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Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis

Alzheimer's Disease (AD) is the most common neurodegenerative disease in elderly people. Its development has been shown to be closely related to changes in the brain connectivity network and in the brain activation patterns along with structural changes caused by the neurodegenerative process....

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Autores principales: Ortiz, Andrés, Munilla, Jorge, Álvarez-Illán, Ignacio, Górriz, Juan M., Ramírez, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630314/
https://www.ncbi.nlm.nih.gov/pubmed/26578945
http://dx.doi.org/10.3389/fncom.2015.00132
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author Ortiz, Andrés
Munilla, Jorge
Álvarez-Illán, Ignacio
Górriz, Juan M.
Ramírez, Javier
author_facet Ortiz, Andrés
Munilla, Jorge
Álvarez-Illán, Ignacio
Górriz, Juan M.
Ramírez, Javier
author_sort Ortiz, Andrés
collection PubMed
description Alzheimer's Disease (AD) is the most common neurodegenerative disease in elderly people. Its development has been shown to be closely related to changes in the brain connectivity network and in the brain activation patterns along with structural changes caused by the neurodegenerative process. Methods to infer dependence between brain regions are usually derived from the analysis of covariance between activation levels in the different areas. However, these covariance-based methods are not able to estimate conditional independence between variables to factor out the influence of other regions. Conversely, models based on the inverse covariance, or precision matrix, such as Sparse Gaussian Graphical Models allow revealing conditional independence between regions by estimating the covariance between two variables given the rest as constant. This paper uses Sparse Inverse Covariance Estimation (SICE) methods to learn undirected graphs in order to derive functional and structural connectivity patterns from Fludeoxyglucose (18F-FDG) Position Emission Tomography (PET) data and segmented Magnetic Resonance images (MRI), drawn from the ADNI database, for Control, MCI (Mild Cognitive Impairment Subjects), and AD subjects. Sparse computation fits perfectly here as brain regions usually only interact with a few other areas. The models clearly show different metabolic covariation patters between subject groups, revealing the loss of strong connections in AD and MCI subjects when compared to Controls. Similarly, the variance between GM (Gray Matter) densities of different regions reveals different structural covariation patterns between the different groups. Thus, the different connectivity patterns for controls and AD are used in this paper to select regions of interest in PET and GM images with discriminative power for early AD diagnosis. Finally, functional an structural models are combined to leverage the classification accuracy. The results obtained in this work show the usefulness of the Sparse Gaussian Graphical models to reveal functional and structural connectivity patterns. This information provided by the sparse inverse covariance matrices is not only used in an exploratory way but we also propose a method to use it in a discriminative way. Regression coefficients are used to compute reconstruction errors for the different classes that are then introduced in a SVM for classification. Classification experiments performed using 68 Controls, 70 AD, and 111 MCI images and assessed by cross-validation show the effectiveness of the proposed method.
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spelling pubmed-46303142015-11-17 Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis Ortiz, Andrés Munilla, Jorge Álvarez-Illán, Ignacio Górriz, Juan M. Ramírez, Javier Front Comput Neurosci Neuroscience Alzheimer's Disease (AD) is the most common neurodegenerative disease in elderly people. Its development has been shown to be closely related to changes in the brain connectivity network and in the brain activation patterns along with structural changes caused by the neurodegenerative process. Methods to infer dependence between brain regions are usually derived from the analysis of covariance between activation levels in the different areas. However, these covariance-based methods are not able to estimate conditional independence between variables to factor out the influence of other regions. Conversely, models based on the inverse covariance, or precision matrix, such as Sparse Gaussian Graphical Models allow revealing conditional independence between regions by estimating the covariance between two variables given the rest as constant. This paper uses Sparse Inverse Covariance Estimation (SICE) methods to learn undirected graphs in order to derive functional and structural connectivity patterns from Fludeoxyglucose (18F-FDG) Position Emission Tomography (PET) data and segmented Magnetic Resonance images (MRI), drawn from the ADNI database, for Control, MCI (Mild Cognitive Impairment Subjects), and AD subjects. Sparse computation fits perfectly here as brain regions usually only interact with a few other areas. The models clearly show different metabolic covariation patters between subject groups, revealing the loss of strong connections in AD and MCI subjects when compared to Controls. Similarly, the variance between GM (Gray Matter) densities of different regions reveals different structural covariation patterns between the different groups. Thus, the different connectivity patterns for controls and AD are used in this paper to select regions of interest in PET and GM images with discriminative power for early AD diagnosis. Finally, functional an structural models are combined to leverage the classification accuracy. The results obtained in this work show the usefulness of the Sparse Gaussian Graphical models to reveal functional and structural connectivity patterns. This information provided by the sparse inverse covariance matrices is not only used in an exploratory way but we also propose a method to use it in a discriminative way. Regression coefficients are used to compute reconstruction errors for the different classes that are then introduced in a SVM for classification. Classification experiments performed using 68 Controls, 70 AD, and 111 MCI images and assessed by cross-validation show the effectiveness of the proposed method. Frontiers Media S.A. 2015-11-03 /pmc/articles/PMC4630314/ /pubmed/26578945 http://dx.doi.org/10.3389/fncom.2015.00132 Text en Copyright © 2015 Ortiz, Munilla, Álvarez-Illán, Górriz, Ramírez 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
Ortiz, Andrés
Munilla, Jorge
Álvarez-Illán, Ignacio
Górriz, Juan M.
Ramírez, Javier
Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title_full Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title_fullStr Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title_full_unstemmed Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title_short Exploratory graphical models of functional and structural connectivity patterns for Alzheimer's Disease diagnosis
title_sort exploratory graphical models of functional and structural connectivity patterns for alzheimer's disease diagnosis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630314/
https://www.ncbi.nlm.nih.gov/pubmed/26578945
http://dx.doi.org/10.3389/fncom.2015.00132
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