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Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis

BACKGROUND: A bidirectional functional link between vestibular and fear-related disorders has been previously suggested. OBJECTIVE: To test a potential overlap of vestibular and fear systems with regard to their brain imaging representation maps. METHODS: By use of voxel-based mapping permutation of...

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Autores principales: Neumann, Nicola, Fullana, Miquel A., Radua, Joaquim, Brandt, Thomas, Dieterich, Marianne, Lotze, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025232/
https://www.ncbi.nlm.nih.gov/pubmed/36723684
http://dx.doi.org/10.1007/s00415-023-11568-7
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author Neumann, Nicola
Fullana, Miquel A.
Radua, Joaquim
Brandt, Thomas
Dieterich, Marianne
Lotze, Martin
author_facet Neumann, Nicola
Fullana, Miquel A.
Radua, Joaquim
Brandt, Thomas
Dieterich, Marianne
Lotze, Martin
author_sort Neumann, Nicola
collection PubMed
description BACKGROUND: A bidirectional functional link between vestibular and fear-related disorders has been previously suggested. OBJECTIVE: To test a potential overlap of vestibular and fear systems with regard to their brain imaging representation maps. METHODS: By use of voxel-based mapping permutation of subject images, we conducted a meta-analysis of earlier functional magnetic resonance imaging (fMRI) studies applying vestibular stimulation and fear conditioning in healthy volunteers. RESULTS: Common clusters of concordance of vestibular stimulation and fear conditioning were found in the bilateral anterior insula cortex, ventrolateral prefrontal cortex and the right temporal pole, bilaterally in the adjacent ventrolateral prefrontal cortex, cingulate gyrus, secondary somatosensory cortex, superior temporal and intraparietal lobe, supplementary motor area and premotor cortex, as well as subcortical areas, such as the bilateral thalamus, mesencephalic brainstem including the collicular complex, pons, cerebellar vermis and bilateral cerebellar hemispheres. Peak areas of high concordance for activations during vestibular stimulation but deactivations during fear conditioning were centered on the posterior insula and S2. CONCLUSIONS: The structural overlap of both networks allows the following functional interpretations: first, the amygdala, superior colliculi, and antero-medial thalamus might represent a release of preprogramed sensorimotor patterns of approach or avoidance. Second, the activation (vestibular system) and deactivation (fear system) of the bilateral posterior insula is compatible with the view that downregulation of the fear network by acute vestibular disorders or unfamiliar vestibular stimulation makes unpleasant perceived body accelerations less distressing. This also fits the clinical observation that patients with bilateral vestibular loss suffer from less vertigo-related anxiety. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11568-7.
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spelling pubmed-100252322023-03-21 Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis Neumann, Nicola Fullana, Miquel A. Radua, Joaquim Brandt, Thomas Dieterich, Marianne Lotze, Martin J Neurol Original Communication BACKGROUND: A bidirectional functional link between vestibular and fear-related disorders has been previously suggested. OBJECTIVE: To test a potential overlap of vestibular and fear systems with regard to their brain imaging representation maps. METHODS: By use of voxel-based mapping permutation of subject images, we conducted a meta-analysis of earlier functional magnetic resonance imaging (fMRI) studies applying vestibular stimulation and fear conditioning in healthy volunteers. RESULTS: Common clusters of concordance of vestibular stimulation and fear conditioning were found in the bilateral anterior insula cortex, ventrolateral prefrontal cortex and the right temporal pole, bilaterally in the adjacent ventrolateral prefrontal cortex, cingulate gyrus, secondary somatosensory cortex, superior temporal and intraparietal lobe, supplementary motor area and premotor cortex, as well as subcortical areas, such as the bilateral thalamus, mesencephalic brainstem including the collicular complex, pons, cerebellar vermis and bilateral cerebellar hemispheres. Peak areas of high concordance for activations during vestibular stimulation but deactivations during fear conditioning were centered on the posterior insula and S2. CONCLUSIONS: The structural overlap of both networks allows the following functional interpretations: first, the amygdala, superior colliculi, and antero-medial thalamus might represent a release of preprogramed sensorimotor patterns of approach or avoidance. Second, the activation (vestibular system) and deactivation (fear system) of the bilateral posterior insula is compatible with the view that downregulation of the fear network by acute vestibular disorders or unfamiliar vestibular stimulation makes unpleasant perceived body accelerations less distressing. This also fits the clinical observation that patients with bilateral vestibular loss suffer from less vertigo-related anxiety. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11568-7. Springer Berlin Heidelberg 2023-02-01 2023 /pmc/articles/PMC10025232/ /pubmed/36723684 http://dx.doi.org/10.1007/s00415-023-11568-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Neumann, Nicola
Fullana, Miquel A.
Radua, Joaquim
Brandt, Thomas
Dieterich, Marianne
Lotze, Martin
Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title_full Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title_fullStr Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title_full_unstemmed Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title_short Common neural correlates of vestibular stimulation and fear learning: an fMRI meta-analysis
title_sort common neural correlates of vestibular stimulation and fear learning: an fmri meta-analysis
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025232/
https://www.ncbi.nlm.nih.gov/pubmed/36723684
http://dx.doi.org/10.1007/s00415-023-11568-7
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