Evidence map›Paper›PMID 42540437›Full record

ArticleArchives of medical science : AMS2026

Epstein-Barr virus-related antibody traits and idiopathic pulmonary fibrosis: a bidirectional Mendelian randomization study.

Wentao Wu, Huiying Zhang, Zhe Peng, Shuohao Wang, Xiaozhao Li, Gaojun Xu, Yiqiang Yuan

Abstract read
In one paragraph

Article in Archives of medical science : AMS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Wentao WuHenan Provincial Chest Hospital, Zhengzhou, Henan, China.
Huiying ZhangHenan Provincial Chest Hospital, Zhengzhou, Henan, China.
Zhe PengHenan Provincial Chest Hospital, Zhengzhou, Henan, China.
Shuohao WangChinese University of Hong Kong, Hong Kong, China.
Xiaozhao LiHenan Provincial Chest Hospital, Zhengzhou, Henan, China.
Gaojun XuHenan Provincial Chest Hospital, Zhengzhou, Henan, China.
Yiqiang YuanHenan Provincial Chest Hospital, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Previous studies have suggested an association between herpesvirus infections and idiopathic pulmonary fibrosis (IPF), but the causal relationship remains largely unclear. We used bidirectional Mendelian randomization (MR) to investigate the associations between genetically predicted antibody responses to herpesviruses and IPF risk. Material and methods: The data for different antibodies against herpes simplex virus (HSV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV) were obtained from the IEU GWAS database (https://gwas.mrcieu.ac.uk/datasets/), and the data for IPF were obtained from the FinnGen GWAS database (https://r7.finngen.fi/). We selected eligible single nucleotide polymorphisms (SNPs) from summary-level data of GWAS as instrumental variables. The generalized summary data-based MR (GSMR) method was used as the main analysis method, complemented by inverse-variance weighted (IVW), MR-Egger, and weighted median analyses. Sensitivity analyses were conducted to check the robustness of the MR results, and reverse MR analyses were performed to assess potential reverse causation. Results: Genetically predicted antibody responses to EBV viral capsid antigen (VCA) p18 were associated with IPF risk. However, GSMR and IVW results indicated that anti-EBV IgG levels were significantly negatively associated with IPF. Sensitivity analyses suggested limited influence of horizontal pleiotropy. Conclusions: Genetically predicted EBV-related immune responses show heterogeneous associations with IPF risk. These findings suggest a potential role of EBV-related immune mechanisms in IPF, although causal interpretation should be made cautiously. Further studies are needed to clarify underlying biological mechanisms.

Indexed as

antibody responseherpesvirus-related antibody traitsidiopathic pulmonary fibrosisMendelian randomization

Identifiers

PMID42540437
PMCPMC13426140

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