Key result
Hub genes IL-6 and RHOA show high diagnostic accuracy for ischemic cardiomyopathy, reaching AUC ~0.99.
Why the study?
Myocardial ischemia and hypoxia cause myocardial cell necrosis and scar formation, but potential biomarkers for early diagnosis and treatment of ischemic cardiomyopathy remain to be identified.
Observational (n=17)
Effect estimate: AUC 0.956 for IL-6 and 0.995 for RHOA
p-value: p=<0.05
May support biomarker discovery in ischemic cardiomyopathy; leaves open prospective validation before clinical adoption.
Background: Myocardial ischemia and hypoxia may result in myocardial cell necrosis, scar formation, and hyperplasia. We aim to explore the differentially expressed genes (DEGs) in ischemic cardiomyopathy (ICM), construct and identify a clinical prognosis model using bioinformatics methods, so as to screen potential biomarkers of ICM to provide a basis for the early diagnosis and treatment of ICM. Methods: Based on the National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (GEO) database, R language was used to screen DEGs in healthy myocardial (n=5) and ICM myocardial tissues (n=12). DEGs were analyzed by Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and protein-protein interaction (PPI). Receiver operating characteristic (ROC) curves were drawn to verify the target genes. Results: A total of 259 genes with significantly changed fold change (FC) values were obtained through conditional screening, including up-regulated genes and down-regulated genes. The first two hub genes [interleukin-6 (IL-6) and Ras homologous gene family member A (RHOA)] with the largest degree value among the above up-regulated and down-regulated genes were selected and their expression values were combined in the gene chip to draw the ROC curve based on the pROC package of R language. The area under the ROC curve (AUC) values of IL-6 and RHOA were 0.956 and 0.995, respectively. The expression levels of Sqstm1, Nos2, IL-6, RHOA, and Zfp36 genes in the ICM group are lower than those in the blank control group and the difference was statistically significant (P<0.05). RHOA and Stat3 were identified as the key genes controlling the occurrence and development of ICM. Conclusions: ICM is closely related to the changes of extracellular matrix (ECM) and oxidoreductase activity. The IL-6 and RHOA are expected to become potential targets for ICM treatment.
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Wang et al. (2024) conducted an observational in Ischemic cardiomyopathy (n=17). Ischemic cardiomyopathy vs. Healthy myocardial tissues was evaluated on Diagnostic performance (AUC) of hub genes IL-6 and RHOA (AUC 0.956 for IL-6 and 0.995 for RHOA, p=<0.05). The hub genes IL-6 and RHOA demonstrated high diagnostic accuracy for ischemic cardiomyopathy, with AUC values of 0.956 and 0.995, respectively.
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