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Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases

BACKGROUND: Identification of molecular classifiers from genome-wide gene expression analysis is an important practice for the investigation of biological systems in the post-genomic era - and one with great potential for near-term clinical impact. The 'Top-Scoring Pair' (TSP) classificati...

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Autores principales: Edelman, Lucas B, Toia, Giuseppe, Geman, Donald, Zhang, Wei, Price, Nathan D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797819/
https://www.ncbi.nlm.nih.gov/pubmed/19961616
http://dx.doi.org/10.1186/1471-2164-10-583
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author Edelman, Lucas B
Toia, Giuseppe
Geman, Donald
Zhang, Wei
Price, Nathan D
author_facet Edelman, Lucas B
Toia, Giuseppe
Geman, Donald
Zhang, Wei
Price, Nathan D
author_sort Edelman, Lucas B
collection PubMed
description BACKGROUND: Identification of molecular classifiers from genome-wide gene expression analysis is an important practice for the investigation of biological systems in the post-genomic era - and one with great potential for near-term clinical impact. The 'Top-Scoring Pair' (TSP) classification method identifies pairs of genes whose relative expression correlates strongly with phenotype. In this study, we sought to assess the effectiveness of the TSP approach in the identification of diagnostic classifiers for a number of human diseases including bacterial and viral infection, cardiomyopathy, diabetes, Crohn's disease, and transformed ulcerative colitis. We examined transcriptional profiles from both solid tissues and blood-borne leukocytes. RESULTS: The algorithm identified multiple predictive gene pairs for each phenotype, with cross-validation accuracy ranging from 70 to nearly 100 percent, and high sensitivity and specificity observed in most classification tasks. Performance compared favourably with that of pre-existing transcription-based classifiers, and in some cases was comparable to the accuracy of current clinical diagnostic procedures. Several diseases of solid tissues could be reliably diagnosed through classifiers based on the blood-borne leukocyte transcriptome. The TSP classifier thus represents a simple yet robust method to differentiate between diverse phenotypic states based on gene expression profiles. CONCLUSION: Two-transcript classifiers have the potential to reliably classify diverse human diseases, through analysis of both local diseased tissue and the immunological response assayed through blood-borne leukocytes. The experimental simplicity of this method results in measurements that can be easily translated to clinical practice.
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spelling pubmed-27978192009-12-25 Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases Edelman, Lucas B Toia, Giuseppe Geman, Donald Zhang, Wei Price, Nathan D BMC Genomics Research article BACKGROUND: Identification of molecular classifiers from genome-wide gene expression analysis is an important practice for the investigation of biological systems in the post-genomic era - and one with great potential for near-term clinical impact. The 'Top-Scoring Pair' (TSP) classification method identifies pairs of genes whose relative expression correlates strongly with phenotype. In this study, we sought to assess the effectiveness of the TSP approach in the identification of diagnostic classifiers for a number of human diseases including bacterial and viral infection, cardiomyopathy, diabetes, Crohn's disease, and transformed ulcerative colitis. We examined transcriptional profiles from both solid tissues and blood-borne leukocytes. RESULTS: The algorithm identified multiple predictive gene pairs for each phenotype, with cross-validation accuracy ranging from 70 to nearly 100 percent, and high sensitivity and specificity observed in most classification tasks. Performance compared favourably with that of pre-existing transcription-based classifiers, and in some cases was comparable to the accuracy of current clinical diagnostic procedures. Several diseases of solid tissues could be reliably diagnosed through classifiers based on the blood-borne leukocyte transcriptome. The TSP classifier thus represents a simple yet robust method to differentiate between diverse phenotypic states based on gene expression profiles. CONCLUSION: Two-transcript classifiers have the potential to reliably classify diverse human diseases, through analysis of both local diseased tissue and the immunological response assayed through blood-borne leukocytes. The experimental simplicity of this method results in measurements that can be easily translated to clinical practice. BioMed Central 2009-12-05 /pmc/articles/PMC2797819/ /pubmed/19961616 http://dx.doi.org/10.1186/1471-2164-10-583 Text en Copyright ©2009 Edelman 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
Edelman, Lucas B
Toia, Giuseppe
Geman, Donald
Zhang, Wei
Price, Nathan D
Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title_full Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title_fullStr Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title_full_unstemmed Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title_short Two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
title_sort two-transcript gene expression classifiers in the diagnosis and prognosis of human diseases
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797819/
https://www.ncbi.nlm.nih.gov/pubmed/19961616
http://dx.doi.org/10.1186/1471-2164-10-583
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