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Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits

INTRODUCTION: Dysfunction in the basal ganglia circuits is a determining factor in the physiopathology of the classic signs of Parkinson's disease (PD) and hypokinetic dysarthria is commonly related to PD. Regarding speech disorders associated with PD, the latest four-level framework of speech...

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Autores principales: Ortiz, Karin Zazo, Brabo, Natalia Casagrande, Minett, Thais Soares C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642417/
https://www.ncbi.nlm.nih.gov/pubmed/29213457
http://dx.doi.org/10.1590/S1980-5764-2016DN1003007
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author Ortiz, Karin Zazo
Brabo, Natalia Casagrande
Minett, Thais Soares C.
author_facet Ortiz, Karin Zazo
Brabo, Natalia Casagrande
Minett, Thais Soares C.
author_sort Ortiz, Karin Zazo
collection PubMed
description INTRODUCTION: Dysfunction in the basal ganglia circuits is a determining factor in the physiopathology of the classic signs of Parkinson's disease (PD) and hypokinetic dysarthria is commonly related to PD. Regarding speech disorders associated with PD, the latest four-level framework of speech complicates the traditional view of dysarthria as a motor execution disorder. Based on findings that dysfunctions in basal ganglia can cause speech disorders, and on the premise that the speech deficits seen in PD are not related to an execution motor disorder alone but also to a disorder at the motor programming level, the main objective of this study was to investigate the presence of sensorimotor disorders of programming (besides the execution disorders previously described) in PD patients. METHODS: A cross-sectional study was conducted in a sample of 60 adults matched for gender, age and education: 30 adult patients diagnosed with idiopathic PD (PDG) and 30 healthy adults (CG). All types of articulation errors were reanalyzed to investigate the nature of these errors. Interjections, hesitations and repetitions of words or sentences (during discourse) were considered typical disfluencies; blocking, episodes of palilalia (words or syllables) were analyzed as atypical disfluencies. We analysed features including successive self-initiated trial, phoneme distortions, self-correction, repetition of sounds and syllables, prolonged movement transitions, additions or omissions of sounds and syllables, in order to identify programming and/or execution failures. Orofacial agility was also investigated. RESULTS: The PDG had worse performance on all sensorimotor speech tasks. All PD patients had hypokinetic dysarthria. CONCLUSION: The clinical characteristics found suggest both execution and programming sensorimotor speech disorders in PD patients.
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spelling pubmed-56424172017-12-06 Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits Ortiz, Karin Zazo Brabo, Natalia Casagrande Minett, Thais Soares C. Dement Neuropsychol Original Articles INTRODUCTION: Dysfunction in the basal ganglia circuits is a determining factor in the physiopathology of the classic signs of Parkinson's disease (PD) and hypokinetic dysarthria is commonly related to PD. Regarding speech disorders associated with PD, the latest four-level framework of speech complicates the traditional view of dysarthria as a motor execution disorder. Based on findings that dysfunctions in basal ganglia can cause speech disorders, and on the premise that the speech deficits seen in PD are not related to an execution motor disorder alone but also to a disorder at the motor programming level, the main objective of this study was to investigate the presence of sensorimotor disorders of programming (besides the execution disorders previously described) in PD patients. METHODS: A cross-sectional study was conducted in a sample of 60 adults matched for gender, age and education: 30 adult patients diagnosed with idiopathic PD (PDG) and 30 healthy adults (CG). All types of articulation errors were reanalyzed to investigate the nature of these errors. Interjections, hesitations and repetitions of words or sentences (during discourse) were considered typical disfluencies; blocking, episodes of palilalia (words or syllables) were analyzed as atypical disfluencies. We analysed features including successive self-initiated trial, phoneme distortions, self-correction, repetition of sounds and syllables, prolonged movement transitions, additions or omissions of sounds and syllables, in order to identify programming and/or execution failures. Orofacial agility was also investigated. RESULTS: The PDG had worse performance on all sensorimotor speech tasks. All PD patients had hypokinetic dysarthria. CONCLUSION: The clinical characteristics found suggest both execution and programming sensorimotor speech disorders in PD patients. Associação de Neurologia Cognitiva e do Comportamento 2016 /pmc/articles/PMC5642417/ /pubmed/29213457 http://dx.doi.org/10.1590/S1980-5764-2016DN1003007 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Articles
Ortiz, Karin Zazo
Brabo, Natalia Casagrande
Minett, Thais Soares C.
Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title_full Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title_fullStr Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title_full_unstemmed Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title_short Sensorimotor speech disorders in Parkinson's disease: Programming and execution deficits
title_sort sensorimotor speech disorders in parkinson's disease: programming and execution deficits
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642417/
https://www.ncbi.nlm.nih.gov/pubmed/29213457
http://dx.doi.org/10.1590/S1980-5764-2016DN1003007
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