Key result
Bioinformatics analysis of microarray datasets identified CD14, CD163, and CCR1 as key biomarkers connecting heart and blood mRNA expression in ischemic heart diseases.
Why the study?
Progression of cardiac diseases to heart failure takes years, and using blood samples to monitor cardiac changes before clinical symptoms emerge may improve patient management.
CD14, CD163, and CCR1 were identified as potential blood biomarkers reflecting cardiac changes in ischemic heart disease.
Hypothesis-generating for blood biomarkers in ischemic heart disease; requires prospective validation before clinical consideration.
OBJECTIVE: Cardiac diseases lead to heart failure (HF), but the progression can take several years. Using blood samples to monitor changes in the heart before clinical symptoms begin may help to improve patient management. METHODS: Microarray data GSE42955 and GSE9128 were used as study datasets and GSE16499, GSE57338, and GSE59867 were used as validation groups. The "limma" package from R Language was used to identify differentially expressed genes. Functional enrichment analyses of gene ontology terms and Kyoto Encyclopedia of Genes and Genomes pathways were performed using Database for Annotation, Visualization and Integrated Discovery. We also investigated the correlation between the heart and blood using the mRNA expression level. RESULTS: Three hub genes, CD14, CD163, and CCR1, were identified. Functional enrichment analyses showed their involvement in the immune response and in the inflammatory response, which are the critical biochemical processes in ischemic HF. The mRNA expression level further demonstrated that a special model may exist to help to predict the mRNA level in the heart based on that in blood. CONCLUSIONS: Our study identified three biomarkers that can connect the heart and blood in ischemic heart diseases, which may be a new approach to help better manage ischemic cardiac disease patients.
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Chen et al. (2020) studied Ischemic cardiac diseases. CD14, CD163, and CCR1 biomarkers was evaluated on Differentially expressed genes and functional enrichment. Bioinformatics analysis of microarray datasets identified CD14, CD163, and CCR1 as key biomarkers connecting heart and blood mRNA expression in ischemic heart diseases.
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