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Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging
The research on staging of pre-symptomatic and prodromal phase of neurological disorders, e.g., Alzheimer's disease (AD), is essential for prevention of dementia. New strategies for AD staging with a focus on early detection, are demanded to optimize potential efficacy of disease-modifying ther...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763344/ https://www.ncbi.nlm.nih.gov/pubmed/26941639 http://dx.doi.org/10.3389/fnagi.2016.00023 |
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author | Liu, Sidong Cai, Weidong Pujol, Sonia Kikinis, Ron Feng, Dagan D. |
author_facet | Liu, Sidong Cai, Weidong Pujol, Sonia Kikinis, Ron Feng, Dagan D. |
author_sort | Liu, Sidong |
collection | PubMed |
description | The research on staging of pre-symptomatic and prodromal phase of neurological disorders, e.g., Alzheimer's disease (AD), is essential for prevention of dementia. New strategies for AD staging with a focus on early detection, are demanded to optimize potential efficacy of disease-modifying therapies that can halt or slow the disease progression. Recently, neuroimaging are increasingly used as additional research-based markers to detect AD onset and predict conversion of MCI and normal control (NC) to AD. Researchers have proposed a variety of neuroimaging biomarkers to characterize the patterns of the pathology of AD and MCI, and suggested that multi-view neuroimaging biomarkers could lead to better performance than single-view biomarkers in AD staging. However, it is still unclear what leads to such synergy and how to preserve or maximize. In an attempt to answer these questions, we proposed a cross-view pattern analysis framework for investigating the synergy between different neuroimaging biomarkers. We quantitatively analyzed nine types of biomarkers derived from FDG-PET and T1-MRI, and evaluated their performance in a task of classifying AD, MCI, and NC subjects obtained from the ADNI baseline cohort. The experiment results showed that these biomarkers could depict the pathology of AD from different perspectives, and output distinct patterns that are significantly associated with the disease progression. Most importantly, we found that these features could be separated into clusters, each depicting a particular aspect; and the inter-cluster features could always achieve better performance than the intra-cluster features in AD staging. |
format | Online Article Text |
id | pubmed-4763344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47633442016-03-03 Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging Liu, Sidong Cai, Weidong Pujol, Sonia Kikinis, Ron Feng, Dagan D. Front Aging Neurosci Neuroscience The research on staging of pre-symptomatic and prodromal phase of neurological disorders, e.g., Alzheimer's disease (AD), is essential for prevention of dementia. New strategies for AD staging with a focus on early detection, are demanded to optimize potential efficacy of disease-modifying therapies that can halt or slow the disease progression. Recently, neuroimaging are increasingly used as additional research-based markers to detect AD onset and predict conversion of MCI and normal control (NC) to AD. Researchers have proposed a variety of neuroimaging biomarkers to characterize the patterns of the pathology of AD and MCI, and suggested that multi-view neuroimaging biomarkers could lead to better performance than single-view biomarkers in AD staging. However, it is still unclear what leads to such synergy and how to preserve or maximize. In an attempt to answer these questions, we proposed a cross-view pattern analysis framework for investigating the synergy between different neuroimaging biomarkers. We quantitatively analyzed nine types of biomarkers derived from FDG-PET and T1-MRI, and evaluated their performance in a task of classifying AD, MCI, and NC subjects obtained from the ADNI baseline cohort. The experiment results showed that these biomarkers could depict the pathology of AD from different perspectives, and output distinct patterns that are significantly associated with the disease progression. Most importantly, we found that these features could be separated into clusters, each depicting a particular aspect; and the inter-cluster features could always achieve better performance than the intra-cluster features in AD staging. Frontiers Media S.A. 2016-02-23 /pmc/articles/PMC4763344/ /pubmed/26941639 http://dx.doi.org/10.3389/fnagi.2016.00023 Text en Copyright © 2016 Liu, Cai, Pujol, Kikinis, Feng for the Alzheimer's Disease Neuroimaging Initiative. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Liu, Sidong Cai, Weidong Pujol, Sonia Kikinis, Ron Feng, Dagan D. Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title | Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title_full | Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title_fullStr | Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title_full_unstemmed | Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title_short | Cross-View Neuroimage Pattern Analysis in Alzheimer's Disease Staging |
title_sort | cross-view neuroimage pattern analysis in alzheimer's disease staging |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763344/ https://www.ncbi.nlm.nih.gov/pubmed/26941639 http://dx.doi.org/10.3389/fnagi.2016.00023 |
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