Li Ya, Xu Shihao, Zhang Mingzhu, Yang Xin, Wei Zhengqiang
First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China.
Int J Mol Sci. 2025 Jul 4;26(13):6451. doi: 10.3390/ijms26136451.
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.
本研究探讨了克罗恩病(CD)、乳糜泻(CeD)和强直性脊柱炎(AS)之间的因果关系和分子重叠。双向孟德尔随机化揭示了每对疾病之间存在显著的因果关联。转录组分析确定了在所有疾病状态下均持续上调的三个核心基因——P2RY8、ITGAL和GPR65,这些基因在独立数据集和炎症细胞模型中得到了验证。功能富集分析表明这些基因参与免疫信号传导和黏膜炎症。调控网络和分子对接分析进一步强调曲古抑菌素A是一种潜在的治疗药物。这些发现揭示了共同的遗传和免疫相关机制,为跨疾病治疗策略提供了新的靶点。