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Investigating white matter fibre density and morphology using fixel-based analysis

Voxel-based analysis of diffusion MRI data is increasingly popular. However, most white matter voxels contain contributions from multiple fibre populations (often referred to as crossing fibres), and therefore voxel-averaged quantitative measures (e.g. fractional anisotropy) are not fibre-specific a...

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Autores principales: Raffelt, David A., Tournier, J.-Donald, Smith, Robert E., Vaughan, David N., Jackson, Graeme, Ridgway, Gerard R., Connelly, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5182031/
https://www.ncbi.nlm.nih.gov/pubmed/27639350
http://dx.doi.org/10.1016/j.neuroimage.2016.09.029
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author Raffelt, David A.
Tournier, J.-Donald
Smith, Robert E.
Vaughan, David N.
Jackson, Graeme
Ridgway, Gerard R.
Connelly, Alan
author_facet Raffelt, David A.
Tournier, J.-Donald
Smith, Robert E.
Vaughan, David N.
Jackson, Graeme
Ridgway, Gerard R.
Connelly, Alan
author_sort Raffelt, David A.
collection PubMed
description Voxel-based analysis of diffusion MRI data is increasingly popular. However, most white matter voxels contain contributions from multiple fibre populations (often referred to as crossing fibres), and therefore voxel-averaged quantitative measures (e.g. fractional anisotropy) are not fibre-specific and have poor interpretability. Using higher-order diffusion models, parameters related to fibre density can be extracted for individual fibre populations within each voxel (‘fixels’), and recent advances in statistics enable the multi-subject analysis of such data. However, investigating within-voxel microscopic fibre density alone does not account for macroscopic differences in the white matter morphology (e.g. the calibre of a fibre bundle). In this work, we introduce a novel method to investigate the latter, which we call fixel-based morphometry (FBM). To obtain a more complete measure related to the total number of white matter axons, information from both within-voxel microscopic fibre density and macroscopic morphology must be combined. We therefore present the FBM method as an integral piece within a comprehensive fixel-based analysis framework to investigate measures of fibre density, fibre-bundle morphology (cross-section), and a combined measure of fibre density and cross-section. We performed simulations to demonstrate the proposed measures using various transformations of a numerical fibre bundle phantom. Finally, we provide an example of such an analysis by comparing a clinical patient group to a healthy control group, which demonstrates that all three measures provide distinct and complementary information. By capturing information from both sources, the combined fibre density and cross-section measure is likely to be more sensitive to certain pathologies and more directly interpretable.
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spelling pubmed-51820312017-01-03 Investigating white matter fibre density and morphology using fixel-based analysis Raffelt, David A. Tournier, J.-Donald Smith, Robert E. Vaughan, David N. Jackson, Graeme Ridgway, Gerard R. Connelly, Alan Neuroimage Article Voxel-based analysis of diffusion MRI data is increasingly popular. However, most white matter voxels contain contributions from multiple fibre populations (often referred to as crossing fibres), and therefore voxel-averaged quantitative measures (e.g. fractional anisotropy) are not fibre-specific and have poor interpretability. Using higher-order diffusion models, parameters related to fibre density can be extracted for individual fibre populations within each voxel (‘fixels’), and recent advances in statistics enable the multi-subject analysis of such data. However, investigating within-voxel microscopic fibre density alone does not account for macroscopic differences in the white matter morphology (e.g. the calibre of a fibre bundle). In this work, we introduce a novel method to investigate the latter, which we call fixel-based morphometry (FBM). To obtain a more complete measure related to the total number of white matter axons, information from both within-voxel microscopic fibre density and macroscopic morphology must be combined. We therefore present the FBM method as an integral piece within a comprehensive fixel-based analysis framework to investigate measures of fibre density, fibre-bundle morphology (cross-section), and a combined measure of fibre density and cross-section. We performed simulations to demonstrate the proposed measures using various transformations of a numerical fibre bundle phantom. Finally, we provide an example of such an analysis by comparing a clinical patient group to a healthy control group, which demonstrates that all three measures provide distinct and complementary information. By capturing information from both sources, the combined fibre density and cross-section measure is likely to be more sensitive to certain pathologies and more directly interpretable. Academic Press 2017-01-01 /pmc/articles/PMC5182031/ /pubmed/27639350 http://dx.doi.org/10.1016/j.neuroimage.2016.09.029 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Raffelt, David A.
Tournier, J.-Donald
Smith, Robert E.
Vaughan, David N.
Jackson, Graeme
Ridgway, Gerard R.
Connelly, Alan
Investigating white matter fibre density and morphology using fixel-based analysis
title Investigating white matter fibre density and morphology using fixel-based analysis
title_full Investigating white matter fibre density and morphology using fixel-based analysis
title_fullStr Investigating white matter fibre density and morphology using fixel-based analysis
title_full_unstemmed Investigating white matter fibre density and morphology using fixel-based analysis
title_short Investigating white matter fibre density and morphology using fixel-based analysis
title_sort investigating white matter fibre density and morphology using fixel-based analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5182031/
https://www.ncbi.nlm.nih.gov/pubmed/27639350
http://dx.doi.org/10.1016/j.neuroimage.2016.09.029
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