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Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment
Individuals with Parkinson’s disease (PD) experience rhythm disorders in a number of motor tasks, such as (i) oral diadochokinesis, (ii) finger tapping, and (iii) gait. These common motor deficits may be signs of “general dysrhythmia”, a central disorder spanning across effectors and tasks, and pote...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761142/ https://www.ncbi.nlm.nih.gov/pubmed/31583269 http://dx.doi.org/10.1038/s41531-019-0092-6 |
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author | Puyjarinet, Frédéric Bégel, Valentin Gény, Christian Driss, Valérie Cuartero, Marie-Charlotte Kotz, Sonja A. Pinto, Serge Dalla Bella, Simone |
author_facet | Puyjarinet, Frédéric Bégel, Valentin Gény, Christian Driss, Valérie Cuartero, Marie-Charlotte Kotz, Sonja A. Pinto, Serge Dalla Bella, Simone |
author_sort | Puyjarinet, Frédéric |
collection | PubMed |
description | Individuals with Parkinson’s disease (PD) experience rhythm disorders in a number of motor tasks, such as (i) oral diadochokinesis, (ii) finger tapping, and (iii) gait. These common motor deficits may be signs of “general dysrhythmia”, a central disorder spanning across effectors and tasks, and potentially sharing the same neural substrate. However, to date, little is known about the relationship between rhythm impairments across domains and effectors. To test this hypothesis, we assessed whether rhythmic disturbances in three different domains (i.e., orofacial, manual, and gait) can be related in PD. Moreover, we investigated whether rhythmic motor performance across these domains can be predicted by rhythm perception, a measure of central rhythmic processing not confounded with motor output. Twenty-two PD patients (mean age: 69.5 ± 5.44) participated in the study. They underwent neurological and neuropsychological assessments, and they performed three rhythmic motor tasks. For oral diadochokinesia, participants had to repeatedly produce a trisyllable pseudoword. For gait, they walked along a computerized walkway. For the manual task, patients had to repeatedly produce finger taps. The first two rhythmic motor tasks were unpaced, and the manual tapping task was performed both without a pacing stimulus and musically paced. Rhythm perception was also tested. We observed that rhythmic variability of motor performances (inter-syllable, inter-tap, and inter-stride time error) was related between the three functions. Moreover, rhythmic performance was predicted by rhythm perception abilities, as demonstrated with a logistic regression model. Hence, rhythm impairments in different motor domains are found to be related in PD and may be underpinned by a common impaired central rhythm mechanism, revealed by a deficit in rhythm perception. These results may provide a novel perspective on how interpret the effects of rhythm-based interventions in PD, within and across motor domains. |
format | Online Article Text |
id | pubmed-6761142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67611422019-10-03 Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment Puyjarinet, Frédéric Bégel, Valentin Gény, Christian Driss, Valérie Cuartero, Marie-Charlotte Kotz, Sonja A. Pinto, Serge Dalla Bella, Simone NPJ Parkinsons Dis Article Individuals with Parkinson’s disease (PD) experience rhythm disorders in a number of motor tasks, such as (i) oral diadochokinesis, (ii) finger tapping, and (iii) gait. These common motor deficits may be signs of “general dysrhythmia”, a central disorder spanning across effectors and tasks, and potentially sharing the same neural substrate. However, to date, little is known about the relationship between rhythm impairments across domains and effectors. To test this hypothesis, we assessed whether rhythmic disturbances in three different domains (i.e., orofacial, manual, and gait) can be related in PD. Moreover, we investigated whether rhythmic motor performance across these domains can be predicted by rhythm perception, a measure of central rhythmic processing not confounded with motor output. Twenty-two PD patients (mean age: 69.5 ± 5.44) participated in the study. They underwent neurological and neuropsychological assessments, and they performed three rhythmic motor tasks. For oral diadochokinesia, participants had to repeatedly produce a trisyllable pseudoword. For gait, they walked along a computerized walkway. For the manual task, patients had to repeatedly produce finger taps. The first two rhythmic motor tasks were unpaced, and the manual tapping task was performed both without a pacing stimulus and musically paced. Rhythm perception was also tested. We observed that rhythmic variability of motor performances (inter-syllable, inter-tap, and inter-stride time error) was related between the three functions. Moreover, rhythmic performance was predicted by rhythm perception abilities, as demonstrated with a logistic regression model. Hence, rhythm impairments in different motor domains are found to be related in PD and may be underpinned by a common impaired central rhythm mechanism, revealed by a deficit in rhythm perception. These results may provide a novel perspective on how interpret the effects of rhythm-based interventions in PD, within and across motor domains. Nature Publishing Group UK 2019-09-25 /pmc/articles/PMC6761142/ /pubmed/31583269 http://dx.doi.org/10.1038/s41531-019-0092-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Puyjarinet, Frédéric Bégel, Valentin Gény, Christian Driss, Valérie Cuartero, Marie-Charlotte Kotz, Sonja A. Pinto, Serge Dalla Bella, Simone Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title | Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title_full | Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title_fullStr | Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title_full_unstemmed | Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title_short | Heightened orofacial, manual, and gait variability in Parkinson’s disease results from a general rhythmic impairment |
title_sort | heightened orofacial, manual, and gait variability in parkinson’s disease results from a general rhythmic impairment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761142/ https://www.ncbi.nlm.nih.gov/pubmed/31583269 http://dx.doi.org/10.1038/s41531-019-0092-6 |
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