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Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception

Behavioral studies indicate that persons with Parkinson's disease have complexity dependent problems with the discrimination of auditory rhythms. Furthermore, neuroimaging studies show that rhythm processing activates many brain areas that overlap with areas affected by Parkinson's disease...

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Autores principales: Vikene, Kjetil, Skeie, Geir‐Olve, Specht, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587836/
https://www.ncbi.nlm.nih.gov/pubmed/30375107
http://dx.doi.org/10.1002/hbm.24421
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author Vikene, Kjetil
Skeie, Geir‐Olve
Specht, Karsten
author_facet Vikene, Kjetil
Skeie, Geir‐Olve
Specht, Karsten
author_sort Vikene, Kjetil
collection PubMed
description Behavioral studies indicate that persons with Parkinson's disease have complexity dependent problems with the discrimination of auditory rhythms. Furthermore, neuroimaging studies show that rhythm processing activates many brain areas that overlap with areas affected by Parkinson's disease (PD). This study sought to investigate the neural correlates of rhythm processing in PD and healthy controls, with a particular focus on rhythmic complexity. We further aimed to investigate differences in brain activation during initial phases of rhythm processing. Functional magnetic resonance imaging was used to scan 15 persons with Parkinson's disease and 15 healthy controls while they listened to musical rhythms with two different levels of complexity. Rhythmic complexity had no significant effect on brain activations, but patients and controls showed differences in areas related to temporal auditory processing, notably bilateral planum temporale and inferior parietal lobule. We found indications of a particular sequential or phasic activation pattern of brain activity, where activity in caudate nucleus in the basal ganglia was time‐displaced by activation in the saliency network—comprised of anterior cingulate cortex and bilateral anterior insula—and cortical and subcortical motor areas, during the initial phases of listening to rhythms. We relate our findings to core PD pathology, and discuss the overall, rhythm processing related hyperactivity in PD as a possible dysfunction in specific basal ganglia mechanisms, and the phasic activation pattern in PD as a reflection of a lack of preparatory activation of task‐relevant brain networks for rhythm processing in PD.
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spelling pubmed-65878362019-07-02 Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception Vikene, Kjetil Skeie, Geir‐Olve Specht, Karsten Hum Brain Mapp Research Articles Behavioral studies indicate that persons with Parkinson's disease have complexity dependent problems with the discrimination of auditory rhythms. Furthermore, neuroimaging studies show that rhythm processing activates many brain areas that overlap with areas affected by Parkinson's disease (PD). This study sought to investigate the neural correlates of rhythm processing in PD and healthy controls, with a particular focus on rhythmic complexity. We further aimed to investigate differences in brain activation during initial phases of rhythm processing. Functional magnetic resonance imaging was used to scan 15 persons with Parkinson's disease and 15 healthy controls while they listened to musical rhythms with two different levels of complexity. Rhythmic complexity had no significant effect on brain activations, but patients and controls showed differences in areas related to temporal auditory processing, notably bilateral planum temporale and inferior parietal lobule. We found indications of a particular sequential or phasic activation pattern of brain activity, where activity in caudate nucleus in the basal ganglia was time‐displaced by activation in the saliency network—comprised of anterior cingulate cortex and bilateral anterior insula—and cortical and subcortical motor areas, during the initial phases of listening to rhythms. We relate our findings to core PD pathology, and discuss the overall, rhythm processing related hyperactivity in PD as a possible dysfunction in specific basal ganglia mechanisms, and the phasic activation pattern in PD as a reflection of a lack of preparatory activation of task‐relevant brain networks for rhythm processing in PD. John Wiley & Sons, Inc. 2018-10-29 /pmc/articles/PMC6587836/ /pubmed/30375107 http://dx.doi.org/10.1002/hbm.24421 Text en © 2018 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Vikene, Kjetil
Skeie, Geir‐Olve
Specht, Karsten
Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title_full Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title_fullStr Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title_full_unstemmed Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title_short Abnormal phasic activity in saliency network, motor areas, and basal ganglia in Parkinson's disease during rhythm perception
title_sort abnormal phasic activity in saliency network, motor areas, and basal ganglia in parkinson's disease during rhythm perception
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587836/
https://www.ncbi.nlm.nih.gov/pubmed/30375107
http://dx.doi.org/10.1002/hbm.24421
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