多発性硬化症および乾癬における共有診断遺伝子と分子メカニズムのバイオインフォマティクス解析と機械学習による探索
Yuting Kong1, Xinmin Li2, Fangjie Yang1
1Rehabilitation Medicine College, Henan University of Chinese Medicine, Zhengzhou, Henan, 450000, China.
Background:
Multiple sclerosis (MS) and psoriasis are both immune-mediated inflammatory diseases. Previous studies have reported comorbidity between MS and psoriasis, but the underlying mechanisms remain unclear. This study aims to elucidate the shared pathogenesis and core genes underlying MS and psoriasis.
Methods:
Microarray data for MS and psoriasis were downloaded from the GEO database. Differentially expressed genes (DEGs) were analyzed using "limma" package. Functional enrichment analyses were conducted to elucidate biological functions of common DEGs. PPI analysis and machine learning were used to select core genes, and the diagnostic efficacy was evaluated using nomograms. Single-cell analysis and CeRNA network construction were performed. Immune cell infiltration was assessed by single-sample gene set enrichment. Drug prediction, molecular docking and molecular dynamics (MD) simulations identified potential therapeutic drugs.
Results:
89 DEGs identified in MS and psoriasis datasets were enriched in the NOD-like receptor, NF-κB, and JAK-STAT signaling pathways. IL7R and IRF8 were determined as core genes with good diagnostic performance (AUC >0.7). Immune infiltration analysis showed dysregulation of activated CD4 T cells, activated dendritic cells, and gamma delta T cells in both diseases. Single-cell analysis suggested that IL7R and IRF8 were mainly expressed in immune cells. Molecular docking and MD simulations revealed that parthenolide is a potential therapeutic agent.
Conclusion:
This study highlights the critical role of immune dysregulation and chronic inflammation in MS and psoriasis comorbidity. IL7R and IRF8 were identified as core genes and novel intervention targets for both diseases. These findings provide new insights for future research.
