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Altered white matter connectivity associated with visual hallucinations following occipital stroke
INTRODUCTION: Visual hallucinations that arise following vision loss stem from aberrant functional activity in visual cortices and an imbalance of activity across associated cortical and subcortical networks subsequent to visual pathway damage. We sought to determine if structural changes in white m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991596/ https://www.ncbi.nlm.nih.gov/pubmed/29781583 http://dx.doi.org/10.1002/brb3.1010 |
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author | Rafique, Sara A. Richards, John R. Steeves, Jennifer K. E. |
author_facet | Rafique, Sara A. Richards, John R. Steeves, Jennifer K. E. |
author_sort | Rafique, Sara A. |
collection | PubMed |
description | INTRODUCTION: Visual hallucinations that arise following vision loss stem from aberrant functional activity in visual cortices and an imbalance of activity across associated cortical and subcortical networks subsequent to visual pathway damage. We sought to determine if structural changes in white matter connectivity play a role in cases of chronic visual hallucinations associated with visual cortical damage. METHODS: We performed diffusion tensor imaging (DTI) and probabilistic fiber tractography to assess white matter connectivity in a patient suffering from continuous and disruptive phosphene (simple) visual hallucinations for more than 2 years following right occipital stroke. We compared these data to that of healthy age‐matched controls. RESULTS: Probabilistic tractography to reconstruct white matter tracts suggests regeneration of terminal fibers of the ipsilesional optic radiations in the patient. However, arrangement of the converse reconstruction of these tracts, which were seeded from the ipsilesional visual cortex to the intrahemispheric lateral geniculate body, remained disrupted. We further observed compromised structural characteristics, and changes in diffusion (measured using diffusion tensor indices) of white matter tracts in the patient connecting the visual cortex with frontal and temporal regions, and also in interhemispheric connectivity between visual cortices. CONCLUSIONS: Cortical remapping and the disruption of communication between visual cortices and remote regions are consistent with our previous functional magnetic resonance imaging (fMRI) data showing imbalanced functional activity of the same regions in this patient (Rafique et al, 2016, Neurology, 87, 1493–1500). Long‐term adaptive and disruptive changes in white matter connectivity may account for the rare nature of cases presenting with chronic and continuous visual hallucinations. |
format | Online Article Text |
id | pubmed-5991596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59915962018-06-20 Altered white matter connectivity associated with visual hallucinations following occipital stroke Rafique, Sara A. Richards, John R. Steeves, Jennifer K. E. Brain Behav Original Research INTRODUCTION: Visual hallucinations that arise following vision loss stem from aberrant functional activity in visual cortices and an imbalance of activity across associated cortical and subcortical networks subsequent to visual pathway damage. We sought to determine if structural changes in white matter connectivity play a role in cases of chronic visual hallucinations associated with visual cortical damage. METHODS: We performed diffusion tensor imaging (DTI) and probabilistic fiber tractography to assess white matter connectivity in a patient suffering from continuous and disruptive phosphene (simple) visual hallucinations for more than 2 years following right occipital stroke. We compared these data to that of healthy age‐matched controls. RESULTS: Probabilistic tractography to reconstruct white matter tracts suggests regeneration of terminal fibers of the ipsilesional optic radiations in the patient. However, arrangement of the converse reconstruction of these tracts, which were seeded from the ipsilesional visual cortex to the intrahemispheric lateral geniculate body, remained disrupted. We further observed compromised structural characteristics, and changes in diffusion (measured using diffusion tensor indices) of white matter tracts in the patient connecting the visual cortex with frontal and temporal regions, and also in interhemispheric connectivity between visual cortices. CONCLUSIONS: Cortical remapping and the disruption of communication between visual cortices and remote regions are consistent with our previous functional magnetic resonance imaging (fMRI) data showing imbalanced functional activity of the same regions in this patient (Rafique et al, 2016, Neurology, 87, 1493–1500). Long‐term adaptive and disruptive changes in white matter connectivity may account for the rare nature of cases presenting with chronic and continuous visual hallucinations. John Wiley and Sons Inc. 2018-05-21 /pmc/articles/PMC5991596/ /pubmed/29781583 http://dx.doi.org/10.1002/brb3.1010 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://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 Research Rafique, Sara A. Richards, John R. Steeves, Jennifer K. E. Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title | Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title_full | Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title_fullStr | Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title_full_unstemmed | Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title_short | Altered white matter connectivity associated with visual hallucinations following occipital stroke |
title_sort | altered white matter connectivity associated with visual hallucinations following occipital stroke |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991596/ https://www.ncbi.nlm.nih.gov/pubmed/29781583 http://dx.doi.org/10.1002/brb3.1010 |
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