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Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI

Accurate prediction of the early stage of Alzheimer's disease (AD) is important but very challenging. The goal of this study was to utilize predictors for diagnosis conversion to AD based on integrating resting-state functional MRI (rs-fMRI) connectivity analysis and structural MRI (sMRI). We i...

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Autores principales: Hojjati, Seyed Hani, Ebrahimzadeh, Ata, Babajani-Feremi, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730495/
https://www.ncbi.nlm.nih.gov/pubmed/31543860
http://dx.doi.org/10.3389/fneur.2019.00904
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author Hojjati, Seyed Hani
Ebrahimzadeh, Ata
Babajani-Feremi, Abbas
author_facet Hojjati, Seyed Hani
Ebrahimzadeh, Ata
Babajani-Feremi, Abbas
author_sort Hojjati, Seyed Hani
collection PubMed
description Accurate prediction of the early stage of Alzheimer's disease (AD) is important but very challenging. The goal of this study was to utilize predictors for diagnosis conversion to AD based on integrating resting-state functional MRI (rs-fMRI) connectivity analysis and structural MRI (sMRI). We included 177 subjects in this study and aimed at identifying patients with mild cognitive impairment (MCI) who progress to AD, MCI converter (MCI-C), patients with MCI who do not progress to AD, MCI non-converter (MCI-NC), patients with AD, and healthy controls (HC). The graph theory was used to characterize different aspects of the rs-fMRI brain network by calculating measures of integration and segregation. The cortical and subcortical measurements, e.g., cortical thickness, were extracted from sMRI data. The rs-fMRI graph measures were combined with the sMRI measures to construct input features of a support vector machine (SVM) and classify different groups of subjects. Two feature selection algorithms [i.e., the discriminant correlation analysis (DCA) and sequential feature collection (SFC)] were used for feature reduction and selecting a subset of optimal features. Maximum accuracy of 67 and 56% for three-group (“AD, MCI-C, and MCI-NC” or “MCI-C, MCI-NC, and HC”) and four-group (“AD, MCI-C, MCI-NC, and HC”) classification, respectively, were obtained with the SFC feature selection algorithm. We also identified hub nodes in the rs-fMRI brain network which were associated with the early stage of AD. Our results demonstrated the potential of the proposed method based on integration of the functional and structural MRI for identification of the early stage of AD.
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spelling pubmed-67304952019-09-20 Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI Hojjati, Seyed Hani Ebrahimzadeh, Ata Babajani-Feremi, Abbas Front Neurol Neurology Accurate prediction of the early stage of Alzheimer's disease (AD) is important but very challenging. The goal of this study was to utilize predictors for diagnosis conversion to AD based on integrating resting-state functional MRI (rs-fMRI) connectivity analysis and structural MRI (sMRI). We included 177 subjects in this study and aimed at identifying patients with mild cognitive impairment (MCI) who progress to AD, MCI converter (MCI-C), patients with MCI who do not progress to AD, MCI non-converter (MCI-NC), patients with AD, and healthy controls (HC). The graph theory was used to characterize different aspects of the rs-fMRI brain network by calculating measures of integration and segregation. The cortical and subcortical measurements, e.g., cortical thickness, were extracted from sMRI data. The rs-fMRI graph measures were combined with the sMRI measures to construct input features of a support vector machine (SVM) and classify different groups of subjects. Two feature selection algorithms [i.e., the discriminant correlation analysis (DCA) and sequential feature collection (SFC)] were used for feature reduction and selecting a subset of optimal features. Maximum accuracy of 67 and 56% for three-group (“AD, MCI-C, and MCI-NC” or “MCI-C, MCI-NC, and HC”) and four-group (“AD, MCI-C, MCI-NC, and HC”) classification, respectively, were obtained with the SFC feature selection algorithm. We also identified hub nodes in the rs-fMRI brain network which were associated with the early stage of AD. Our results demonstrated the potential of the proposed method based on integration of the functional and structural MRI for identification of the early stage of AD. Frontiers Media S.A. 2019-08-30 /pmc/articles/PMC6730495/ /pubmed/31543860 http://dx.doi.org/10.3389/fneur.2019.00904 Text en Copyright © 2019 Hojjati, Ebrahimzadeh and Babajani-Feremi. 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) and the copyright owner(s) 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 Neurology
Hojjati, Seyed Hani
Ebrahimzadeh, Ata
Babajani-Feremi, Abbas
Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title_full Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title_fullStr Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title_full_unstemmed Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title_short Identification of the Early Stage of Alzheimer's Disease Using Structural MRI and Resting-State fMRI
title_sort identification of the early stage of alzheimer's disease using structural mri and resting-state fmri
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730495/
https://www.ncbi.nlm.nih.gov/pubmed/31543860
http://dx.doi.org/10.3389/fneur.2019.00904
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