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Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI
OBJECTIVE: This study proposes an automated diagnostic method to classify patients with Alzheimer's disease (AD) of degenerative etiology using magnetic resonance imaging (MRI) markers. METHODS: Twenty-seven patients with subjective memory impairment (SMI), 18 patients with mild cognitive impai...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neuropsychiatric Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310927/ https://www.ncbi.nlm.nih.gov/pubmed/25670951 http://dx.doi.org/10.4306/pi.2015.12.1.92 |
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author | Jung, Won Beom Lee, Young Min Kim, Young Hoon Mun, Chi-Woong |
author_facet | Jung, Won Beom Lee, Young Min Kim, Young Hoon Mun, Chi-Woong |
author_sort | Jung, Won Beom |
collection | PubMed |
description | OBJECTIVE: This study proposes an automated diagnostic method to classify patients with Alzheimer's disease (AD) of degenerative etiology using magnetic resonance imaging (MRI) markers. METHODS: Twenty-seven patients with subjective memory impairment (SMI), 18 patients with mild cognitive impairment (MCI), and 27 patients with AD participated. MRI protocols included three dimensional brain structural imaging and diffusion tensor imaging to assess the cortical thickness, subcortical volume and white matter integrity. Recursive feature elimination based on support vector machine (SVM) was conducted to determine the most relevant features for classifying abnormal regions and imaging parameters, and then a factor analysis for the top-ranked factors was performed. Subjects were classified using nonlinear SVM. RESULTS: Medial temporal regions in AD patients were dominantly detected with cortical thinning and volume atrophy compared with SMI and MCI patients. Damage to white matter integrity was also accredited with decreased fractional anisotropy and increased mean diffusivity (MD) across the three groups. The microscopic damage in the subcortical gray matter was reflected in increased MD. Classification accuracy between pairs of groups (SMI vs. MCI, MCI vs. AD, SMI vs. AD) and among all three groups were 84.4% (±13.8), 86.9% (±10.5), 96.3% (±4.6), and 70.5% (±11.5), respectively. CONCLUSION: This proposed method may be a potential tool to diagnose AD pathology with the current clinical criteria. |
format | Online Article Text |
id | pubmed-4310927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-43109272015-02-10 Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI Jung, Won Beom Lee, Young Min Kim, Young Hoon Mun, Chi-Woong Psychiatry Investig Original Article OBJECTIVE: This study proposes an automated diagnostic method to classify patients with Alzheimer's disease (AD) of degenerative etiology using magnetic resonance imaging (MRI) markers. METHODS: Twenty-seven patients with subjective memory impairment (SMI), 18 patients with mild cognitive impairment (MCI), and 27 patients with AD participated. MRI protocols included three dimensional brain structural imaging and diffusion tensor imaging to assess the cortical thickness, subcortical volume and white matter integrity. Recursive feature elimination based on support vector machine (SVM) was conducted to determine the most relevant features for classifying abnormal regions and imaging parameters, and then a factor analysis for the top-ranked factors was performed. Subjects were classified using nonlinear SVM. RESULTS: Medial temporal regions in AD patients were dominantly detected with cortical thinning and volume atrophy compared with SMI and MCI patients. Damage to white matter integrity was also accredited with decreased fractional anisotropy and increased mean diffusivity (MD) across the three groups. The microscopic damage in the subcortical gray matter was reflected in increased MD. Classification accuracy between pairs of groups (SMI vs. MCI, MCI vs. AD, SMI vs. AD) and among all three groups were 84.4% (±13.8), 86.9% (±10.5), 96.3% (±4.6), and 70.5% (±11.5), respectively. CONCLUSION: This proposed method may be a potential tool to diagnose AD pathology with the current clinical criteria. Korean Neuropsychiatric Association 2015-01 2015-01-12 /pmc/articles/PMC4310927/ /pubmed/25670951 http://dx.doi.org/10.4306/pi.2015.12.1.92 Text en Copyright © 2015 Korean Neuropsychiatric Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jung, Won Beom Lee, Young Min Kim, Young Hoon Mun, Chi-Woong Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title | Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title_full | Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title_fullStr | Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title_full_unstemmed | Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title_short | Automated Classification to Predict the Progression of Alzheimer's Disease Using Whole-Brain Volumetry and DTI |
title_sort | automated classification to predict the progression of alzheimer's disease using whole-brain volumetry and dti |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310927/ https://www.ncbi.nlm.nih.gov/pubmed/25670951 http://dx.doi.org/10.4306/pi.2015.12.1.92 |
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