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Parcellation‐based tractographic modeling of the salience network through meta‐analysis

BACKGROUND: The salience network (SN) is a transitory mediator between active and passive states of mind. Multiple cortical areas, including the opercular, insular, and cingulate cortices have been linked in this processing, though knowledge of network connectivity has been devoid of structural spec...

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Autores principales: Briggs, Robert G., Young, Isabella M., Dadario, Nicholas B., Fonseka, R. Dineth, Hormovas, Jorge, Allan, Parker, Larsen, Micah L., Lin, Yueh‐Hsin, Tanglay, Onur, Maxwell, B. David, Conner, Andrew K., Stafford, Jordan F., Glenn, Chad A., Teo, Charles, Sughrue, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304834/
https://www.ncbi.nlm.nih.gov/pubmed/35733239
http://dx.doi.org/10.1002/brb3.2646
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author Briggs, Robert G.
Young, Isabella M.
Dadario, Nicholas B.
Fonseka, R. Dineth
Hormovas, Jorge
Allan, Parker
Larsen, Micah L.
Lin, Yueh‐Hsin
Tanglay, Onur
Maxwell, B. David
Conner, Andrew K.
Stafford, Jordan F.
Glenn, Chad A.
Teo, Charles
Sughrue, Michael E.
author_facet Briggs, Robert G.
Young, Isabella M.
Dadario, Nicholas B.
Fonseka, R. Dineth
Hormovas, Jorge
Allan, Parker
Larsen, Micah L.
Lin, Yueh‐Hsin
Tanglay, Onur
Maxwell, B. David
Conner, Andrew K.
Stafford, Jordan F.
Glenn, Chad A.
Teo, Charles
Sughrue, Michael E.
author_sort Briggs, Robert G.
collection PubMed
description BACKGROUND: The salience network (SN) is a transitory mediator between active and passive states of mind. Multiple cortical areas, including the opercular, insular, and cingulate cortices have been linked in this processing, though knowledge of network connectivity has been devoid of structural specificity. OBJECTIVE: The current study sought to create an anatomically specific connectivity model of the neural substrates involved in the salience network. METHODS: A literature search of PubMed and BrainMap Sleuth was conducted for resting‐state and task‐based fMRI studies relevant to the salience network according to PRISMA guidelines. Publicly available meta‐analytic software was utilized to extract relevant fMRI data for the creation of an activation likelihood estimation (ALE) map and relevant parcellations from the human connectome project overlapping with the ALE data were identified for inclusion in our SN model. DSI‐based fiber tractography was then performed on publicaly available data from healthy subjects to determine the structural connections between cortical parcellations comprising the network. RESULTS: Nine cortical regions were found to comprise the salience network: areas AVI (anterior ventral insula), MI (middle insula), FOP4 (frontal operculum 4), FOP5 (frontal operculum 5), a24pr (anterior 24 prime), a32pr (anterior 32 prime), p32pr (posterior 32 prime), and SCEF (supplementary and cingulate eye field), and 46. The frontal aslant tract was found to connect the opercular‐insular cluster to the middle cingulate clusters of the network, while mostly short U‐fibers connected adjacent nodes of the network. CONCLUSION: Here we provide an anatomically specific connectivity model of the neural substrates involved in the salience network. These results may serve as an empiric basis for clinical translation in this region and for future study which seeks to expand our understanding of how specific neural substrates are involved in salience processing and guide subsequent human behavior.
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spelling pubmed-93048342022-07-26 Parcellation‐based tractographic modeling of the salience network through meta‐analysis Briggs, Robert G. Young, Isabella M. Dadario, Nicholas B. Fonseka, R. Dineth Hormovas, Jorge Allan, Parker Larsen, Micah L. Lin, Yueh‐Hsin Tanglay, Onur Maxwell, B. David Conner, Andrew K. Stafford, Jordan F. Glenn, Chad A. Teo, Charles Sughrue, Michael E. Brain Behav Original Articles BACKGROUND: The salience network (SN) is a transitory mediator between active and passive states of mind. Multiple cortical areas, including the opercular, insular, and cingulate cortices have been linked in this processing, though knowledge of network connectivity has been devoid of structural specificity. OBJECTIVE: The current study sought to create an anatomically specific connectivity model of the neural substrates involved in the salience network. METHODS: A literature search of PubMed and BrainMap Sleuth was conducted for resting‐state and task‐based fMRI studies relevant to the salience network according to PRISMA guidelines. Publicly available meta‐analytic software was utilized to extract relevant fMRI data for the creation of an activation likelihood estimation (ALE) map and relevant parcellations from the human connectome project overlapping with the ALE data were identified for inclusion in our SN model. DSI‐based fiber tractography was then performed on publicaly available data from healthy subjects to determine the structural connections between cortical parcellations comprising the network. RESULTS: Nine cortical regions were found to comprise the salience network: areas AVI (anterior ventral insula), MI (middle insula), FOP4 (frontal operculum 4), FOP5 (frontal operculum 5), a24pr (anterior 24 prime), a32pr (anterior 32 prime), p32pr (posterior 32 prime), and SCEF (supplementary and cingulate eye field), and 46. The frontal aslant tract was found to connect the opercular‐insular cluster to the middle cingulate clusters of the network, while mostly short U‐fibers connected adjacent nodes of the network. CONCLUSION: Here we provide an anatomically specific connectivity model of the neural substrates involved in the salience network. These results may serve as an empiric basis for clinical translation in this region and for future study which seeks to expand our understanding of how specific neural substrates are involved in salience processing and guide subsequent human behavior. John Wiley and Sons Inc. 2022-06-22 /pmc/articles/PMC9304834/ /pubmed/35733239 http://dx.doi.org/10.1002/brb3.2646 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Briggs, Robert G.
Young, Isabella M.
Dadario, Nicholas B.
Fonseka, R. Dineth
Hormovas, Jorge
Allan, Parker
Larsen, Micah L.
Lin, Yueh‐Hsin
Tanglay, Onur
Maxwell, B. David
Conner, Andrew K.
Stafford, Jordan F.
Glenn, Chad A.
Teo, Charles
Sughrue, Michael E.
Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title_full Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title_fullStr Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title_full_unstemmed Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title_short Parcellation‐based tractographic modeling of the salience network through meta‐analysis
title_sort parcellation‐based tractographic modeling of the salience network through meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304834/
https://www.ncbi.nlm.nih.gov/pubmed/35733239
http://dx.doi.org/10.1002/brb3.2646
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