Cargando…

The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype

The flocculus is a region of the vestibulocerebellum dedicated to the coordination of neck, head, and eye movements for optimal posture, balance, and orienting responses. Despite growing evidence of vestibular and oculomotor impairments in the aftermath of traumatic stress, little is known about the...

Descripción completa

Detalles Bibliográficos
Autores principales: Rabellino, Daniela, Thome, Janine, Densmore, Maria, Théberge, Jean, McKinnon, Margaret C., Lanius, Ruth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657293/
https://www.ncbi.nlm.nih.gov/pubmed/36121553
http://dx.doi.org/10.1007/s12311-022-01467-4
_version_ 1785137185065795584
author Rabellino, Daniela
Thome, Janine
Densmore, Maria
Théberge, Jean
McKinnon, Margaret C.
Lanius, Ruth A.
author_facet Rabellino, Daniela
Thome, Janine
Densmore, Maria
Théberge, Jean
McKinnon, Margaret C.
Lanius, Ruth A.
author_sort Rabellino, Daniela
collection PubMed
description The flocculus is a region of the vestibulocerebellum dedicated to the coordination of neck, head, and eye movements for optimal posture, balance, and orienting responses. Despite growing evidence of vestibular and oculomotor impairments in the aftermath of traumatic stress, little is known about the effects of chronic psychological trauma on vestibulocerebellar functioning. Here, we investigated alterations in functional connectivity of the flocculus at rest among individuals with post-traumatic stress disorder (PTSD) and its dissociative subtype (PTSD + DS) as compared to healthy controls. Forty-four healthy controls, 57 PTSD, and 32 PTSD + DS underwent 6-min resting-state MRI scans. Seed-based functional connectivity analyses using the right and left flocculi as seeds were performed. These analyses revealed that, as compared to controls, PTSD and PTSD + DS showed decreased resting-state functional connectivity of the left flocculus with cortical regions involved in bodily self-consciousness, including the temporo-parietal junction, the supramarginal and angular gyri, and the superior parietal lobule. Moreover, as compared to controls, the PTSD + DS group showed decreased functional connectivity of the left flocculus with the medial prefrontal cortex, the precuneus, and the mid/posterior cingulum, key regions of the default mode network. Critically, when comparing PTSD + DS to PTSD, we observed increased functional connectivity of the right flocculus with the right anterior hippocampus, a region affected frequently by early life trauma. Taken together, our findings point toward the crucial role of the flocculus in the neurocircuitry underlying a coherent and embodied self, which can be compromised in PTSD and PTSD + DS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12311-022-01467-4.
format Online
Article
Text
id pubmed-10657293
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-106572932022-09-19 The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype Rabellino, Daniela Thome, Janine Densmore, Maria Théberge, Jean McKinnon, Margaret C. Lanius, Ruth A. Cerebellum Original Article The flocculus is a region of the vestibulocerebellum dedicated to the coordination of neck, head, and eye movements for optimal posture, balance, and orienting responses. Despite growing evidence of vestibular and oculomotor impairments in the aftermath of traumatic stress, little is known about the effects of chronic psychological trauma on vestibulocerebellar functioning. Here, we investigated alterations in functional connectivity of the flocculus at rest among individuals with post-traumatic stress disorder (PTSD) and its dissociative subtype (PTSD + DS) as compared to healthy controls. Forty-four healthy controls, 57 PTSD, and 32 PTSD + DS underwent 6-min resting-state MRI scans. Seed-based functional connectivity analyses using the right and left flocculi as seeds were performed. These analyses revealed that, as compared to controls, PTSD and PTSD + DS showed decreased resting-state functional connectivity of the left flocculus with cortical regions involved in bodily self-consciousness, including the temporo-parietal junction, the supramarginal and angular gyri, and the superior parietal lobule. Moreover, as compared to controls, the PTSD + DS group showed decreased functional connectivity of the left flocculus with the medial prefrontal cortex, the precuneus, and the mid/posterior cingulum, key regions of the default mode network. Critically, when comparing PTSD + DS to PTSD, we observed increased functional connectivity of the right flocculus with the right anterior hippocampus, a region affected frequently by early life trauma. Taken together, our findings point toward the crucial role of the flocculus in the neurocircuitry underlying a coherent and embodied self, which can be compromised in PTSD and PTSD + DS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12311-022-01467-4. Springer US 2022-09-19 2023 /pmc/articles/PMC10657293/ /pubmed/36121553 http://dx.doi.org/10.1007/s12311-022-01467-4 Text en © The Author(s) 2022 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 Article
Rabellino, Daniela
Thome, Janine
Densmore, Maria
Théberge, Jean
McKinnon, Margaret C.
Lanius, Ruth A.
The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title_full The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title_fullStr The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title_full_unstemmed The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title_short The Vestibulocerebellum and the Shattered Self: a Resting-State Functional Connectivity Study in Posttraumatic Stress Disorder and Its Dissociative Subtype
title_sort vestibulocerebellum and the shattered self: a resting-state functional connectivity study in posttraumatic stress disorder and its dissociative subtype
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657293/
https://www.ncbi.nlm.nih.gov/pubmed/36121553
http://dx.doi.org/10.1007/s12311-022-01467-4
work_keys_str_mv AT rabellinodaniela thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT thomejanine thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT densmoremaria thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT thebergejean thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT mckinnonmargaretc thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT laniusrutha thevestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT rabellinodaniela vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT thomejanine vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT densmoremaria vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT thebergejean vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT mckinnonmargaretc vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype
AT laniusrutha vestibulocerebellumandtheshatteredselfarestingstatefunctionalconnectivitystudyinposttraumaticstressdisorderanditsdissociativesubtype