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Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment
Objectives: To reveal the neural basis of Wernicke's encephalopathy (WE) with impaired vestibulo-ocular reflex (VOR), we evaluated resting-state functional connectivity (rs-fc) in the vestibular processing brain regions. Methods: Rs-fc between the vestibular regions and the rest of the brain we...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776602/ https://www.ncbi.nlm.nih.gov/pubmed/31611841 http://dx.doi.org/10.3389/fneur.2019.01035 |
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author | Oh, Sun-Young Lee, Juhyung Kang, Jin-Ju Park, Yeong-Hun Kim, Ko Woon Lee, Jong-Min Kim, Ji-Soo Dieterich, Marianne |
author_facet | Oh, Sun-Young Lee, Juhyung Kang, Jin-Ju Park, Yeong-Hun Kim, Ko Woon Lee, Jong-Min Kim, Ji-Soo Dieterich, Marianne |
author_sort | Oh, Sun-Young |
collection | PubMed |
description | Objectives: To reveal the neural basis of Wernicke's encephalopathy (WE) with impaired vestibulo-ocular reflex (VOR), we evaluated resting-state functional connectivity (rs-fc) in the vestibular processing brain regions. Methods: Rs-fc between the vestibular regions and the rest of the brain were compared with neurotological features including the head-impulse tests (vHIT) and caloric responses in patients with WE (n = 5, mean age 53.4 ± 10 years) and healthy controls (n = 20, mean age 55.0 ± 9.2 years). Rs-fc analyses employed a region of interest (ROI)-based approach using regions selected a priori that participate in vestibular processing including the cerebellar vermis, insula, parietal operculum, and calcarine cortex. Results: The main neurologic findings for patients with WE were mental changes; gait ataxia; spontaneous and gaze-evoked nystagmus (GEN); and bilaterally positive HIT for the horizontal canals. Video HIT documented bilateral horizontal canal dysfunction with decreased gain and corrective saccades. Caloric irrigation and rotation chair testing revealed prominent bilateral horizontal canal paresis. Patients with WE also had decreased spatial memory, which substantially recovered after treatments. Functional connections at the predefined seed regions, including the insular cortex and parietal operculum, were attenuated in the WE group compared to healthy controls. Conclusions: WE is related to impaired VOR and visuospatial dysfunction, and fMRI documented changes in the rs-fc of multisensory vestibular processing regions including the insula, parietal operculum, and superior temporal gyrus, which participate in integration of vestibular perception. |
format | Online Article Text |
id | pubmed-6776602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67766022019-10-14 Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment Oh, Sun-Young Lee, Juhyung Kang, Jin-Ju Park, Yeong-Hun Kim, Ko Woon Lee, Jong-Min Kim, Ji-Soo Dieterich, Marianne Front Neurol Neurology Objectives: To reveal the neural basis of Wernicke's encephalopathy (WE) with impaired vestibulo-ocular reflex (VOR), we evaluated resting-state functional connectivity (rs-fc) in the vestibular processing brain regions. Methods: Rs-fc between the vestibular regions and the rest of the brain were compared with neurotological features including the head-impulse tests (vHIT) and caloric responses in patients with WE (n = 5, mean age 53.4 ± 10 years) and healthy controls (n = 20, mean age 55.0 ± 9.2 years). Rs-fc analyses employed a region of interest (ROI)-based approach using regions selected a priori that participate in vestibular processing including the cerebellar vermis, insula, parietal operculum, and calcarine cortex. Results: The main neurologic findings for patients with WE were mental changes; gait ataxia; spontaneous and gaze-evoked nystagmus (GEN); and bilaterally positive HIT for the horizontal canals. Video HIT documented bilateral horizontal canal dysfunction with decreased gain and corrective saccades. Caloric irrigation and rotation chair testing revealed prominent bilateral horizontal canal paresis. Patients with WE also had decreased spatial memory, which substantially recovered after treatments. Functional connections at the predefined seed regions, including the insular cortex and parietal operculum, were attenuated in the WE group compared to healthy controls. Conclusions: WE is related to impaired VOR and visuospatial dysfunction, and fMRI documented changes in the rs-fc of multisensory vestibular processing regions including the insula, parietal operculum, and superior temporal gyrus, which participate in integration of vestibular perception. Frontiers Media S.A. 2019-09-27 /pmc/articles/PMC6776602/ /pubmed/31611841 http://dx.doi.org/10.3389/fneur.2019.01035 Text en Copyright © 2019 Oh, Lee, Kang, Park, Kim, Lee, Kim and Dieterich. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Oh, Sun-Young Lee, Juhyung Kang, Jin-Ju Park, Yeong-Hun Kim, Ko Woon Lee, Jong-Min Kim, Ji-Soo Dieterich, Marianne Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title | Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title_full | Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title_fullStr | Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title_full_unstemmed | Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title_short | Altered Resting-State Functional Connectivity in Wernicke's Encephalopathy With Vestibular Impairment |
title_sort | altered resting-state functional connectivity in wernicke's encephalopathy with vestibular impairment |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776602/ https://www.ncbi.nlm.nih.gov/pubmed/31611841 http://dx.doi.org/10.3389/fneur.2019.01035 |
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