Exploring Key Genes to Construct a Diagnosis Model of Dilated Cardiomyopathy

BackgroundDilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and systolic dysfunction. The pathogenesis and etiologies of DCM remain elusive. This study aims to identify the key genes to construct a genetic diagnosis model of DCM. MethodsA total of 257 DCM samples from five independent cohorts were enrolled. The Weighted Gene Co-Expression Network Analysis (WGCNA) was performed to identify the key modules associated with DCM. The latent mechanisms and protein-protein interaction network underlying the key modules were further revealed. Subsequently, we developed and validated a LASSO diagnostic model in five independent cohorts. ResultsTwo key modules were identified using WGCNA. Novel mechanisms related to the extracellular, mitochondrial matrix or IL-17 signaling pathway were pinpointed, which might significantly influence DCM. Besides, 23 key genes were screened out by combining WGCNA and differential expression analysis. Based on the key genes, a genetic diagnosis model was constructed and validated using five cohorts with excellent AUCs (0.975, 0.954, 0.722, 0.850, 0.988). Finally, significant differences in immune infiltration were observed between the two groups divided by the diagnostic model. ConclusionOur study revealed several novel pathways and key genes to provide potential targets and biomarkers for DCM treatment. A key genes' diagnosis model was built to offer a new tool for diagnosing DCM.

Automated summary

This study identified key modules and genes associated with DCM and developed a genetic diagnosis model for DCM, providing new targets and biomarkers for DCM treatment.