Cargando…

Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease

Beta oscillations within motor-cortical areas have been linked to sensorimotor function. In line with this, pathologically altered beta activity in cortico-basal ganglia pathways has been suggested to contribute to the pathophysiology of Parkinson's disease (PD), a neurodegenerative disorder pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Meissner, Sarah Nadine, Krause, Vanessa, Südmeyer, Martin, Hartmann, Christian Johannes, Pollok, Bettina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849445/
https://www.ncbi.nlm.nih.gov/pubmed/31715558
http://dx.doi.org/10.1016/j.nicl.2019.102057
_version_ 1783469209218449408
author Meissner, Sarah Nadine
Krause, Vanessa
Südmeyer, Martin
Hartmann, Christian Johannes
Pollok, Bettina
author_facet Meissner, Sarah Nadine
Krause, Vanessa
Südmeyer, Martin
Hartmann, Christian Johannes
Pollok, Bettina
author_sort Meissner, Sarah Nadine
collection PubMed
description Beta oscillations within motor-cortical areas have been linked to sensorimotor function. In line with this, pathologically altered beta activity in cortico-basal ganglia pathways has been suggested to contribute to the pathophysiology of Parkinson's disease (PD), a neurodegenerative disorder primarily characterized by motor impairment. Although its precise function is still discussed, beta activity might subserve an anticipatory role in preparation of future actions. By reanalyzing previously published data, we aimed at investigating the role of pre-stimulus motor-cortical beta power modulation in motor sequence learning and its alteration in PD. 20 PD patients and 20 healthy controls (HC) performed a serial reaction time task (SRTT) in which reaction time gain presumably reflects the ability to anticipate subsequent sequence items. Randomly varying patterns served as control trials. Neuromagnetic activity was recorded using magnetoencephalography (MEG) and data was reanalyzed with respect to task stimuli onset. Assuming that pre-stimulus beta power modulation is functionally related to motor sequence learning, reaction time gain due to training on the SRTT should vary depending on the amount of beta power suppression prior to stimulus onset. We hypothesized to find less pre-stimulus beta power suppression in PD patients as compared to HC associated with reduced motor sequence learning in patients. Behavioral analyses revealed that PD patients exhibited smaller reaction time gain in sequence relative to random control trials than HC indicating reduced learning in PD. This finding was indeed paralleled by reduced pre-stimulus beta power suppression in PD patients. Further strengthening its functional relevance, the amount of pre-stimulus beta power suppression during sequence training significantly predicted subsequent reaction time advantage in sequence relative to random trials in patients. In conclusion, the present data provide first evidence for the contribution of pre-stimulus motor-cortical beta power suppression to motor sequence learning and support the hypothesis that beta oscillations may subserve an anticipatory, predictive function, possibly compromised in PD.
format Online
Article
Text
id pubmed-6849445
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-68494452019-11-20 Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease Meissner, Sarah Nadine Krause, Vanessa Südmeyer, Martin Hartmann, Christian Johannes Pollok, Bettina Neuroimage Clin Regular Article Beta oscillations within motor-cortical areas have been linked to sensorimotor function. In line with this, pathologically altered beta activity in cortico-basal ganglia pathways has been suggested to contribute to the pathophysiology of Parkinson's disease (PD), a neurodegenerative disorder primarily characterized by motor impairment. Although its precise function is still discussed, beta activity might subserve an anticipatory role in preparation of future actions. By reanalyzing previously published data, we aimed at investigating the role of pre-stimulus motor-cortical beta power modulation in motor sequence learning and its alteration in PD. 20 PD patients and 20 healthy controls (HC) performed a serial reaction time task (SRTT) in which reaction time gain presumably reflects the ability to anticipate subsequent sequence items. Randomly varying patterns served as control trials. Neuromagnetic activity was recorded using magnetoencephalography (MEG) and data was reanalyzed with respect to task stimuli onset. Assuming that pre-stimulus beta power modulation is functionally related to motor sequence learning, reaction time gain due to training on the SRTT should vary depending on the amount of beta power suppression prior to stimulus onset. We hypothesized to find less pre-stimulus beta power suppression in PD patients as compared to HC associated with reduced motor sequence learning in patients. Behavioral analyses revealed that PD patients exhibited smaller reaction time gain in sequence relative to random control trials than HC indicating reduced learning in PD. This finding was indeed paralleled by reduced pre-stimulus beta power suppression in PD patients. Further strengthening its functional relevance, the amount of pre-stimulus beta power suppression during sequence training significantly predicted subsequent reaction time advantage in sequence relative to random trials in patients. In conclusion, the present data provide first evidence for the contribution of pre-stimulus motor-cortical beta power suppression to motor sequence learning and support the hypothesis that beta oscillations may subserve an anticipatory, predictive function, possibly compromised in PD. Elsevier 2019-10-24 /pmc/articles/PMC6849445/ /pubmed/31715558 http://dx.doi.org/10.1016/j.nicl.2019.102057 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Meissner, Sarah Nadine
Krause, Vanessa
Südmeyer, Martin
Hartmann, Christian Johannes
Pollok, Bettina
Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title_full Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title_fullStr Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title_full_unstemmed Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title_short Pre-stimulus beta power modulation during motor sequence learning is reduced in 'Parkinson's disease
title_sort pre-stimulus beta power modulation during motor sequence learning is reduced in 'parkinson's disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849445/
https://www.ncbi.nlm.nih.gov/pubmed/31715558
http://dx.doi.org/10.1016/j.nicl.2019.102057
work_keys_str_mv AT meissnersarahnadine prestimulusbetapowermodulationduringmotorsequencelearningisreducedinparkinsonsdisease
AT krausevanessa prestimulusbetapowermodulationduringmotorsequencelearningisreducedinparkinsonsdisease
AT sudmeyermartin prestimulusbetapowermodulationduringmotorsequencelearningisreducedinparkinsonsdisease
AT hartmannchristianjohannes prestimulusbetapowermodulationduringmotorsequencelearningisreducedinparkinsonsdisease
AT pollokbettina prestimulusbetapowermodulationduringmotorsequencelearningisreducedinparkinsonsdisease