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Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke

Cerebellar lesions can cause motor deficits and/or the cerebellar cognitive affective syndrome (CCAS; Schmahmann's syndrome). We used voxel-based lesion-symptom mapping to test the hypothesis that the cerebellar motor syndrome results from anterior lobe damage whereas lesions in the posterolate...

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Autores principales: Stoodley, Catherine J., MacMore, Jason P., Makris, Nikos, Sherman, Janet C., Schmahmann, Jeremy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079414/
https://www.ncbi.nlm.nih.gov/pubmed/27812503
http://dx.doi.org/10.1016/j.nicl.2016.10.013
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author Stoodley, Catherine J.
MacMore, Jason P.
Makris, Nikos
Sherman, Janet C.
Schmahmann, Jeremy D.
author_facet Stoodley, Catherine J.
MacMore, Jason P.
Makris, Nikos
Sherman, Janet C.
Schmahmann, Jeremy D.
author_sort Stoodley, Catherine J.
collection PubMed
description Cerebellar lesions can cause motor deficits and/or the cerebellar cognitive affective syndrome (CCAS; Schmahmann's syndrome). We used voxel-based lesion-symptom mapping to test the hypothesis that the cerebellar motor syndrome results from anterior lobe damage whereas lesions in the posterolateral cerebellum produce the CCAS. Eighteen patients with isolated cerebellar stroke (13 males, 5 females; 20–66 years old) were evaluated using measures of ataxia and neurocognitive ability. Patients showed a wide range of motor and cognitive performance, from normal to severely impaired; individual deficits varied according to lesion location within the cerebellum. Patients with damage to cerebellar lobules III–VI had worse ataxia scores: as predicted, the cerebellar motor syndrome resulted from lesions involving the anterior cerebellum. Poorer performance on fine motor tasks was associated primarily with strokes affecting the anterior lobe extending into lobule VI, with right-handed finger tapping and peg-placement associated with damage to the right cerebellum, and left-handed finger tapping associated with left cerebellar damage. Patients with the CCAS in the absence of cerebellar motor syndrome had damage to posterior lobe regions, with lesions leading to significantly poorer scores on language (e.g. right Crus I and II extending through IX), spatial (bilateral Crus I, Crus II, and right lobule VIII), and executive function measures (lobules VII–VIII). These data reveal clinically significant functional regions underpinning movement and cognition in the cerebellum, with a broad anterior-posterior distinction. Motor and cognitive outcomes following cerebellar damage appear to reflect the disruption of different cerebro-cerebellar motor and cognitive loops.
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spelling pubmed-50794142016-11-03 Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke Stoodley, Catherine J. MacMore, Jason P. Makris, Nikos Sherman, Janet C. Schmahmann, Jeremy D. Neuroimage Clin Regular Article Cerebellar lesions can cause motor deficits and/or the cerebellar cognitive affective syndrome (CCAS; Schmahmann's syndrome). We used voxel-based lesion-symptom mapping to test the hypothesis that the cerebellar motor syndrome results from anterior lobe damage whereas lesions in the posterolateral cerebellum produce the CCAS. Eighteen patients with isolated cerebellar stroke (13 males, 5 females; 20–66 years old) were evaluated using measures of ataxia and neurocognitive ability. Patients showed a wide range of motor and cognitive performance, from normal to severely impaired; individual deficits varied according to lesion location within the cerebellum. Patients with damage to cerebellar lobules III–VI had worse ataxia scores: as predicted, the cerebellar motor syndrome resulted from lesions involving the anterior cerebellum. Poorer performance on fine motor tasks was associated primarily with strokes affecting the anterior lobe extending into lobule VI, with right-handed finger tapping and peg-placement associated with damage to the right cerebellum, and left-handed finger tapping associated with left cerebellar damage. Patients with the CCAS in the absence of cerebellar motor syndrome had damage to posterior lobe regions, with lesions leading to significantly poorer scores on language (e.g. right Crus I and II extending through IX), spatial (bilateral Crus I, Crus II, and right lobule VIII), and executive function measures (lobules VII–VIII). These data reveal clinically significant functional regions underpinning movement and cognition in the cerebellum, with a broad anterior-posterior distinction. Motor and cognitive outcomes following cerebellar damage appear to reflect the disruption of different cerebro-cerebellar motor and cognitive loops. Elsevier 2016-10-15 /pmc/articles/PMC5079414/ /pubmed/27812503 http://dx.doi.org/10.1016/j.nicl.2016.10.013 Text en © 2016 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
Stoodley, Catherine J.
MacMore, Jason P.
Makris, Nikos
Sherman, Janet C.
Schmahmann, Jeremy D.
Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title_full Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title_fullStr Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title_full_unstemmed Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title_short Location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
title_sort location of lesion determines motor vs. cognitive consequences in patients with cerebellar stroke
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079414/
https://www.ncbi.nlm.nih.gov/pubmed/27812503
http://dx.doi.org/10.1016/j.nicl.2016.10.013
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