BMC Infect Dis. 2025 Sep 29;25(1):1199. doi: 10.1186/s12879-025-11575-1.
ABSTRACT
BACKGROUND: Fournier Gangrene (FG) and Generalized Perianal Abscess (GPA) have similar clinical features. But FG has a high mortality and disability rate and needs to be identified and treated as early as possible. This study utilized machine learning methods to integrate clinical and metabolic features to promote early diagnosis of FG.
METHODS: Serological characteristics were screened for patients with FG (n = 20) and GPA (n = 16). The metabolomic changes of FG were described based on untargeted metabolomics. We used machine learning tools to combine demographic data, clinical serology, and metabolomics data to establish disease-specific boundary points.
RESULTS: There were significant differences in the serum metabolic profiles between the FG and GPA groups. 118 different metabolites were detected, mainly fatty acids. Based on machine learning integration of metabolic and clinical features, a differential diagnosis combination of Myo-inositol (MI), Procalcitonin (PCT) and Bistris was established for early identification and diagnosis of FG. The diagnostic performance was evaluated using GBDT, SVM, and LR algorithms, demonstrating robust discriminative ability (AUC: 0.80, 0.82, and 0.95; sensitivity: 0.90, 0.92, and 1.00). In addition, we identified 14 differential metabolic pathways. The activation of Necroptosis may lead to the occurrence of explosive perianal and perineal infections.
CONCLUSION: Our findings provide a biomarker combination for early diagnosis of FG in clinical applications. On the other hand, it provides important insights into the pathological mechanism differences between FG and GPA.
PMID:41023712 | PMC:PMC12482003 | DOI:10.1186/s12879-025-11575-1