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Resting-state connectivity alterations during transient global amnesia

While the pathophysiology of transient global amnesia (TGA) is not understood, due to the specific nature of the clinical deficits, transient dysfunction in the medial temporal lobe, especially in the hippocampus, is assumed; however, concomitant disturbances in other brain regions and in executive...

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Autores principales: Zidda, Francesca, Griebe, Martin, Ebert, Anne, Ruttorf, Michaela, Roßmanith, Christina, Gass, Achim, Andoh, Jamila, Nees, Frauke, Szabo, Kristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543172/
https://www.ncbi.nlm.nih.gov/pubmed/31153000
http://dx.doi.org/10.1016/j.nicl.2019.101869
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author Zidda, Francesca
Griebe, Martin
Ebert, Anne
Ruttorf, Michaela
Roßmanith, Christina
Gass, Achim
Andoh, Jamila
Nees, Frauke
Szabo, Kristina
author_facet Zidda, Francesca
Griebe, Martin
Ebert, Anne
Ruttorf, Michaela
Roßmanith, Christina
Gass, Achim
Andoh, Jamila
Nees, Frauke
Szabo, Kristina
author_sort Zidda, Francesca
collection PubMed
description While the pathophysiology of transient global amnesia (TGA) is not understood, due to the specific nature of the clinical deficits, transient dysfunction in the medial temporal lobe, especially in the hippocampus, is assumed; however, concomitant disturbances in other brain regions and in executive function have been postulated. In this study, a cohort of 16 patients was prospectively recruited from the emergency department for resting-state functional MRI (fMRI) during the acute stage of TGA, as confirmed by a standardized neuropsychological assessment. Twenty age- and sex-matched controls, as well as twenty patients with a history of TGA, were recruited for comparison. Functional data were processed using independent component analysis (ICA), allowing the complete automatic (data-driven) identification of spontaneous network dynamics. We documented a severe disturbance in anterograde episodic long-term memory in all patients. Group-based ICA of resting-state data in acute TGA patients versus that of controls and patients with a past TGA episode demonstrated reduced FC mainly of structures belonging to the executive network (EN), but also the hippocampus, confirming its pathophysiological involvement in the disorder, as well as areas belonging to the salience network and other subcortical regions. No significant differences were found when comparing connectivity in patients with a history of TGA and controls. Our findings strengthen previous empirical and theoretical accounts of hippocampal and executive dysfunction in TGA. The disruption of frontal, parietal and insular control regions, together with disruption in the hippocampus, provides a new interpretation for the pathophysiology and neuropsychological profile of this neurological disorder on a large-scale network level
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spelling pubmed-65431722019-06-04 Resting-state connectivity alterations during transient global amnesia Zidda, Francesca Griebe, Martin Ebert, Anne Ruttorf, Michaela Roßmanith, Christina Gass, Achim Andoh, Jamila Nees, Frauke Szabo, Kristina Neuroimage Clin Regular Article While the pathophysiology of transient global amnesia (TGA) is not understood, due to the specific nature of the clinical deficits, transient dysfunction in the medial temporal lobe, especially in the hippocampus, is assumed; however, concomitant disturbances in other brain regions and in executive function have been postulated. In this study, a cohort of 16 patients was prospectively recruited from the emergency department for resting-state functional MRI (fMRI) during the acute stage of TGA, as confirmed by a standardized neuropsychological assessment. Twenty age- and sex-matched controls, as well as twenty patients with a history of TGA, were recruited for comparison. Functional data were processed using independent component analysis (ICA), allowing the complete automatic (data-driven) identification of spontaneous network dynamics. We documented a severe disturbance in anterograde episodic long-term memory in all patients. Group-based ICA of resting-state data in acute TGA patients versus that of controls and patients with a past TGA episode demonstrated reduced FC mainly of structures belonging to the executive network (EN), but also the hippocampus, confirming its pathophysiological involvement in the disorder, as well as areas belonging to the salience network and other subcortical regions. No significant differences were found when comparing connectivity in patients with a history of TGA and controls. Our findings strengthen previous empirical and theoretical accounts of hippocampal and executive dysfunction in TGA. The disruption of frontal, parietal and insular control regions, together with disruption in the hippocampus, provides a new interpretation for the pathophysiology and neuropsychological profile of this neurological disorder on a large-scale network level Elsevier 2019-05-23 /pmc/articles/PMC6543172/ /pubmed/31153000 http://dx.doi.org/10.1016/j.nicl.2019.101869 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Zidda, Francesca
Griebe, Martin
Ebert, Anne
Ruttorf, Michaela
Roßmanith, Christina
Gass, Achim
Andoh, Jamila
Nees, Frauke
Szabo, Kristina
Resting-state connectivity alterations during transient global amnesia
title Resting-state connectivity alterations during transient global amnesia
title_full Resting-state connectivity alterations during transient global amnesia
title_fullStr Resting-state connectivity alterations during transient global amnesia
title_full_unstemmed Resting-state connectivity alterations during transient global amnesia
title_short Resting-state connectivity alterations during transient global amnesia
title_sort resting-state connectivity alterations during transient global amnesia
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543172/
https://www.ncbi.nlm.nih.gov/pubmed/31153000
http://dx.doi.org/10.1016/j.nicl.2019.101869
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