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A comparative study of discriminating human heart failure etiology using gene expression profiles
BACKGROUND: Human heart failure is a complex disease that manifests from multiple genetic and environmental factors. Although ischemic and non-ischemic heart disease present clinically with many similar decreases in ventricular function, emerging work suggests that they are distinct diseases with di...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1224853/ https://www.ncbi.nlm.nih.gov/pubmed/16120216 http://dx.doi.org/10.1186/1471-2105-6-205 |
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author | Huang, Xiaohong Pan, Wei Grindle, Suzanne Han, Xinqiang Chen, Yingjie Park, Soon J Miller, Leslie W Hall, Jennifer |
author_facet | Huang, Xiaohong Pan, Wei Grindle, Suzanne Han, Xinqiang Chen, Yingjie Park, Soon J Miller, Leslie W Hall, Jennifer |
author_sort | Huang, Xiaohong |
collection | PubMed |
description | BACKGROUND: Human heart failure is a complex disease that manifests from multiple genetic and environmental factors. Although ischemic and non-ischemic heart disease present clinically with many similar decreases in ventricular function, emerging work suggests that they are distinct diseases with different responses to therapy. The ability to distinguish between ischemic and non-ischemic heart failure may be essential to guide appropriate therapy and determine prognosis for successful treatment. In this paper we consider discriminating the etiologies of heart failure using gene expression libraries from two separate institutions. RESULTS: We apply five new statistical methods, including partial least squares, penalized partial least squares, LASSO, nearest shrunken centroids and random forest, to two real datasets and compare their performance for multiclass classification. It is found that the five statistical methods perform similarly on each of the two datasets: it is difficult to correctly distinguish the etiologies of heart failure in one dataset whereas it is easy for the other one. In a simulation study, it is confirmed that the five methods tend to have close performance, though the random forest seems to have a slight edge. CONCLUSIONS: For some gene expression data, several recently developed discriminant methods may perform similarly. More importantly, one must remain cautious when assessing the discriminating performance using gene expression profiles based on a small dataset; our analysis suggests the importance of utilizing multiple or larger datasets. |
format | Text |
id | pubmed-1224853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-12248532005-09-22 A comparative study of discriminating human heart failure etiology using gene expression profiles Huang, Xiaohong Pan, Wei Grindle, Suzanne Han, Xinqiang Chen, Yingjie Park, Soon J Miller, Leslie W Hall, Jennifer BMC Bioinformatics Research Article BACKGROUND: Human heart failure is a complex disease that manifests from multiple genetic and environmental factors. Although ischemic and non-ischemic heart disease present clinically with many similar decreases in ventricular function, emerging work suggests that they are distinct diseases with different responses to therapy. The ability to distinguish between ischemic and non-ischemic heart failure may be essential to guide appropriate therapy and determine prognosis for successful treatment. In this paper we consider discriminating the etiologies of heart failure using gene expression libraries from two separate institutions. RESULTS: We apply five new statistical methods, including partial least squares, penalized partial least squares, LASSO, nearest shrunken centroids and random forest, to two real datasets and compare their performance for multiclass classification. It is found that the five statistical methods perform similarly on each of the two datasets: it is difficult to correctly distinguish the etiologies of heart failure in one dataset whereas it is easy for the other one. In a simulation study, it is confirmed that the five methods tend to have close performance, though the random forest seems to have a slight edge. CONCLUSIONS: For some gene expression data, several recently developed discriminant methods may perform similarly. More importantly, one must remain cautious when assessing the discriminating performance using gene expression profiles based on a small dataset; our analysis suggests the importance of utilizing multiple or larger datasets. BioMed Central 2005-08-24 /pmc/articles/PMC1224853/ /pubmed/16120216 http://dx.doi.org/10.1186/1471-2105-6-205 Text en Copyright © 2005 Huang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Huang, Xiaohong Pan, Wei Grindle, Suzanne Han, Xinqiang Chen, Yingjie Park, Soon J Miller, Leslie W Hall, Jennifer A comparative study of discriminating human heart failure etiology using gene expression profiles |
title | A comparative study of discriminating human heart failure etiology using gene expression profiles |
title_full | A comparative study of discriminating human heart failure etiology using gene expression profiles |
title_fullStr | A comparative study of discriminating human heart failure etiology using gene expression profiles |
title_full_unstemmed | A comparative study of discriminating human heart failure etiology using gene expression profiles |
title_short | A comparative study of discriminating human heart failure etiology using gene expression profiles |
title_sort | comparative study of discriminating human heart failure etiology using gene expression profiles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1224853/ https://www.ncbi.nlm.nih.gov/pubmed/16120216 http://dx.doi.org/10.1186/1471-2105-6-205 |
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