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A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities
Relating disease status to imaging data stands to increase the clinical significance of neuroimaging studies. Many neurological and psychiatric disorders involve complex, systems-level alterations that manifest in functional and structural properties of the brain and possibly other clinical and biol...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879954/ https://www.ncbi.nlm.nih.gov/pubmed/29632471 http://dx.doi.org/10.3389/fnins.2018.00184 |
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author | Xue, Wenqiong Bowman, F. DuBois Kang, Jian |
author_facet | Xue, Wenqiong Bowman, F. DuBois Kang, Jian |
author_sort | Xue, Wenqiong |
collection | PubMed |
description | Relating disease status to imaging data stands to increase the clinical significance of neuroimaging studies. Many neurological and psychiatric disorders involve complex, systems-level alterations that manifest in functional and structural properties of the brain and possibly other clinical and biologic measures. We propose a Bayesian hierarchical model to predict disease status, which is able to incorporate information from both functional and structural brain imaging scans. We consider a two-stage whole brain parcellation, partitioning the brain into 282 subregions, and our model accounts for correlations between voxels from different brain regions defined by the parcellations. Our approach models the imaging data and uses posterior predictive probabilities to perform prediction. The estimates of our model parameters are based on samples drawn from the joint posterior distribution using Markov Chain Monte Carlo (MCMC) methods. We evaluate our method by examining the prediction accuracy rates based on leave-one-out cross validation, and we employ an importance sampling strategy to reduce the computation time. We conduct both whole-brain and voxel-level prediction and identify the brain regions that are highly associated with the disease based on the voxel-level prediction results. We apply our model to multimodal brain imaging data from a study of Parkinson's disease. We achieve extremely high accuracy, in general, and our model identifies key regions contributing to accurate prediction including caudate, putamen, and fusiform gyrus as well as several sensory system regions. |
format | Online Article Text |
id | pubmed-5879954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58799542018-04-09 A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities Xue, Wenqiong Bowman, F. DuBois Kang, Jian Front Neurosci Neuroscience Relating disease status to imaging data stands to increase the clinical significance of neuroimaging studies. Many neurological and psychiatric disorders involve complex, systems-level alterations that manifest in functional and structural properties of the brain and possibly other clinical and biologic measures. We propose a Bayesian hierarchical model to predict disease status, which is able to incorporate information from both functional and structural brain imaging scans. We consider a two-stage whole brain parcellation, partitioning the brain into 282 subregions, and our model accounts for correlations between voxels from different brain regions defined by the parcellations. Our approach models the imaging data and uses posterior predictive probabilities to perform prediction. The estimates of our model parameters are based on samples drawn from the joint posterior distribution using Markov Chain Monte Carlo (MCMC) methods. We evaluate our method by examining the prediction accuracy rates based on leave-one-out cross validation, and we employ an importance sampling strategy to reduce the computation time. We conduct both whole-brain and voxel-level prediction and identify the brain regions that are highly associated with the disease based on the voxel-level prediction results. We apply our model to multimodal brain imaging data from a study of Parkinson's disease. We achieve extremely high accuracy, in general, and our model identifies key regions contributing to accurate prediction including caudate, putamen, and fusiform gyrus as well as several sensory system regions. Frontiers Media S.A. 2018-03-26 /pmc/articles/PMC5879954/ /pubmed/29632471 http://dx.doi.org/10.3389/fnins.2018.00184 Text en Copyright © 2018 Xue, Bowman and Kang. 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 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 Xue, Wenqiong Bowman, F. DuBois Kang, Jian A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title | A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title_full | A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title_fullStr | A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title_full_unstemmed | A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title_short | A Bayesian Spatial Model to Predict Disease Status Using Imaging Data From Various Modalities |
title_sort | bayesian spatial model to predict disease status using imaging data from various modalities |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879954/ https://www.ncbi.nlm.nih.gov/pubmed/29632471 http://dx.doi.org/10.3389/fnins.2018.00184 |
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