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Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease
The akinetic/rigid (AR) motor subtype of Parkinson’s Disease is associated with increased rates of motor and cognitive decline. Cross-sectional studies examining the neural correlates of AR have found abnormalities in both subcortical and cortical networks involved in motor planning and execution re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445297/ https://www.ncbi.nlm.nih.gov/pubmed/32885038 http://dx.doi.org/10.1038/s41531-020-00120-3 |
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author | Kann, Sarah J. Chang, Chiapei Manza, Peter Leung, Hoi-Chung |
author_facet | Kann, Sarah J. Chang, Chiapei Manza, Peter Leung, Hoi-Chung |
author_sort | Kann, Sarah J. |
collection | PubMed |
description | The akinetic/rigid (AR) motor subtype of Parkinson’s Disease is associated with increased rates of motor and cognitive decline. Cross-sectional studies examining the neural correlates of AR have found abnormalities in both subcortical and cortical networks involved in motor planning and execution relative to controls. To better understand how these cross-sectional findings are implicated in the unique decline associated with the AR subtype, we examined whether baseline AR symptoms are associated with longitudinal decline of these networks, in contrast to other motor symptoms such as tremor. Using whole brain multiple regression analyses we found that worse AR symptoms at baseline were associated with greater gray matter loss over four years in superior parietal and paracentral lobules and motor cortex. These regions also showed altered connectivity patterns with posterior parietal, premotor, pre-supplementary motor area and dorsolateral prefrontal regions in association with AR symptoms across subjects. Thus, AR symptoms are related to gray matter decline and aberrant functional connectivity in a network of frontal-parietal regions critical for motor planning and execution. These structural and functional abnormalities may therefore be implicated in the more aggressive course of decline associated with the AR relative to tremor-dominant subtype. |
format | Online Article Text |
id | pubmed-7445297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74452972020-09-02 Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease Kann, Sarah J. Chang, Chiapei Manza, Peter Leung, Hoi-Chung NPJ Parkinsons Dis Article The akinetic/rigid (AR) motor subtype of Parkinson’s Disease is associated with increased rates of motor and cognitive decline. Cross-sectional studies examining the neural correlates of AR have found abnormalities in both subcortical and cortical networks involved in motor planning and execution relative to controls. To better understand how these cross-sectional findings are implicated in the unique decline associated with the AR subtype, we examined whether baseline AR symptoms are associated with longitudinal decline of these networks, in contrast to other motor symptoms such as tremor. Using whole brain multiple regression analyses we found that worse AR symptoms at baseline were associated with greater gray matter loss over four years in superior parietal and paracentral lobules and motor cortex. These regions also showed altered connectivity patterns with posterior parietal, premotor, pre-supplementary motor area and dorsolateral prefrontal regions in association with AR symptoms across subjects. Thus, AR symptoms are related to gray matter decline and aberrant functional connectivity in a network of frontal-parietal regions critical for motor planning and execution. These structural and functional abnormalities may therefore be implicated in the more aggressive course of decline associated with the AR relative to tremor-dominant subtype. Nature Publishing Group UK 2020-08-24 /pmc/articles/PMC7445297/ /pubmed/32885038 http://dx.doi.org/10.1038/s41531-020-00120-3 Text en © The Author(s) 2020 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 Kann, Sarah J. Chang, Chiapei Manza, Peter Leung, Hoi-Chung Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title | Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title_full | Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title_fullStr | Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title_full_unstemmed | Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title_short | Akinetic rigid symptoms are associated with decline in a cortical motor network in Parkinson’s disease |
title_sort | akinetic rigid symptoms are associated with decline in a cortical motor network in parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445297/ https://www.ncbi.nlm.nih.gov/pubmed/32885038 http://dx.doi.org/10.1038/s41531-020-00120-3 |
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