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An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression
BACKGROUND: Alzheimer's disease is a multifactorial disorder that may be diagnosed earlier using a combination of tests rather than any single test. Search algorithms and optimization techniques in combination with model evaluation techniques have been used previously to perform the selection o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682419/ https://www.ncbi.nlm.nih.gov/pubmed/26680269 http://dx.doi.org/10.1186/1471-2105-16-S18-S1 |
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author | Vandewater, Luke Brusic, Vladimir Wilson, William Macaulay, Lance Zhang, Ping |
author_facet | Vandewater, Luke Brusic, Vladimir Wilson, William Macaulay, Lance Zhang, Ping |
author_sort | Vandewater, Luke |
collection | PubMed |
description | BACKGROUND: Alzheimer's disease is a multifactorial disorder that may be diagnosed earlier using a combination of tests rather than any single test. Search algorithms and optimization techniques in combination with model evaluation techniques have been used previously to perform the selection of suitable feature sets. Previously we successfully applied GA with LR to neuropsychological data contained within the The Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging, to select cognitive tests for prediction of progression of AD. This research addresses an Adaptive Genetic Algorithm (AGA) in combination with LR for identifying the best biomarker combination for prediction of the progression to AD. RESULTS: The model has been explored in terms of parameter optimization to predict conversion from healthy stage to AD with high accuracy. Several feature sets were selected - the resulting prediction moddels showed higher area under the ROC values (0.83-0.89). The results has shown consistency with some of the medical research reported in literature. CONCLUSION: The AGA has proven useful in selecting the best combination of biomarkers for prediction of AD progression. The algorithm presented here is generic and can be extended to other data sets generated in projects that seek to identify combination of biomarkers or other features that are predictive of disease onset or progression. |
format | Online Article Text |
id | pubmed-4682419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46824192015-12-21 An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression Vandewater, Luke Brusic, Vladimir Wilson, William Macaulay, Lance Zhang, Ping BMC Bioinformatics Research BACKGROUND: Alzheimer's disease is a multifactorial disorder that may be diagnosed earlier using a combination of tests rather than any single test. Search algorithms and optimization techniques in combination with model evaluation techniques have been used previously to perform the selection of suitable feature sets. Previously we successfully applied GA with LR to neuropsychological data contained within the The Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging, to select cognitive tests for prediction of progression of AD. This research addresses an Adaptive Genetic Algorithm (AGA) in combination with LR for identifying the best biomarker combination for prediction of the progression to AD. RESULTS: The model has been explored in terms of parameter optimization to predict conversion from healthy stage to AD with high accuracy. Several feature sets were selected - the resulting prediction moddels showed higher area under the ROC values (0.83-0.89). The results has shown consistency with some of the medical research reported in literature. CONCLUSION: The AGA has proven useful in selecting the best combination of biomarkers for prediction of AD progression. The algorithm presented here is generic and can be extended to other data sets generated in projects that seek to identify combination of biomarkers or other features that are predictive of disease onset or progression. BioMed Central 2015-12-09 /pmc/articles/PMC4682419/ /pubmed/26680269 http://dx.doi.org/10.1186/1471-2105-16-S18-S1 Text en Copyright © 2015 Vandewater et al. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Vandewater, Luke Brusic, Vladimir Wilson, William Macaulay, Lance Zhang, Ping An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title | An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title_full | An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title_fullStr | An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title_full_unstemmed | An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title_short | An adaptive genetic algorithm for selection of blood-based biomarkers for prediction of Alzheimer's disease progression |
title_sort | adaptive genetic algorithm for selection of blood-based biomarkers for prediction of alzheimer's disease progression |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682419/ https://www.ncbi.nlm.nih.gov/pubmed/26680269 http://dx.doi.org/10.1186/1471-2105-16-S18-S1 |
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