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Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics

Group analysis in diffusion tensor imaging is challenging. Comparisons of tensor morphology across groups have typically been performed on scalar measures of diffusivity, such as fractional anisotropy (FA), disregarding the complex three-dimensional morphologies of diffusion tensors. Scalar measures...

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Autores principales: Metin, Mehmet Özer, Gökçay, Didem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019824/
https://www.ncbi.nlm.nih.gov/pubmed/33828445
http://dx.doi.org/10.3389/fnins.2021.625473
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author Metin, Mehmet Özer
Gökçay, Didem
author_facet Metin, Mehmet Özer
Gökçay, Didem
author_sort Metin, Mehmet Özer
collection PubMed
description Group analysis in diffusion tensor imaging is challenging. Comparisons of tensor morphology across groups have typically been performed on scalar measures of diffusivity, such as fractional anisotropy (FA), disregarding the complex three-dimensional morphologies of diffusion tensors. Scalar measures consider only the magnitude of the diffusion but not directions. In the present study, we have introduced a new approach based on directional statistics to use directional information of diffusion tensors in statistical group analysis based on Bingham distribution. We have investigated different directional statistical models to find the best fit. During the experiments, we confirmed that carrying out directional statistical analysis along the tract is much more effective than voxel- or skeleton-guided directional statistics. Hence, we propose a new method called tract profiling and directional statistics (TPDS) applicable to fiber bundles. As a case study, the method has been applied to identify connectivity differences of patients with major depressive disorder. The results obtained with the directional statistic-based analysis are consistent with those of NBS, but additionally, we found significant changes in the right hemisphere striatum, ACC, and prefrontal, parietal, temporal, and occipital connections as well as left hemispheric differences in the limbic areas such as the thalamus, amygdala, and hippocampus. The results are also evaluated with respect to fiber lengths. Comparison with the output of the network-based statistical toolbox indicated that the benefit of the proposed method becomes much more distinctive as the tract length increases. The likelihood of finding clusters of voxels that differ in long tracts is higher in TPDS, while that relationship is not clearly established in NBS.
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spelling pubmed-80198242021-04-06 Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics Metin, Mehmet Özer Gökçay, Didem Front Neurosci Neuroscience Group analysis in diffusion tensor imaging is challenging. Comparisons of tensor morphology across groups have typically been performed on scalar measures of diffusivity, such as fractional anisotropy (FA), disregarding the complex three-dimensional morphologies of diffusion tensors. Scalar measures consider only the magnitude of the diffusion but not directions. In the present study, we have introduced a new approach based on directional statistics to use directional information of diffusion tensors in statistical group analysis based on Bingham distribution. We have investigated different directional statistical models to find the best fit. During the experiments, we confirmed that carrying out directional statistical analysis along the tract is much more effective than voxel- or skeleton-guided directional statistics. Hence, we propose a new method called tract profiling and directional statistics (TPDS) applicable to fiber bundles. As a case study, the method has been applied to identify connectivity differences of patients with major depressive disorder. The results obtained with the directional statistic-based analysis are consistent with those of NBS, but additionally, we found significant changes in the right hemisphere striatum, ACC, and prefrontal, parietal, temporal, and occipital connections as well as left hemispheric differences in the limbic areas such as the thalamus, amygdala, and hippocampus. The results are also evaluated with respect to fiber lengths. Comparison with the output of the network-based statistical toolbox indicated that the benefit of the proposed method becomes much more distinctive as the tract length increases. The likelihood of finding clusters of voxels that differ in long tracts is higher in TPDS, while that relationship is not clearly established in NBS. Frontiers Media S.A. 2021-03-22 /pmc/articles/PMC8019824/ /pubmed/33828445 http://dx.doi.org/10.3389/fnins.2021.625473 Text en Copyright © 2021 Metin and Gökçay. 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 Neuroscience
Metin, Mehmet Özer
Gökçay, Didem
Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title_full Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title_fullStr Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title_full_unstemmed Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title_short Diffusion Tensor Imaging Group Analysis Using Tract Profiling and Directional Statistics
title_sort diffusion tensor imaging group analysis using tract profiling and directional statistics
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019824/
https://www.ncbi.nlm.nih.gov/pubmed/33828445
http://dx.doi.org/10.3389/fnins.2021.625473
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