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Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment

INTRODUCTION: Currently, there are no tools that can accurately predict which patients with mild cognitive impairment (MCI) will progress to Alzheimer's disease (AD). Texture analysis uses image processing and statistical methods to identify patterns in voxel intensities that cannot be apprecia...

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Autores principales: Luk, Collin C., Ishaque, Abdullah, Khan, Muhammad, Ta, Daniel, Chenji, Sneha, Yang, Yee-Hong, Eurich, Dean, Kalra, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240791/
https://www.ncbi.nlm.nih.gov/pubmed/30480081
http://dx.doi.org/10.1016/j.dadm.2018.09.002
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author Luk, Collin C.
Ishaque, Abdullah
Khan, Muhammad
Ta, Daniel
Chenji, Sneha
Yang, Yee-Hong
Eurich, Dean
Kalra, Sanjay
author_facet Luk, Collin C.
Ishaque, Abdullah
Khan, Muhammad
Ta, Daniel
Chenji, Sneha
Yang, Yee-Hong
Eurich, Dean
Kalra, Sanjay
author_sort Luk, Collin C.
collection PubMed
description INTRODUCTION: Currently, there are no tools that can accurately predict which patients with mild cognitive impairment (MCI) will progress to Alzheimer's disease (AD). Texture analysis uses image processing and statistical methods to identify patterns in voxel intensities that cannot be appreciated by visual inspection. Our main objective was to determine whether MRI texture could be used to predict conversion of MCI to AD. METHODS: A method of 3-dimensional, whole-brain texture analysis was used to compute texture features from T1-weighted MR images. To assess predictive value, texture changes were compared between MCI converters and nonconverters over a 3-year observation period. A predictive model using texture and clinical factors was used to predict conversion of patients with MCI to AD. This model was then tested on ten randomly selected test groups from the data set. RESULTS: Texture features were found to be significantly different between normal controls (n = 225), patients with MCI (n = 382), and patients with AD (n = 183). A subset of the patients with MCI were used to compare between MCI converters (n = 98) and nonconverters (n = 106). A composite model including texture features, APOE-ε4 genotype, Mini-Mental Status Examination score, sex, and hippocampal occupancy resulted in an area under curve of 0.905. Application of the composite model to ten randomly selected test groups (nonconverters = 26, converters = 24) predicted MCI conversion with a mean accuracy of 76.2%. DISCUSSION: Early texture changes are detected in patients with MCI who eventually progress to AD dementia. Therefore, whole-brain 3D texture analysis has the potential to predict progression of patients with MCI to AD.
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spelling pubmed-62407912018-11-26 Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment Luk, Collin C. Ishaque, Abdullah Khan, Muhammad Ta, Daniel Chenji, Sneha Yang, Yee-Hong Eurich, Dean Kalra, Sanjay Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: Currently, there are no tools that can accurately predict which patients with mild cognitive impairment (MCI) will progress to Alzheimer's disease (AD). Texture analysis uses image processing and statistical methods to identify patterns in voxel intensities that cannot be appreciated by visual inspection. Our main objective was to determine whether MRI texture could be used to predict conversion of MCI to AD. METHODS: A method of 3-dimensional, whole-brain texture analysis was used to compute texture features from T1-weighted MR images. To assess predictive value, texture changes were compared between MCI converters and nonconverters over a 3-year observation period. A predictive model using texture and clinical factors was used to predict conversion of patients with MCI to AD. This model was then tested on ten randomly selected test groups from the data set. RESULTS: Texture features were found to be significantly different between normal controls (n = 225), patients with MCI (n = 382), and patients with AD (n = 183). A subset of the patients with MCI were used to compare between MCI converters (n = 98) and nonconverters (n = 106). A composite model including texture features, APOE-ε4 genotype, Mini-Mental Status Examination score, sex, and hippocampal occupancy resulted in an area under curve of 0.905. Application of the composite model to ten randomly selected test groups (nonconverters = 26, converters = 24) predicted MCI conversion with a mean accuracy of 76.2%. DISCUSSION: Early texture changes are detected in patients with MCI who eventually progress to AD dementia. Therefore, whole-brain 3D texture analysis has the potential to predict progression of patients with MCI to AD. Elsevier 2018-11-02 /pmc/articles/PMC6240791/ /pubmed/30480081 http://dx.doi.org/10.1016/j.dadm.2018.09.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroimaging
Luk, Collin C.
Ishaque, Abdullah
Khan, Muhammad
Ta, Daniel
Chenji, Sneha
Yang, Yee-Hong
Eurich, Dean
Kalra, Sanjay
Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title_full Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title_fullStr Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title_full_unstemmed Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title_short Alzheimer's disease: 3-Dimensional MRI texture for prediction of conversion from mild cognitive impairment
title_sort alzheimer's disease: 3-dimensional mri texture for prediction of conversion from mild cognitive impairment
topic Neuroimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240791/
https://www.ncbi.nlm.nih.gov/pubmed/30480081
http://dx.doi.org/10.1016/j.dadm.2018.09.002
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