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The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease

Area OP2 in the posterior peri-sylvian cortex has been proposed to be the core human vestibular cortex. We investigated the functional anatomy of OP2 and adjacent areas (OP2(+)) using spatially constrained independent component analysis (ICA) of functional magnetic resonance imaging (fMRI) data from...

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Autores principales: Ibitoye, Richard T, Mallas, Emma-Jane, Bourke, Niall J, Kaski, Diego, Bronstein, Adolfo M, Sharp, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890474/
https://www.ncbi.nlm.nih.gov/pubmed/35235642
http://dx.doi.org/10.1093/cercor/bhac085
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author Ibitoye, Richard T
Mallas, Emma-Jane
Bourke, Niall J
Kaski, Diego
Bronstein, Adolfo M
Sharp, David J
author_facet Ibitoye, Richard T
Mallas, Emma-Jane
Bourke, Niall J
Kaski, Diego
Bronstein, Adolfo M
Sharp, David J
author_sort Ibitoye, Richard T
collection PubMed
description Area OP2 in the posterior peri-sylvian cortex has been proposed to be the core human vestibular cortex. We investigated the functional anatomy of OP2 and adjacent areas (OP2(+)) using spatially constrained independent component analysis (ICA) of functional magnetic resonance imaging (fMRI) data from the Human Connectome Project. Ten ICA-derived subregions were identified. OP2(+) responses to vestibular and visual motion were analyzed in 17 controls and 17 right-sided vestibular neuritis patients who had previously undergone caloric and optokinetic stimulation during fMRI. In controls, a posterior part of right OP2(+) showed: (i) direction-selective responses to visual motion and (ii) activation during caloric stimulation that correlated positively with perceived self-motion, and negatively with visual dependence and peak slow-phase nystagmus velocity. Patients showed abnormal OP2(+) activity, with an absence of visual or caloric activation of the healthy ear and no correlations with vertigo or visual dependence—despite normal slow-phase nystagmus responses to caloric stimulation. Activity in a lateral part of right OP2(+) correlated with chronic visually induced dizziness in patients. In summary, distinct functional subregions of right OP2(+) show strong connectivity to other vestibular areas and a profile of caloric and visual responses, suggesting a central role for vestibular function in health and disease.
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spelling pubmed-98904742023-02-02 The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease Ibitoye, Richard T Mallas, Emma-Jane Bourke, Niall J Kaski, Diego Bronstein, Adolfo M Sharp, David J Cereb Cortex Original Article Area OP2 in the posterior peri-sylvian cortex has been proposed to be the core human vestibular cortex. We investigated the functional anatomy of OP2 and adjacent areas (OP2(+)) using spatially constrained independent component analysis (ICA) of functional magnetic resonance imaging (fMRI) data from the Human Connectome Project. Ten ICA-derived subregions were identified. OP2(+) responses to vestibular and visual motion were analyzed in 17 controls and 17 right-sided vestibular neuritis patients who had previously undergone caloric and optokinetic stimulation during fMRI. In controls, a posterior part of right OP2(+) showed: (i) direction-selective responses to visual motion and (ii) activation during caloric stimulation that correlated positively with perceived self-motion, and negatively with visual dependence and peak slow-phase nystagmus velocity. Patients showed abnormal OP2(+) activity, with an absence of visual or caloric activation of the healthy ear and no correlations with vertigo or visual dependence—despite normal slow-phase nystagmus responses to caloric stimulation. Activity in a lateral part of right OP2(+) correlated with chronic visually induced dizziness in patients. In summary, distinct functional subregions of right OP2(+) show strong connectivity to other vestibular areas and a profile of caloric and visual responses, suggesting a central role for vestibular function in health and disease. Oxford University Press 2022-03-02 /pmc/articles/PMC9890474/ /pubmed/35235642 http://dx.doi.org/10.1093/cercor/bhac085 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ibitoye, Richard T
Mallas, Emma-Jane
Bourke, Niall J
Kaski, Diego
Bronstein, Adolfo M
Sharp, David J
The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title_full The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title_fullStr The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title_full_unstemmed The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title_short The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease
title_sort human vestibular cortex: functional anatomy of op2, its connectivity and the effect of vestibular disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890474/
https://www.ncbi.nlm.nih.gov/pubmed/35235642
http://dx.doi.org/10.1093/cercor/bhac085
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