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Microstructural alterations predict impaired bimanual control in Parkinson’s disease
Bimanual coordination is impaired in Parkinson’s disease affecting patients’ ability to perform activities of daily living and to maintain independence. Conveyance of information between cortical and subcortical areas is essential for bimanual coordination and relies on the integrity of cerebral mic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185383/ https://www.ncbi.nlm.nih.gov/pubmed/35702729 http://dx.doi.org/10.1093/braincomms/fcac137 |
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author | Loehrer, Philipp A. Weber, Immo Oehrn, Carina R. Nettersheim, Felix S. Dafsari, Haidar S. Knake, Susanne Tittgemeyer, Marc Timmermann, Lars Belke, Marcus |
author_facet | Loehrer, Philipp A. Weber, Immo Oehrn, Carina R. Nettersheim, Felix S. Dafsari, Haidar S. Knake, Susanne Tittgemeyer, Marc Timmermann, Lars Belke, Marcus |
author_sort | Loehrer, Philipp A. |
collection | PubMed |
description | Bimanual coordination is impaired in Parkinson’s disease affecting patients’ ability to perform activities of daily living and to maintain independence. Conveyance of information between cortical and subcortical areas is essential for bimanual coordination and relies on the integrity of cerebral microstructure. As pathological deposition of alpha-synuclein compromises microstructure in Parkinson’s disease, we investigated the relationship between microstructural integrity and bimanual coordination using diffusion-weighted MRI in 23 patients with Parkinson’s disease (mean age ± standard deviation: 56.0 ± 6.45 years; 8 female) and 26 older adults (mean age ± standard deviation: 58.5 ± 5.52 years). Whole-brain analysis revealed specific microstructural alterations between patients and healthy controls matched for age, sex, handedness, and cognitive status congruent with the literature and known Parkinson’s disease pathology. A general linear model revealed distinct microstructural alterations associated with poor bimanual coordination in Parkinson’s disease, corrected for multiple comparisons using a permutation-based approach. Integrating known functional topography, we conclude that distinct changes in microstructure cause an impediment of structures involved in attention, working memory, executive function, motor planning, motor control, and visual processing contributing to impaired bimanual coordination in Parkinson’s disease. |
format | Online Article Text |
id | pubmed-9185383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91853832022-06-13 Microstructural alterations predict impaired bimanual control in Parkinson’s disease Loehrer, Philipp A. Weber, Immo Oehrn, Carina R. Nettersheim, Felix S. Dafsari, Haidar S. Knake, Susanne Tittgemeyer, Marc Timmermann, Lars Belke, Marcus Brain Commun Original Article Bimanual coordination is impaired in Parkinson’s disease affecting patients’ ability to perform activities of daily living and to maintain independence. Conveyance of information between cortical and subcortical areas is essential for bimanual coordination and relies on the integrity of cerebral microstructure. As pathological deposition of alpha-synuclein compromises microstructure in Parkinson’s disease, we investigated the relationship between microstructural integrity and bimanual coordination using diffusion-weighted MRI in 23 patients with Parkinson’s disease (mean age ± standard deviation: 56.0 ± 6.45 years; 8 female) and 26 older adults (mean age ± standard deviation: 58.5 ± 5.52 years). Whole-brain analysis revealed specific microstructural alterations between patients and healthy controls matched for age, sex, handedness, and cognitive status congruent with the literature and known Parkinson’s disease pathology. A general linear model revealed distinct microstructural alterations associated with poor bimanual coordination in Parkinson’s disease, corrected for multiple comparisons using a permutation-based approach. Integrating known functional topography, we conclude that distinct changes in microstructure cause an impediment of structures involved in attention, working memory, executive function, motor planning, motor control, and visual processing contributing to impaired bimanual coordination in Parkinson’s disease. Oxford University Press 2022-05-22 /pmc/articles/PMC9185383/ /pubmed/35702729 http://dx.doi.org/10.1093/braincomms/fcac137 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Loehrer, Philipp A. Weber, Immo Oehrn, Carina R. Nettersheim, Felix S. Dafsari, Haidar S. Knake, Susanne Tittgemeyer, Marc Timmermann, Lars Belke, Marcus Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title | Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title_full | Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title_fullStr | Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title_full_unstemmed | Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title_short | Microstructural alterations predict impaired bimanual control in Parkinson’s disease |
title_sort | microstructural alterations predict impaired bimanual control in parkinson’s disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185383/ https://www.ncbi.nlm.nih.gov/pubmed/35702729 http://dx.doi.org/10.1093/braincomms/fcac137 |
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