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White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia

Objective: To relate fractional anisotropy (FA) changes associated with the semantic and logopenic variants of primary progressive aphasia (PPA) to measures of lexical retrieval. Methods: We collected neuropsychological testing, volumetric magnetic resonance imaging, and diffusion-weighted imaging o...

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Autores principales: Powers, John P., McMillan, Corey T., Brun, Caroline C., Yushkevich, Paul A., Zhang, Hui, Gee, James C., Grossman, Murray
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873600/
https://www.ncbi.nlm.nih.gov/pubmed/24409166
http://dx.doi.org/10.3389/fneur.2013.00212
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author Powers, John P.
McMillan, Corey T.
Brun, Caroline C.
Yushkevich, Paul A.
Zhang, Hui
Gee, James C.
Grossman, Murray
author_facet Powers, John P.
McMillan, Corey T.
Brun, Caroline C.
Yushkevich, Paul A.
Zhang, Hui
Gee, James C.
Grossman, Murray
author_sort Powers, John P.
collection PubMed
description Objective: To relate fractional anisotropy (FA) changes associated with the semantic and logopenic variants of primary progressive aphasia (PPA) to measures of lexical retrieval. Methods: We collected neuropsychological testing, volumetric magnetic resonance imaging, and diffusion-weighted imaging on semantic variant PPA (svPPA) (n = 11) and logopenic variant PPA (lvPPA) (n = 13) patients diagnosed using published criteria. We also acquired neuroimaging data on a group of demographically comparable healthy seniors (n = 34). FA was calculated and analyzed using a white matter (WM) tract-specific analysis approach. This approach utilizes anatomically guided data reduction to increase sensitivity and localizes results within canonically defined tracts. We used non-parametric, cluster-based statistical analysis to relate language performance to FA and determine regions of reduced FA in patients. Results: We found widespread FA reductions in WM for both variants of PPA. FA was related to both confrontation naming and category naming fluency performance in left uncinate fasciculus and corpus callosum in svPPA and left superior and inferior longitudinal fasciculi in lvPPA. Conclusion: SvPPA and lvPPA are associated with distinct disruptions of a large-scale network implicated in lexical retrieval, and the WM disease in each phenotype may contribute to language impairments including lexical retrieval.
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spelling pubmed-38736002014-01-09 White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia Powers, John P. McMillan, Corey T. Brun, Caroline C. Yushkevich, Paul A. Zhang, Hui Gee, James C. Grossman, Murray Front Neurol Neuroscience Objective: To relate fractional anisotropy (FA) changes associated with the semantic and logopenic variants of primary progressive aphasia (PPA) to measures of lexical retrieval. Methods: We collected neuropsychological testing, volumetric magnetic resonance imaging, and diffusion-weighted imaging on semantic variant PPA (svPPA) (n = 11) and logopenic variant PPA (lvPPA) (n = 13) patients diagnosed using published criteria. We also acquired neuroimaging data on a group of demographically comparable healthy seniors (n = 34). FA was calculated and analyzed using a white matter (WM) tract-specific analysis approach. This approach utilizes anatomically guided data reduction to increase sensitivity and localizes results within canonically defined tracts. We used non-parametric, cluster-based statistical analysis to relate language performance to FA and determine regions of reduced FA in patients. Results: We found widespread FA reductions in WM for both variants of PPA. FA was related to both confrontation naming and category naming fluency performance in left uncinate fasciculus and corpus callosum in svPPA and left superior and inferior longitudinal fasciculi in lvPPA. Conclusion: SvPPA and lvPPA are associated with distinct disruptions of a large-scale network implicated in lexical retrieval, and the WM disease in each phenotype may contribute to language impairments including lexical retrieval. Frontiers Media S.A. 2013-12-27 /pmc/articles/PMC3873600/ /pubmed/24409166 http://dx.doi.org/10.3389/fneur.2013.00212 Text en Copyright © 2013 Powers, McMillan, Brun, Yushkevich, Zhang, Gee and Grossman. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Powers, John P.
McMillan, Corey T.
Brun, Caroline C.
Yushkevich, Paul A.
Zhang, Hui
Gee, James C.
Grossman, Murray
White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title_full White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title_fullStr White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title_full_unstemmed White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title_short White Matter Disease Correlates with Lexical Retrieval Deficits in Primary Progressive Aphasia
title_sort white matter disease correlates with lexical retrieval deficits in primary progressive aphasia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873600/
https://www.ncbi.nlm.nih.gov/pubmed/24409166
http://dx.doi.org/10.3389/fneur.2013.00212
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