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Article: The Discourse Profile in Corticobasal Syndrome: A Comprehensive Clinical and Biomarker Approach

TitleThe Discourse Profile in Corticobasal Syndrome: A Comprehensive Clinical and Biomarker Approach
Authors
Keywordsamyloid-PET
connected speech
corticobasal degeneration
corticobasal syndrome
discourse
language
positron emission tomography
spontaneous speech
Issue Date12-Dec-2022
PublisherMDPI
Citation
Brain Sciences, 2022, v. 12, n. 12 How to Cite?
Abstract

The aim of this study was to characterize the oral discourse of CBS patients and to verify whether measures obtained during a semi-spontaneous speech production could differentiate CBS patients from controls. A second goal was to compare the performance of patients with CBS probably due to Alzheimer’s disease (CBS-AD) pathology and CBS not related to AD (CBS-non-AD) in the same measures, based on the brain metabolic status (FDG-PET) and in the presence of amyloid deposition (amyloid-PET). Results showed that CBS patients were significantly different from controls in speech rate, lexical level, informativeness, and syntactic complexity. Discursive measures did not differentiate CBS-AD from CBS-non-AD. However, CBS-AD displayed more lexical-semantic impairments than controls, a profile that is frequently reported in patients with clinical AD and the logopenic variant of primary progressive aphasia (lvPPA). CBS-non-AD presented mainly with impairments related to motor speech disorders and syntactic complexity, as seen in the non-fluent variant of PPA.


Persistent Identifierhttp://hdl.handle.net/10722/357102
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.796
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorde Almeida, Isabel Junqueira-
dc.contributor.authorSilagi, Marcela Lima-
dc.contributor.authorCarthery-Goulart, Maria Teresa-
dc.contributor.authorParmera, Jacy Bezerra-
dc.contributor.authorCecchini, Mario Amore-
dc.contributor.authorCoutinho, Artur Martins-
dc.contributor.authorDozzi, Brucki Sonia Maria-
dc.contributor.authorNitrini, Ricardo-
dc.contributor.authorSchochat, Eliane-
dc.date.accessioned2025-06-23T08:53:22Z-
dc.date.available2025-06-23T08:53:22Z-
dc.date.issued2022-12-12-
dc.identifier.citationBrain Sciences, 2022, v. 12, n. 12-
dc.identifier.issn2076-3425-
dc.identifier.urihttp://hdl.handle.net/10722/357102-
dc.description.abstract<p>The aim of this study was to characterize the oral discourse of CBS patients and to verify whether measures obtained during a semi-spontaneous speech production could differentiate CBS patients from controls. A second goal was to compare the performance of patients with CBS probably due to Alzheimer’s disease (CBS-AD) pathology and CBS not related to AD (CBS-non-AD) in the same measures, based on the brain metabolic status (FDG-PET) and in the presence of amyloid deposition (amyloid-PET). Results showed that CBS patients were significantly different from controls in speech rate, lexical level, informativeness, and syntactic complexity. Discursive measures did not differentiate CBS-AD from CBS-non-AD. However, CBS-AD displayed more lexical-semantic impairments than controls, a profile that is frequently reported in patients with clinical AD and the logopenic variant of primary progressive aphasia (lvPPA). CBS-non-AD presented mainly with impairments related to motor speech disorders and syntactic complexity, as seen in the non-fluent variant of PPA.<br></p>-
dc.languageeng-
dc.publisherMDPI-
dc.relation.ispartofBrain Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectamyloid-PET-
dc.subjectconnected speech-
dc.subjectcorticobasal degeneration-
dc.subjectcorticobasal syndrome-
dc.subjectdiscourse-
dc.subjectlanguage-
dc.subjectpositron emission tomography-
dc.subjectspontaneous speech-
dc.titleThe Discourse Profile in Corticobasal Syndrome: A Comprehensive Clinical and Biomarker Approach-
dc.typeArticle-
dc.identifier.doi10.3390/brainsci12121705-
dc.identifier.scopuseid_2-s2.0-85144719438-
dc.identifier.volume12-
dc.identifier.issue12-
dc.identifier.eissn2076-3425-
dc.identifier.isiWOS:000900399900001-
dc.identifier.issnl2076-3425-

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