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Apraxia in progressive nonfluent aphasia

The clinical and neuroanatomical correlates of specific apraxias in neurodegenerative disease are not well understood. Here we addressed this issue in progressive nonfluent aphasia (PNFA), a canonical subtype of frontotemporal lobar degeneration that has been consistently associated with apraxia of...

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Autores principales: Rohrer, Jonathan Daniel, Rossor, Martin N., Warren, Jason D.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848723/
https://www.ncbi.nlm.nih.gov/pubmed/19908082
http://dx.doi.org/10.1007/s00415-009-5371-4
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author Rohrer, Jonathan Daniel
Rossor, Martin N.
Warren, Jason D.
author_facet Rohrer, Jonathan Daniel
Rossor, Martin N.
Warren, Jason D.
author_sort Rohrer, Jonathan Daniel
collection PubMed
description The clinical and neuroanatomical correlates of specific apraxias in neurodegenerative disease are not well understood. Here we addressed this issue in progressive nonfluent aphasia (PNFA), a canonical subtype of frontotemporal lobar degeneration that has been consistently associated with apraxia of speech (AOS) and in some cases orofacial apraxia, limb apraxia and/or parkinsonism. Sixteen patients with PNFA according to current consensus criteria were studied. Three patients had a corticobasal syndrome (CBS) and two a progressive supranuclear palsy (PSP) syndrome. Speech, orofacial and limb praxis functions were assessed using the Apraxia Battery for Adults-2 and a voxel-based morphometry (VBM) analysis was conducted on brain MRI scans from the patient cohort in order to identify neuroanatomical correlates. All patients had AOS based on reduced diadochokinetic rate, 69% of cases had an abnormal orofacial apraxia score and 44% of cases (including the three CBS cases and one case with PSP) had an abnormal limb apraxia score. Severity of orofacial apraxia (but not AOS or limb apraxia) correlated with estimated clinical disease duration. The VBM analysis identified distinct neuroanatomical bases for each form of apraxia: the severity of AOS correlated with left posterior inferior frontal lobe atrophy; orofacial apraxia with left middle frontal, premotor and supplementary motor cortical atrophy; and limb apraxia with left inferior parietal lobe atrophy. Our findings show that apraxia of various kinds can be a clinical issue in PNFA and demonstrate that specific apraxias are clinically and anatomically dissociable within this population of patients.
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spelling pubmed-28487232010-04-12 Apraxia in progressive nonfluent aphasia Rohrer, Jonathan Daniel Rossor, Martin N. Warren, Jason D. J Neurol Original Communication The clinical and neuroanatomical correlates of specific apraxias in neurodegenerative disease are not well understood. Here we addressed this issue in progressive nonfluent aphasia (PNFA), a canonical subtype of frontotemporal lobar degeneration that has been consistently associated with apraxia of speech (AOS) and in some cases orofacial apraxia, limb apraxia and/or parkinsonism. Sixteen patients with PNFA according to current consensus criteria were studied. Three patients had a corticobasal syndrome (CBS) and two a progressive supranuclear palsy (PSP) syndrome. Speech, orofacial and limb praxis functions were assessed using the Apraxia Battery for Adults-2 and a voxel-based morphometry (VBM) analysis was conducted on brain MRI scans from the patient cohort in order to identify neuroanatomical correlates. All patients had AOS based on reduced diadochokinetic rate, 69% of cases had an abnormal orofacial apraxia score and 44% of cases (including the three CBS cases and one case with PSP) had an abnormal limb apraxia score. Severity of orofacial apraxia (but not AOS or limb apraxia) correlated with estimated clinical disease duration. The VBM analysis identified distinct neuroanatomical bases for each form of apraxia: the severity of AOS correlated with left posterior inferior frontal lobe atrophy; orofacial apraxia with left middle frontal, premotor and supplementary motor cortical atrophy; and limb apraxia with left inferior parietal lobe atrophy. Our findings show that apraxia of various kinds can be a clinical issue in PNFA and demonstrate that specific apraxias are clinically and anatomically dissociable within this population of patients. Springer-Verlag 2009-11-12 2010 /pmc/articles/PMC2848723/ /pubmed/19908082 http://dx.doi.org/10.1007/s00415-009-5371-4 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Communication
Rohrer, Jonathan Daniel
Rossor, Martin N.
Warren, Jason D.
Apraxia in progressive nonfluent aphasia
title Apraxia in progressive nonfluent aphasia
title_full Apraxia in progressive nonfluent aphasia
title_fullStr Apraxia in progressive nonfluent aphasia
title_full_unstemmed Apraxia in progressive nonfluent aphasia
title_short Apraxia in progressive nonfluent aphasia
title_sort apraxia in progressive nonfluent aphasia
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848723/
https://www.ncbi.nlm.nih.gov/pubmed/19908082
http://dx.doi.org/10.1007/s00415-009-5371-4
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