• Identified 37 druggable genes associated with osteoporosis, with troponin C2 and CXCR6 showing protective effects and shared causal variants.
• CXCR6 expression was significantly reduced in osteoporosis, and single-cell analysis revealed its predominant expression on T cells with enhanced cell communication.
• Drug enrichment and molecular docking identified NSC95397 as a potential CXCR6-targeting compound with good binding activity.
• The study provides novel insights into osteoporosis pathogenesis and potential therapeutic targets, supporting translational applications.
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