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Differential Development of Human Brain White Matter Tracts

Neuroscience is increasingly focusing on developmental factors related to human structural and functional connectivity. Unfortunately, to date, diffusion-based imaging approaches have only contributed modestly to these broad objectives, despite the promise of diffusion-based tractography. Here, we r...

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Autores principales: Imperati, Davide, Colcombe, Stan, Kelly, Clare, Di Martino, Adriana, Zhou, Juan, Castellanos, F. Xavier, Milham, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166135/
https://www.ncbi.nlm.nih.gov/pubmed/21909351
http://dx.doi.org/10.1371/journal.pone.0023437
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author Imperati, Davide
Colcombe, Stan
Kelly, Clare
Di Martino, Adriana
Zhou, Juan
Castellanos, F. Xavier
Milham, Michael P.
author_facet Imperati, Davide
Colcombe, Stan
Kelly, Clare
Di Martino, Adriana
Zhou, Juan
Castellanos, F. Xavier
Milham, Michael P.
author_sort Imperati, Davide
collection PubMed
description Neuroscience is increasingly focusing on developmental factors related to human structural and functional connectivity. Unfortunately, to date, diffusion-based imaging approaches have only contributed modestly to these broad objectives, despite the promise of diffusion-based tractography. Here, we report a novel data-driven approach to detect similarities and differences among white matter tracts with respect to their developmental trajectories, using 64-direction diffusion tensor imaging. Specifically, using a cross-sectional sample comprising 144 healthy individuals (7 to 48 years old), we applied k-means cluster analysis to separate white matter voxels based on their age-related trajectories of fractional anisotropy. Optimal solutions included 5-, 9- and 14-clusters. Our results recapitulate well-established tracts (e.g., internal and external capsule, optic radiations, corpus callosum, cingulum bundle, cerebral peduncles) and subdivisions within tracts (e.g., corpus callosum, internal capsule). For all but one tract identified, age-related trajectories were curvilinear (i.e., inverted ‘U-shape’), with age-related increases during childhood and adolescence followed by decreases in middle adulthood. Identification of peaks in the trajectories suggests that age-related losses in fractional anisotropy occur as early as 23 years of age, with mean onset at 30 years of age. Our findings demonstrate that data-driven analytic techniques may be fruitfully applied to extant diffusion tensor imaging datasets in normative and neuropsychiatric samples.
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spelling pubmed-31661352011-09-09 Differential Development of Human Brain White Matter Tracts Imperati, Davide Colcombe, Stan Kelly, Clare Di Martino, Adriana Zhou, Juan Castellanos, F. Xavier Milham, Michael P. PLoS One Research Article Neuroscience is increasingly focusing on developmental factors related to human structural and functional connectivity. Unfortunately, to date, diffusion-based imaging approaches have only contributed modestly to these broad objectives, despite the promise of diffusion-based tractography. Here, we report a novel data-driven approach to detect similarities and differences among white matter tracts with respect to their developmental trajectories, using 64-direction diffusion tensor imaging. Specifically, using a cross-sectional sample comprising 144 healthy individuals (7 to 48 years old), we applied k-means cluster analysis to separate white matter voxels based on their age-related trajectories of fractional anisotropy. Optimal solutions included 5-, 9- and 14-clusters. Our results recapitulate well-established tracts (e.g., internal and external capsule, optic radiations, corpus callosum, cingulum bundle, cerebral peduncles) and subdivisions within tracts (e.g., corpus callosum, internal capsule). For all but one tract identified, age-related trajectories were curvilinear (i.e., inverted ‘U-shape’), with age-related increases during childhood and adolescence followed by decreases in middle adulthood. Identification of peaks in the trajectories suggests that age-related losses in fractional anisotropy occur as early as 23 years of age, with mean onset at 30 years of age. Our findings demonstrate that data-driven analytic techniques may be fruitfully applied to extant diffusion tensor imaging datasets in normative and neuropsychiatric samples. Public Library of Science 2011-08-31 /pmc/articles/PMC3166135/ /pubmed/21909351 http://dx.doi.org/10.1371/journal.pone.0023437 Text en Imperati et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Imperati, Davide
Colcombe, Stan
Kelly, Clare
Di Martino, Adriana
Zhou, Juan
Castellanos, F. Xavier
Milham, Michael P.
Differential Development of Human Brain White Matter Tracts
title Differential Development of Human Brain White Matter Tracts
title_full Differential Development of Human Brain White Matter Tracts
title_fullStr Differential Development of Human Brain White Matter Tracts
title_full_unstemmed Differential Development of Human Brain White Matter Tracts
title_short Differential Development of Human Brain White Matter Tracts
title_sort differential development of human brain white matter tracts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166135/
https://www.ncbi.nlm.nih.gov/pubmed/21909351
http://dx.doi.org/10.1371/journal.pone.0023437
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