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Published on: January 28, 2020
Bioinformatics Analysis to Find Novel Biomarkers for Coronary Heart Disease
Akram Gholipour1, Farshad Shakerian2,3, Ali Zahedmehr3
1Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Insights
Researchers identified potential biomarkers for coronary heart disease (CHD) by analyzing blood exosome RNA expression. ACSBG1 and DEFA4 show promise for early CHD detection, pending further validation.
Area of Science:
- Biochemistry
- Genomics
- Molecular Biology
Background:
- Coronary heart disease (CHD) is a leading global cause of mortality.
- CHD involves the narrowing or blockage of coronary arteries supplying the heart.
- Identifying reliable biomarkers is crucial for early diagnosis and management of CHD.
Purpose of the Study:
- To identify novel RNA biomarkers for coronary artery disease (CAD).
- To compare the expression profiles of blood exosomes from normal and CHD individuals.
- To discover potential molecular indicators for early CHD detection.
Main Methods:
- Downloaded and analyzed RNA sequencing data from 6 CHD and 6 normal blood exosome samples.
- Identified differentially expressed RNAs using adjusted P-value < 0.01 and log2FoldChange ≥ 1.
- Performed Gene Ontology (GO) and pathway analysis using the PANTHER database.
Main Results:
- Identified 119 differentially expressed genes between CHD and normal samples.
- Candidate biomarkers include the downregulated gene ACSBG1 and the upregulated gene DEFA4.
- Enriched pathways involve metabolic processes, inflammation, immune response, and stimulus response, all linked to cardiovascular disease.
Conclusions:
- Proposed ACSBG1 and DEFA4 as potential specific biomarkers for CHD.
- Highlighted the role of identified pathways in cardiovascular disease pathogenesis.
- Emphasized the need for experimental validation to confirm biomarker suitability for early CHD detection.
Background:
Coronary heart disease (CHD), a major cause of death worldwide, is defined as a narrowing or blockage of the coronary arteries that supply oxygen and blood to the heart. We aimed to find potential biomarkers for coronary artery disease, by comparing the expression profile of blood exosomes of both normal and CHD samples.
Methods:
Datasets of 6 CHD and 6 normal samples of blood exosomes were downloaded, and differentially expressed RNAs, with adjusted P<0.01 and log2FoldChange≥1 were achieved. Moreover, gene ontology (GO) and pathway analysis were accomplished by PANTHER database for datasets.
Results:
Our data analysis found 119 differentially expressed genes between two datasets. By comparing transcriptome profiles, we candidate the highest downregulated gene, ACSBG1, and the highest upregulated one, DEFA4, as specific biomarkers for CHD. Furthermore, GO and pathway analysis depicted that aforementioned differentially expressed genes are mostly involved in different molecular metabolic process, inflammation, immune system process and response to stimulus pathways which all cause cardiovascular diseases.
Conclusion:
We have provided new potential biomarkers for CHD, though experimental validation is still needed to confirm the suitability of the candidate genes for early detection of CHD.
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