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Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy

Mounting evidence suggests an association between cerebellar atrophy and cognitive impairment in the main frontotemporal dementia syndromes. In contrast, whether cerebellar atrophy is present in the motor syndromes associated with frontotemporal lobar degeneration (corticobasal syndrome and progress...

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Autores principales: Tse, Nga Yan, Chen, Yu, Irish, Muireann, Cordato, Nicholas J, Landin-Romero, Ramon, Hodges, John R, Piguet, Olivier, Ahmed, Rebekah M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753056/
https://www.ncbi.nlm.nih.gov/pubmed/33381758
http://dx.doi.org/10.1093/braincomms/fcaa194
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author Tse, Nga Yan
Chen, Yu
Irish, Muireann
Cordato, Nicholas J
Landin-Romero, Ramon
Hodges, John R
Piguet, Olivier
Ahmed, Rebekah M
author_facet Tse, Nga Yan
Chen, Yu
Irish, Muireann
Cordato, Nicholas J
Landin-Romero, Ramon
Hodges, John R
Piguet, Olivier
Ahmed, Rebekah M
author_sort Tse, Nga Yan
collection PubMed
description Mounting evidence suggests an association between cerebellar atrophy and cognitive impairment in the main frontotemporal dementia syndromes. In contrast, whether cerebellar atrophy is present in the motor syndromes associated with frontotemporal lobar degeneration (corticobasal syndrome and progressive supranuclear palsy) and the extent of its contribution to their cognitive profile remain poorly understood. The current study aimed to comprehensively chart profiles of cognitive impairment in relation to cerebellar atrophy in 49 dementia patients (corticobasal syndrome = 33; progressive supranuclear palsy = 16) compared to 33 age-, sex- and education-matched healthy controls. Relative to controls, corticobasal syndrome and progressive supranuclear palsy patients demonstrated characteristic cognitive impairment, spanning the majority of cognitive domains including attention and processing speed, language, working memory, and executive function with relative preservation of verbal and nonverbal memory. Voxel-based morphometry analysis revealed largely overlapping patterns of cerebellar atrophy in corticobasal syndrome and progressive supranuclear palsy relative to controls, primarily involving bilateral Crus II extending into adjacent lobules VIIb and VIIIa. After controlling for overall cerebral atrophy and disease duration, exploratory voxel-wise general linear model analysis revealed distinct cerebellar subregions differentially implicated across cognitive domains in each patient group. In corticobasal syndrome, reduction in grey matter intensity in the left Crus I was significantly correlated with executive dysfunction. In progressive supranuclear palsy, integrity of the vermis and adjacent right lobules I–IV was significantly associated with language performance. These results are consistent with the well-established role of Crus I in executive functions and provide further supporting evidence for vermal involvement in cognitive processing. The current study presents the first detailed exploration of the role of cerebellar atrophy in cognitive deficits in corticobasal syndrome and progressive supranuclear palsy, offering insights into the cerebellum’s contribution to cognitive processing even in neurodegenerative syndromes characterized by motor impairment.
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spelling pubmed-77530562020-12-29 Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy Tse, Nga Yan Chen, Yu Irish, Muireann Cordato, Nicholas J Landin-Romero, Ramon Hodges, John R Piguet, Olivier Ahmed, Rebekah M Brain Commun Original Article Mounting evidence suggests an association between cerebellar atrophy and cognitive impairment in the main frontotemporal dementia syndromes. In contrast, whether cerebellar atrophy is present in the motor syndromes associated with frontotemporal lobar degeneration (corticobasal syndrome and progressive supranuclear palsy) and the extent of its contribution to their cognitive profile remain poorly understood. The current study aimed to comprehensively chart profiles of cognitive impairment in relation to cerebellar atrophy in 49 dementia patients (corticobasal syndrome = 33; progressive supranuclear palsy = 16) compared to 33 age-, sex- and education-matched healthy controls. Relative to controls, corticobasal syndrome and progressive supranuclear palsy patients demonstrated characteristic cognitive impairment, spanning the majority of cognitive domains including attention and processing speed, language, working memory, and executive function with relative preservation of verbal and nonverbal memory. Voxel-based morphometry analysis revealed largely overlapping patterns of cerebellar atrophy in corticobasal syndrome and progressive supranuclear palsy relative to controls, primarily involving bilateral Crus II extending into adjacent lobules VIIb and VIIIa. After controlling for overall cerebral atrophy and disease duration, exploratory voxel-wise general linear model analysis revealed distinct cerebellar subregions differentially implicated across cognitive domains in each patient group. In corticobasal syndrome, reduction in grey matter intensity in the left Crus I was significantly correlated with executive dysfunction. In progressive supranuclear palsy, integrity of the vermis and adjacent right lobules I–IV was significantly associated with language performance. These results are consistent with the well-established role of Crus I in executive functions and provide further supporting evidence for vermal involvement in cognitive processing. The current study presents the first detailed exploration of the role of cerebellar atrophy in cognitive deficits in corticobasal syndrome and progressive supranuclear palsy, offering insights into the cerebellum’s contribution to cognitive processing even in neurodegenerative syndromes characterized by motor impairment. Oxford University Press 2020-11-16 /pmc/articles/PMC7753056/ /pubmed/33381758 http://dx.doi.org/10.1093/braincomms/fcaa194 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Tse, Nga Yan
Chen, Yu
Irish, Muireann
Cordato, Nicholas J
Landin-Romero, Ramon
Hodges, John R
Piguet, Olivier
Ahmed, Rebekah M
Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title_full Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title_fullStr Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title_full_unstemmed Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title_short Cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
title_sort cerebellar contributions to cognition in corticobasal syndrome and progressive supranuclear palsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753056/
https://www.ncbi.nlm.nih.gov/pubmed/33381758
http://dx.doi.org/10.1093/braincomms/fcaa194
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