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pmid:40750912
Identifying pyroptosis-related genes as novel therapeutic targets in diabetic foot ulceration.
Kang Liu · Lei Lei · Xin-Lei Yang · Xin-He Zhang
Diabetology & metabolic syndrome · 2025 doi:10.1186/s13098-025-01880-9
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Experiment
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Data
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Analysis
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Complete file
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During the treatment of DFU, the locally intense inflammatory response induced by pyroptosis may adversely affect wound healing, making this phenomenon a focus of research. This study employed bioinformatics methods to systematically analyze the role of pyroptosis-related genes (PRGs) in the healing process of diabetic foot ulcers. Based on public datasets GSE147890 and GSE80178, we performed differential expression analysis, random forest, and LASSO regression to screen for key genes, and constructed and evaluated a multivariate logistic regression diagnostic model. We analyzed the GEO datasets GSE147890 and GSE80178, identifying 1336 and 2727 differentially expressed genes (DEGs), respectively. The intersection analysis with PRGs revealed 9 pyroptosis-related differentially expressed genes (PRDEGs). Functional enrichment analysis associated these genes with pathways such as I-kappaB kinase/nuclear factor-kappaB (IKK/NF-κB) signaling and mitophagy. 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