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Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset

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. M...

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Autores principales: Yang, Guodong, Chen, Shuping, Ma, Aiqun, Lu, Jun, Wang, Tingzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666440/
https://www.ncbi.nlm.nih.gov/pubmed/29160422
http://dx.doi.org/10.6061/clinics/2017(10)03
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author Yang, Guodong
Chen, Shuping
Ma, Aiqun
Lu, Jun
Wang, Tingzhong
author_facet Yang, Guodong
Chen, Shuping
Ma, Aiqun
Lu, Jun
Wang, Tingzhong
author_sort Yang, Guodong
collection PubMed
description 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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spelling pubmed-56664402017-11-07 Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset Yang, Guodong Chen, Shuping Ma, Aiqun Lu, Jun Wang, Tingzhong Clinics (Sao Paulo) Clinical Science 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. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2017-10 2017-10 /pmc/articles/PMC5666440/ /pubmed/29160422 http://dx.doi.org/10.6061/clinics/2017(10)03 Text en Copyright © 2017 CLINICS http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.
spellingShingle Clinical Science
Yang, Guodong
Chen, Shuping
Ma, Aiqun
Lu, Jun
Wang, Tingzhong
Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title_full Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title_fullStr Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title_full_unstemmed Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title_short Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
title_sort identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666440/
https://www.ncbi.nlm.nih.gov/pubmed/29160422
http://dx.doi.org/10.6061/clinics/2017(10)03
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