Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease with limited treatment options and frequent drug resistance. Novel therapeutic targets are urgently needed. We performed a druggable genome‐wide Mendelian randomization (MR) analysis using blood cis‐expression quantitative trait locus (eQTL) and HS genome‐wide association study (GWAS) data. Colocalization, transcriptomic validation, single‐cell RNA sequencing, and cell–cell communication analyses were integrated to explore gene function and cell‐type specificity. We identified eight genes that showed significant associations with HS through MR analysis. Colocalization analysis further prioritized PSMA4 and MAST3 as the most promising druggable targets for HS. Specifically, PSMA4 (single nucleotide polymorphisms SNPs = 10; inverse‐variance weighted IVW OR = 1.912, 95% CI: 1.492–2.450, p < 0.001; PP.H4 = 0.975) and MAST3 (SNPs = 15; IVW OR = 0.557, 95% CI: 0.453–0.686, p < 0.001; PP.H4 = 0.832) exhibited strong statistical associations. Transcriptomic validation revealed that PSMA4 was upregulated and MAST3 was downregulated in HS lesions. Further single‐cell analysis revealed that PSMA4 was predominantly enriched in CD4 + T cells and involved in pro‐inflammatory signaling, particularly the tumor necrosis factor (TNF) pathway. PSMA4 and MAST3 are potential therapeutic targets for HS. PSMA4 may promote inflammation via CD4 + T cell‐mediated signaling, offering a novel avenue for treatment development.
Guo et al. (Thu,) studied this question.