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Clinical Profile of PiB-Positive Corticobasal Syndrome

BACKGROUND: Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer’s pathology, have been described in association with CBS. The present study aimed to estab...

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Autores principales: Burrell, James R., Hornberger, Michael, Villemagne, Victor L., Rowe, Christopher C., Hodges, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618463/
https://www.ncbi.nlm.nih.gov/pubmed/23577184
http://dx.doi.org/10.1371/journal.pone.0061025
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author Burrell, James R.
Hornberger, Michael
Villemagne, Victor L.
Rowe, Christopher C.
Hodges, John R.
author_facet Burrell, James R.
Hornberger, Michael
Villemagne, Victor L.
Rowe, Christopher C.
Hodges, John R.
author_sort Burrell, James R.
collection PubMed
description BACKGROUND: Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer’s pathology, have been described in association with CBS. The present study aimed to establish clinical, neuropsychological, and neuroimaging features that could be useful in the distinction of CBS due to AD pathology from other CBS cases in life based on [(11)C] Pittsburgh Compound B positron emission tomography (PiB-PET) status. METHODS: Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer’s pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared. RESULTS: Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/−6.9 years; median symptom duration was 35.5+/−22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus. CONCLUSIONS: Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology.
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spelling pubmed-36184632013-04-10 Clinical Profile of PiB-Positive Corticobasal Syndrome Burrell, James R. Hornberger, Michael Villemagne, Victor L. Rowe, Christopher C. Hodges, John R. PLoS One Research Article BACKGROUND: Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer’s pathology, have been described in association with CBS. The present study aimed to establish clinical, neuropsychological, and neuroimaging features that could be useful in the distinction of CBS due to AD pathology from other CBS cases in life based on [(11)C] Pittsburgh Compound B positron emission tomography (PiB-PET) status. METHODS: Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer’s pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared. RESULTS: Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/−6.9 years; median symptom duration was 35.5+/−22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus. CONCLUSIONS: Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology. Public Library of Science 2013-04-05 /pmc/articles/PMC3618463/ /pubmed/23577184 http://dx.doi.org/10.1371/journal.pone.0061025 Text en © 2013 Burrell et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Burrell, James R.
Hornberger, Michael
Villemagne, Victor L.
Rowe, Christopher C.
Hodges, John R.
Clinical Profile of PiB-Positive Corticobasal Syndrome
title Clinical Profile of PiB-Positive Corticobasal Syndrome
title_full Clinical Profile of PiB-Positive Corticobasal Syndrome
title_fullStr Clinical Profile of PiB-Positive Corticobasal Syndrome
title_full_unstemmed Clinical Profile of PiB-Positive Corticobasal Syndrome
title_short Clinical Profile of PiB-Positive Corticobasal Syndrome
title_sort clinical profile of pib-positive corticobasal syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618463/
https://www.ncbi.nlm.nih.gov/pubmed/23577184
http://dx.doi.org/10.1371/journal.pone.0061025
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