Identification and validation of novel candidate genes with diagnostic value for sepsis via weighted gene co-expression network analysis - Report - MDSpire
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Identification and validation of novel candidate genes with diagnostic value for sepsis via weighted gene co-expression network analysis
Clinical Report: Discovery and validation of new candidate genes for sepsis
Overview
This study identified five candidate genes associated with sepsis and evaluated their diagnostic potential using bioinformatics tools. A logistic regression model demonstrated discriminative ability for diagnosing sepsis in both training and validation cohorts.
Background
Sepsis is a significant global health issue characterized by high morbidity and mortality rates. Accurate and timely diagnosis remains challenging due to the complex nature of its pathogenesis and the lack of specific therapeutic drugs.
Data Highlights
WGCNA identified 1,463 sepsis-associated genes, with five hub genes (CDK1, CCNB1, CCNA2, AURKB, BUB1) showing high expression in sepsis. The logistic regression model based on these genes achieved AUC values of 0.747 in the training set and 0.799 in the validation cohort.
Key Findings
Five hub genes (CDK1, CCNB1, CCNA2, AURKB, BUB1) were identified as sepsis-associated.
Higher expression of AURKB or BUB1 was observed.
The logistic regression model demonstrated AUC values of 0.747 and 0.799 for distinguishing sepsis from healthy controls.
The model also differentiated septic shock from cardiogenic shock (AUC = 0.743) and non-septic shock (AUC = 0.766).
Significant correlations were found between gene expression and immune cell infiltration in sepsis.
Clinical Implications
Further validation in prospective cohorts is necessary to establish the clinical utility of the identified genes.
Conclusion
The study identifies specific genes as diagnostic markers for sepsis, requiring further validation.