome-wide genetic associations and performing bidirectional two-sample Mendelian randomization (MR) analyses.

METHODS

Genome-wide association studies (GWAS) among a predominantly European patient cohort identified independent genetic variants associated with IBS and IBD. Two separate databases (a large GWAS meta-analysis and the FinnGen cohort) for both IBS and IBD were consulted to retrieve statistics on instrument-outcome associations. MR analyses included inverse-variance-weighted, weighted-median, MR-Egger regression, MR Pleiotropy RESidual Sum and Outlier (MR-PRESSO) methods, and sensitivity analyses were performed. The MR analyses were carried out for each outcome data, followed by a fixed-effect meta-analysis.

RESULTS

Genetically predicted IBD was associated with an increased risk of IBS. Odds ratios (95% confidence intervals) for samples of 211,551 (17,302 individuals with IBD), 192,789 (7,476 Crohn's disease cases), and 201,143 (10,293 ulcerative colitis cases) individuals were 1.20 (1.00, 1.04), 1.02 (1.01, 1.03), and 1.01 (0.99, 1.03), respectively. After outlier correction using MR-PRESSO, the odds ratio for ulcerative colitis was 1.03 (1.02, 1.05) ( = 0.001). However, an association between genetically influenced IBS and IBD was not identified.

DISCUSSION

This study confirms that IBD is causally related to IBS, which may interfere with the diagnosis and treatment of both diseases.

摘要

引言

炎症性肠病(IBD)和肠易激综合征(IBS)是终身性消化系统疾病,严重影响患者的生活质量。IBS与IBD之间是否存在因果关系仍不明确。本研究旨在通过量化全基因组遗传关联并进行双向双样本孟德尔随机化(MR)分析,确定IBD与IBS之间因果关系的方向。

方法

在一个主要为欧洲患者的队列中进行全基因组关联研究(GWAS),以确定与IBS和IBD相关的独立遗传变异。查阅了两个分别针对IBS和IBD的独立数据库(一项大型GWAS荟萃分析和芬兰基因组队列),以获取关于工具-结局关联的统计数据。MR分析包括逆方差加权法、加权中位数法、MR-Egger回归法、MR多效性残差和异常值法(MR-PRESSO),并进行了敏感性分析。对每个结局数据进行MR分析,随后进行固定效应荟萃分析。

结果

遗传预测的IBD与IBS风险增加相关。211,551名个体(17,302名IBD患者)、192,789名个体(7,476例克罗恩病病例)和201,143名个体(10,293例溃疡性结肠炎病例)样本的优势比(95%置信区间)分别为1.20(1.00,1.04)、1.02(1.01,1.03)和1.01(0.99,1.03)。使用MR-PRESSO进行异常值校正后,溃疡性结肠炎的优势比为1.03(1.02,1.05)(P = 0.001)。然而,未发现遗传影响的IBS与IBD之间存在关联。

讨论

本研究证实IBD与IBS存在因果关系,这可能会干扰两种疾病的诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb54/10150057/0037d1816140/fmed-10-1166683-g001.jpg

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