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Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals

BACKGROUND: Accurate parcellation of the cerebral cortex in an individual is a guide to its underlying organization. The most promising in vivo quantitative magnetic resonance (MR)-based microstructural cortical mapping methods are yet to achieve a level of parcellation accuracy comparable to quanti...

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Autores principales: Moinian, Shahrzad, Vegh, Viktor, Reutens, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977388/
https://www.ncbi.nlm.nih.gov/pubmed/35483706
http://dx.doi.org/10.1093/cercor/bhac155
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author Moinian, Shahrzad
Vegh, Viktor
Reutens, David
author_facet Moinian, Shahrzad
Vegh, Viktor
Reutens, David
author_sort Moinian, Shahrzad
collection PubMed
description BACKGROUND: Accurate parcellation of the cerebral cortex in an individual is a guide to its underlying organization. The most promising in vivo quantitative magnetic resonance (MR)-based microstructural cortical mapping methods are yet to achieve a level of parcellation accuracy comparable to quantitative histology. METHODS: We scanned 6 participants using a 3D echo-planar imaging MR fingerprinting (EPI-MRF) sequence on a 7T Siemens scanner. After projecting MRF signals to the individual-specific inflated model of the cortical surface, normalized autocorrelations of MRF residuals of vertices of 8 microstructurally distinct areas (BA1, BA2, BA4a, BA6, BA44, BA45, BA17, and BA18) from 3 cortical regions were used as feature vector inputs into linear support vector machine (SVM), radial basis function SVM (RBF-SVM), random forest, and k-nearest neighbors supervised classification algorithms. The algorithms' prediction performance was compared using: (i) features from each vertex or (ii) features from neighboring vertices. RESULTS: The neighborhood-based RBF-SVM classifier achieved the highest prediction score of 0.85 for classification of MRF residuals in the central region from a held-out participant. CONCLUSIONS: We developed an automated method of cortical parcellation using a combination of MR fingerprinting residual analysis and machine learning classification. Our findings provide the basis for employing unsupervised learning algorithms for whole-cortex structural parcellation in individuals.
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spelling pubmed-99773882023-03-02 Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals Moinian, Shahrzad Vegh, Viktor Reutens, David Cereb Cortex Original Article BACKGROUND: Accurate parcellation of the cerebral cortex in an individual is a guide to its underlying organization. The most promising in vivo quantitative magnetic resonance (MR)-based microstructural cortical mapping methods are yet to achieve a level of parcellation accuracy comparable to quantitative histology. METHODS: We scanned 6 participants using a 3D echo-planar imaging MR fingerprinting (EPI-MRF) sequence on a 7T Siemens scanner. After projecting MRF signals to the individual-specific inflated model of the cortical surface, normalized autocorrelations of MRF residuals of vertices of 8 microstructurally distinct areas (BA1, BA2, BA4a, BA6, BA44, BA45, BA17, and BA18) from 3 cortical regions were used as feature vector inputs into linear support vector machine (SVM), radial basis function SVM (RBF-SVM), random forest, and k-nearest neighbors supervised classification algorithms. The algorithms' prediction performance was compared using: (i) features from each vertex or (ii) features from neighboring vertices. RESULTS: The neighborhood-based RBF-SVM classifier achieved the highest prediction score of 0.85 for classification of MRF residuals in the central region from a held-out participant. CONCLUSIONS: We developed an automated method of cortical parcellation using a combination of MR fingerprinting residual analysis and machine learning classification. Our findings provide the basis for employing unsupervised learning algorithms for whole-cortex structural parcellation in individuals. Oxford University Press 2022-04-28 /pmc/articles/PMC9977388/ /pubmed/35483706 http://dx.doi.org/10.1093/cercor/bhac155 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Moinian, Shahrzad
Vegh, Viktor
Reutens, David
Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title_full Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title_fullStr Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title_full_unstemmed Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title_short Towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
title_sort towards automated in vivo parcellation of the human cerebral cortex using supervised classification of magnetic resonance fingerprinting residuals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977388/
https://www.ncbi.nlm.nih.gov/pubmed/35483706
http://dx.doi.org/10.1093/cercor/bhac155
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