Causal Inference and Shared Molecular Pathways in Crohn’s Disease, Celiac Disease, and Ankylosing Spondylitis: Integrative Mendelian Randomization and Transcriptomic Analysis

This study explored the causal and molecular overlap among Crohn's disease (CD), celiac disease (CeD), and ankylosing spondylitis (AS). Bidirectional Mendelian randomization revealed significant causal associations between each disease pair. Transcriptomic analyses identified three consistently upregulated hub genes-P2RY8, ITGAL, and GPR65-across all conditions, which were validated in independent datasets and inflammatory cell models. Functional enrichment suggested these genes are involved in immune signaling and mucosal inflammation. Regulatory network and molecular docking analyses further highlighted Trichostatin A as a potential therapeutic agent. These findings reveal shared genetic and immune-related mechanisms, offering novel targets for cross-disease treatment strategies.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-07-04
DOI
https://doi.org/10.3390/ijms26136451
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

Causal Inference and Shared Molecular Pathways in Crohn’s Disease, Celiac Disease, and Ankylosing Spondylitis: Integrative Mendelian Randomization and Transcriptomic Analysis

Zheng‐Qiang Wei, Mingzhu Zhang, Ya Li, Xin Yang et al.
1 links
International Journal of Molecular Sciences
Inflammatory Bowel Disease
article

Causal Inference and Shared Molecular Pathways in Crohn’s Disease, Celiac Disease, and Ankylosing Spondylitis: Integrative Mendelian Randomization and Transcriptomic Analysis

Zheng‐Qiang Wei, Mingzhu Zhang, Ya Li, Xin Yang, Shihao Xu
article en

Abstract

This study explored the causal and molecular overlap among Crohn's disease (CD), celiac disease (CeD), and ankylosing spondylitis (AS). Bidirectional Mendelian randomization revealed significant causal associations between each disease pair. Transcriptomic analyses identified three consistently upregulated hub genes-P2RY8, ITGAL, and GPR65-across all conditions, which were validated in independent datasets and inflammatory cell models. Functional enrichment suggested these genes are involved in immune signaling and mucosal inflammation. Regulatory network and molecular docking analyses further highlighted Trichostatin A as a potential therapeutic agent. These findings reveal shared genetic and immune-related mechanisms, offering novel targets for cross-disease treatment strategies.

International Journal of Molecular SciencesVol. 26(13)
The Affiliated Yongchuan Hospital of Chongqing Medical University (CN)
Good health and well-being
Openalex Percentile: Top 81%
Inflammatory Bowel Disease
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