Cargando…
Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy
OBJECTIVE: It is widely believed that the perinatal brain injuries seen in youth with cerebral palsy (CP) impact neuronal processing of sensory information and the production of leg motor actions during gait. However, very limited efforts have been made to evaluate the connection between neural acti...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732255/ https://www.ncbi.nlm.nih.gov/pubmed/33174692 http://dx.doi.org/10.1002/acn3.51246 |
_version_ | 1783622052608999424 |
---|---|
author | Kurz, Max J. Bergwell, Hannah Spooner, Rachel Baker, Sarah Heinrichs‐Graham, Elizabeth Wilson, Tony W. |
author_facet | Kurz, Max J. Bergwell, Hannah Spooner, Rachel Baker, Sarah Heinrichs‐Graham, Elizabeth Wilson, Tony W. |
author_sort | Kurz, Max J. |
collection | PubMed |
description | OBJECTIVE: It is widely believed that the perinatal brain injuries seen in youth with cerebral palsy (CP) impact neuronal processing of sensory information and the production of leg motor actions during gait. However, very limited efforts have been made to evaluate the connection between neural activity within sensorimotor networks and the altered spatiotemportal gait biomechanics seen in youth with CP. The objective of this investigation was to use magnetoencephalographic (MEG) brain imaging and biomechanical analysis to probe this connection. METHODS: We examined the cortical beta oscillations serving motor control of the legs in a cohort of youth with CP (N = 20; Age = 15.5 ± 3 years; GMFCS levels I‐III) and healthy controls (N = 15; Age = 14.1 ± 3 years) using MEG brain imaging and a goal‐directed isometric knee target‐matching task. Outside the scanner, a digital mat was used to quantify the spatiotemporal gait biomechanics. RESULTS: Our MEG imaging results revealed that the participants with CP exhibited stronger sensorimotor beta oscillations during the motor planning and execution stages compared to the controls. Interestingly, we also found that those with the strongest sensorimotor beta oscillations during motor execution also tended to walk slower and have a reduced cadence. INTERPRETATION: These results fuel the impression that the beta sensorimotor cortical oscillations that underlie leg musculature control may play a central role in the altered mobility seen in youth with CP. |
format | Online Article Text |
id | pubmed-7732255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77322552020-12-16 Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy Kurz, Max J. Bergwell, Hannah Spooner, Rachel Baker, Sarah Heinrichs‐Graham, Elizabeth Wilson, Tony W. Ann Clin Transl Neurol Research Articles OBJECTIVE: It is widely believed that the perinatal brain injuries seen in youth with cerebral palsy (CP) impact neuronal processing of sensory information and the production of leg motor actions during gait. However, very limited efforts have been made to evaluate the connection between neural activity within sensorimotor networks and the altered spatiotemportal gait biomechanics seen in youth with CP. The objective of this investigation was to use magnetoencephalographic (MEG) brain imaging and biomechanical analysis to probe this connection. METHODS: We examined the cortical beta oscillations serving motor control of the legs in a cohort of youth with CP (N = 20; Age = 15.5 ± 3 years; GMFCS levels I‐III) and healthy controls (N = 15; Age = 14.1 ± 3 years) using MEG brain imaging and a goal‐directed isometric knee target‐matching task. Outside the scanner, a digital mat was used to quantify the spatiotemporal gait biomechanics. RESULTS: Our MEG imaging results revealed that the participants with CP exhibited stronger sensorimotor beta oscillations during the motor planning and execution stages compared to the controls. Interestingly, we also found that those with the strongest sensorimotor beta oscillations during motor execution also tended to walk slower and have a reduced cadence. INTERPRETATION: These results fuel the impression that the beta sensorimotor cortical oscillations that underlie leg musculature control may play a central role in the altered mobility seen in youth with CP. John Wiley and Sons Inc. 2020-11-11 /pmc/articles/PMC7732255/ /pubmed/33174692 http://dx.doi.org/10.1002/acn3.51246 Text en © 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association 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 Kurz, Max J. Bergwell, Hannah Spooner, Rachel Baker, Sarah Heinrichs‐Graham, Elizabeth Wilson, Tony W. Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title | Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title_full | Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title_fullStr | Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title_full_unstemmed | Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title_short | Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
title_sort | motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732255/ https://www.ncbi.nlm.nih.gov/pubmed/33174692 http://dx.doi.org/10.1002/acn3.51246 |
work_keys_str_mv | AT kurzmaxj motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy AT bergwellhannah motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy AT spoonerrachel motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy AT bakersarah motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy AT heinrichsgrahamelizabeth motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy AT wilsontonyw motorbetacorticaloscillationsarerelatedwiththegaitkinematicsofyouthwithcerebralpalsy |