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White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems

There is an increasing awareness of the involvement of thalamic connectivity on higher level cortical functioning in the human brain. This is reflected by the influence of thalamic stimulation on cortical activity and behavior as well as apparently cortical lesion syndromes occurring as a function o...

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Autores principales: O'Muircheartaigh, Jonathan, Keller, Simon S., Barker, Gareth J., Richardson, Mark P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816794/
https://www.ncbi.nlm.nih.gov/pubmed/25899706
http://dx.doi.org/10.1093/cercor/bhv063
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author O'Muircheartaigh, Jonathan
Keller, Simon S.
Barker, Gareth J.
Richardson, Mark P.
author_facet O'Muircheartaigh, Jonathan
Keller, Simon S.
Barker, Gareth J.
Richardson, Mark P.
author_sort O'Muircheartaigh, Jonathan
collection PubMed
description There is an increasing awareness of the involvement of thalamic connectivity on higher level cortical functioning in the human brain. This is reflected by the influence of thalamic stimulation on cortical activity and behavior as well as apparently cortical lesion syndromes occurring as a function of small thalamic insults. Here, we attempt to noninvasively test the correspondence of structural and functional connectivity of the human thalamus using diffusion-weighted and resting-state functional MRI. Using a large sample of 102 adults, we apply tensor independent component analysis to diffusion MRI tractography data to blindly parcellate bilateral thalamus according to diffusion tractography-defined structural connectivity. Using resting-state functional MRI collected in the same subjects, we show that the resulting structurally defined thalamic regions map to spatially distinct, and anatomically predictable, whole-brain functional networks in the same subjects. Although there was significant variability in the functional connectivity patterns, the resulting 51 structural and functional patterns could broadly be reduced to a subset of 7 similar core network types. These networks were distinct from typical cortical resting-state networks. Importantly, these networks were distributed across the brain and, in a subset, map extremely well to known thalamocortico-basal-ganglial loops.
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spelling pubmed-48167942016-04-04 White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems O'Muircheartaigh, Jonathan Keller, Simon S. Barker, Gareth J. Richardson, Mark P. Cereb Cortex Articles There is an increasing awareness of the involvement of thalamic connectivity on higher level cortical functioning in the human brain. This is reflected by the influence of thalamic stimulation on cortical activity and behavior as well as apparently cortical lesion syndromes occurring as a function of small thalamic insults. Here, we attempt to noninvasively test the correspondence of structural and functional connectivity of the human thalamus using diffusion-weighted and resting-state functional MRI. Using a large sample of 102 adults, we apply tensor independent component analysis to diffusion MRI tractography data to blindly parcellate bilateral thalamus according to diffusion tractography-defined structural connectivity. Using resting-state functional MRI collected in the same subjects, we show that the resulting structurally defined thalamic regions map to spatially distinct, and anatomically predictable, whole-brain functional networks in the same subjects. Although there was significant variability in the functional connectivity patterns, the resulting 51 structural and functional patterns could broadly be reduced to a subset of 7 similar core network types. These networks were distinct from typical cortical resting-state networks. Importantly, these networks were distributed across the brain and, in a subset, map extremely well to known thalamocortico-basal-ganglial loops. Oxford University Press 2015-11 2015-04-21 /pmc/articles/PMC4816794/ /pubmed/25899706 http://dx.doi.org/10.1093/cercor/bhv063 Text en © The Author 2015. Published by Oxford University Press http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
O'Muircheartaigh, Jonathan
Keller, Simon S.
Barker, Gareth J.
Richardson, Mark P.
White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title_full White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title_fullStr White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title_full_unstemmed White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title_short White Matter Connectivity of the Thalamus Delineates the Functional Architecture of Competing Thalamocortical Systems
title_sort white matter connectivity of the thalamus delineates the functional architecture of competing thalamocortical systems
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816794/
https://www.ncbi.nlm.nih.gov/pubmed/25899706
http://dx.doi.org/10.1093/cercor/bhv063
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