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Identification of the Difference in the Pathogenesis in Heart Failure Arising from Different Etiologies Using a Microarray Dataset

Overview
Publisher Elsevier
Specialty General Medicine
Date 2017 Nov 22
PMID 29160422
Citations 7
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Abstract

Objectives: Clinically, patients with chronic heart failure arising from different etiologies receive the same treatment. However, the prognoses of these patients differ. The purpose of this study was to elucidate whether the pathogenesis of heart failure arising from different etiologies differs.

Methods: Heart failure-related dataset GSE1145 was obtained from the Gene Expression Omnibus database. Differentially expressed genes were identified using R. A protein-protein interaction network of the differentially expressed genes was constructed using Search Tool for the Retrieval of Interacting Genes. The modules in each network were analyzed by Molecular Complex Detection of Cytoscape. The Database for Annotation, Visualization and Integrated Discovery was used to obtain the functions of the modules.

Results: Samples contained in GSE1145 were myocardial tissues from patients with dilated cardiomyopathy, familial cardiomyopathy, hypertrophic cardiomyopathy, ischemic cardiomyopathy, and post-partum cardiomyopathy. The differentially expressed genes, modules, and functions of the modules associated with different etiologies varied. Abnormal formation of extracellular matrix was overlapping among five etiologies. The change in cytoskeleton organization was specifically detected in dilated cardiomyopathy. The activation of the Wnt receptor signaling pathway was limited to hypertrophic cardiomyopathy. The change in nucleosome and chromatin assembly was associated with only familial cardiomyopathy. Germ cell migration and disrupted cellular calcium ion homeostasis were solely detected in ischemic cardiomyopathy. The change in the metabolic process of glucose and triglyceride was detected in only post-partum cardiomyopathy.

Conclusion: These results indicate that the pathogenesis of heart failure arising from different etiologies varies, which may provide molecular evidence supporting etiology-based treatment for heart failure patients.

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References
1.
Braunwald E . The war against heart failure: the Lancet lecture. Lancet. 2014; 385(9970):812-24. DOI: 10.1016/S0140-6736(14)61889-4. View

2.
Liao Y, Chen L, Huang R, Su P, Chan M, Chang C . Hypomethylation signature of tumor-initiating cells predicts poor prognosis of ovarian cancer patients. Hum Mol Genet. 2013; 23(7):1894-906. PMC: 3943526. DOI: 10.1093/hmg/ddt583. View

3.
Ayers D, Day P . Systems Medicine: The Application of Systems Biology Approaches for Modern Medical Research and Drug Development. Mol Biol Int. 2015; 2015:698169. PMC: 4556074. DOI: 10.1155/2015/698169. View

4.
Cowie M, Wood D, Coats A, Thompson S, Suresh V, Poole-Wilson P . Survival of patients with a new diagnosis of heart failure: a population based study. Heart. 2000; 83(5):505-10. PMC: 1760808. DOI: 10.1136/heart.83.5.505. View

5.
Lu D, Dong W, Zhang X, Quan X, Bao D, Lu Y . WIF1 causes dysfunction of heart in transgenic mice. Transgenic Res. 2013; 22(6):1179-89. PMC: 3835953. DOI: 10.1007/s11248-013-9738-z. View