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EB病毒与胃炎、胃癌及胃溃疡之间的因果关联:一项双样本孟德尔随机化研究

Causal association between EBV and gastritis, gastric cancer, and gastric ulcer: a two-sample Mendelian randomization study.

作者信息

Qiao Xiaoyuan, Ma Jun, Wang Chunyan, Gou Xing, Huo Lijuan

机构信息

Department of Comprehensive Medicine, Cancer Hospital Affiliated to Shanxi Medical University/Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences, Shanxi Medical University, Taiyuan, 030013, Shanxi, China.

Department of General Surgery, Cancer Hospital Affiliated to Shanxi Medical University/Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences, Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, Shanxi, China.

出版信息

Sci Rep. 2025 Jul 4;15(1):23885. doi: 10.1038/s41598-025-08555-5.

Abstract

Many observational studies have identified a link between Epstein-Barr virus (EBV) and stomach conditions, such as gastric cancer (GC). This study investigated the causal relationship between EBV and GC and conditions that may lead to GC, such as gastritis and gastric ulcer. Data regarding GC were sourced from a FINN cohort; data regarding EBV were obtained from a previous study that relied on the UK Biobank cohort. Inverse-variance weighted (IVW) was used as a primary analysis; Mendelian randomization-Egger (MR-Egger), Weighted median (WM), and weighted model were applied to validate the robustness of the results. MR-Egger regression method was used to explore the presence of horizontal pleiotropy, and the MR pleiotropy residual sum and outlier (MR-PRESSO) method was applied to detect potential outliers. Cochran's Q test was used to test heterogeneity among instrumental variables (IVs). Genetic prediction linked EBV EBNA-1 antibody levels significantly with GC and gastritis, unaffected by horizontal pleiotropy. MR-PRESSO found no outliers for EBNA-1 and GC, but two for gastritis. Heterogeneity was noted in anti-EBV IgG and peptic ulcer, and EBNA-1 and VCA p18 antibodies for gastritis. The present MR analysis provides evidence supporting a causal role for genetically predicted EBNA-1 antibody levels in the etiology of GC. Taking EBV infection into account could help tailor the screening and diagnosis of GC to each patient.

摘要

许多观察性研究已经确定了爱泼斯坦-巴尔病毒(EBV)与胃部疾病之间的联系,如胃癌(GC)。本研究调查了EBV与GC以及可能导致GC的疾病(如胃炎和胃溃疡)之间的因果关系。关于GC的数据来自芬兰队列;关于EBV的数据来自先前一项依赖英国生物银行队列的研究。采用逆方差加权(IVW)作为主要分析方法;使用孟德尔随机化-埃格(MR-Egger)、加权中位数(WM)和加权模型来验证结果的稳健性。采用MR-Egger回归方法探索水平多效性的存在,并应用MR多效性残差和异常值(MR-PRESSO)方法检测潜在异常值。采用 Cochr an Q检验来检验工具变量(IVs)之间的异质性。基因预测表明,EBV EBNA-1抗体水平与GC和胃炎显著相关,不受水平多效性影响。MR-PRESSO未发现EBNA-1与GC之间存在异常值,但发现胃炎存在两个异常值。在抗EBV IgG与消化性溃疡以及EBNA-1与VCA p18抗体在胃炎方面存在异质性。目前的MR分析提供了证据,支持基因预测的EBNA-1抗体水平在GC病因学中的因果作用。考虑EBV感染有助于为每位患者量身定制GC的筛查和诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62c4/12227760/46687e3eaf94/41598_2025_8555_Fig1_HTML.jpg

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