Integrated machine learning framework identifies EPSTI1 as a key diagnostic biomarker for Sjögren's disease:
Jianbin Li1,2, Renhe Li1,2, Wenwen Wang1,2
1Department of Rheumatism and Immunity, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Objective:
This study aimed to develop a robust transcriptomic diagnostic signature for Sjögren's disease (SjD; formerly Sjögren's syndrome) and elucidate key biomarker functions by integrating machine learning and single-cell analysis.
Methods:
Three SjD peripheral blood datasets (GSE143153, GSE51092, GSE66795; n = 414) were integrated for training, with GSE84844 and GSE40611 for external validation. Candidate biomarkers were identified through differential expression analysis and WGCNA. A total of 113 machine learning algorithm combinations were evaluated. The top biomarker was characterized through SHAP interpretability analysis, immune infiltration profiling, pathway enrichment, genetic colocalization, ceRNA network construction, and RT-qPCR validation. Single-cell RNA sequencing, CellChat, and virtual gene knockout analyses were performed to investigate cell-type expression and regulatory networks.
Results:
Eighty-six core candidate genes were identified. The optimal model (plsRglm + rf) selected 14 diagnostic genes, achieving AUC values of 0.896 (training), 0.871 (GSE84844), and 0.874 (GSE40611). EPSTI1 showed the highest single-gene performance (AUC = 0.844) and significant correlations with IgG (R = 0.64, P = 0.00012) and ANA (R = 0.49, P = 0.0066). SHAP analysis ranked EPSTI1 as the top feature. RT-qPCR in 65 SjD patients and 48 controls confirmed significant EPSTI1 upregulation. Single-cell analysis localized EPSTI1 to monocytes and dendritic cells. CellChat identified enhanced MIF-CD74/CXCR4 signaling, and virtual knockout demonstrated EPSTI1 as a specific downstream effector within the interferon cascade.
Conclusion:
This study established an integrated machine learning framework identifying EPSTI1 as a robust SjD diagnostic biomarker predominantly expressed in myeloid cells. Multi-dimensional validation supports its clinical potential for precision diagnosis of SjD, pending prospective confirmation in larger cohorts. Key Points • A systematic evaluation of 113 machine learning algorithm combinations identified a 14-gene diagnostic signature for Sjögren's disease with robust performance across multiple independent cohorts (AUC > 0.87). • EPSTI1 emerged as the top-ranked diagnostic biomarker through convergent evidence from machine learning feature selection, SHAP interpretability analysis, and RT-qPCR validation in clinical samples. • Single-cell RNA sequencing localized EPSTI1 expression predominantly to monocytes and dendritic cells, linking its diagnostic utility to myeloid-mediated immune dysregulation. • Virtual gene knockout analysis positioned EPSTI1 as a specific downstream effector within the interferon signaling cascade, distinguishing it from broad upstream regulators like STAT1.
