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Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis

Brain stimulation combined with intensive therapy may improve hand function in children with perinatal stroke‐induced unilateral cerebral palsy (UCP). However, response to therapy varies and underlying neuroplasticity mechanisms remain unclear. Here, we aimed to characterize robotic motor mapping ou...

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Autores principales: Kuo, Hsing‐Ching, Zewdie, Ephrem, Giuffre, Adrianna, Gan, Liu Shi, Carlson, Helen L., Wrightson, James, Kirton, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294290/
https://www.ncbi.nlm.nih.gov/pubmed/35451540
http://dx.doi.org/10.1002/hbm.25881
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author Kuo, Hsing‐Ching
Zewdie, Ephrem
Giuffre, Adrianna
Gan, Liu Shi
Carlson, Helen L.
Wrightson, James
Kirton, Adam
author_facet Kuo, Hsing‐Ching
Zewdie, Ephrem
Giuffre, Adrianna
Gan, Liu Shi
Carlson, Helen L.
Wrightson, James
Kirton, Adam
author_sort Kuo, Hsing‐Ching
collection PubMed
description Brain stimulation combined with intensive therapy may improve hand function in children with perinatal stroke‐induced unilateral cerebral palsy (UCP). However, response to therapy varies and underlying neuroplasticity mechanisms remain unclear. Here, we aimed to characterize robotic motor mapping outcomes in children with UCP. Twenty‐nine children with perinatal stroke and UCP (median age 11 ± 2 years) were compared to 24 typically developing controls (TDC). Robotic, neuronavigated transcranial magnetic stimulation was employed to define bilateral motor maps including area, volume, and peak motor evoked potential (MEP). Map outcomes were compared to the primary clinical outcome of the Jebsen–Taylor Test of Hand Function (JTT). Maps were reliably obtained in the contralesional motor cortex (24/29) but challenging in the lesioned hemisphere (5/29). Within the contralesional M1 of participants with UCP, area and peak MEP amplitude of the unaffected map were larger than the affected map. When comparing bilateral maps within the contralesional M1 in children with UCP to that of TDC, only peak MEP amplitudes were different, being smaller for the affected hand as compared to TDC. We observed correlations between the unaffected map when stimulating the contralesional M1 and function of the unaffected hand. Robotic motor mapping can characterize motor cortex neurophysiology in children with perinatal stroke. Map area and peak MEP amplitude may represent discrete biomarkers of developmental plasticity in the contralesional M1. Correlations between map metrics and hand function suggest clinical relevance and utility in studies of interventional plasticity.
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spelling pubmed-92942902022-07-20 Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis Kuo, Hsing‐Ching Zewdie, Ephrem Giuffre, Adrianna Gan, Liu Shi Carlson, Helen L. Wrightson, James Kirton, Adam Hum Brain Mapp Research Articles Brain stimulation combined with intensive therapy may improve hand function in children with perinatal stroke‐induced unilateral cerebral palsy (UCP). However, response to therapy varies and underlying neuroplasticity mechanisms remain unclear. Here, we aimed to characterize robotic motor mapping outcomes in children with UCP. Twenty‐nine children with perinatal stroke and UCP (median age 11 ± 2 years) were compared to 24 typically developing controls (TDC). Robotic, neuronavigated transcranial magnetic stimulation was employed to define bilateral motor maps including area, volume, and peak motor evoked potential (MEP). Map outcomes were compared to the primary clinical outcome of the Jebsen–Taylor Test of Hand Function (JTT). Maps were reliably obtained in the contralesional motor cortex (24/29) but challenging in the lesioned hemisphere (5/29). Within the contralesional M1 of participants with UCP, area and peak MEP amplitude of the unaffected map were larger than the affected map. When comparing bilateral maps within the contralesional M1 in children with UCP to that of TDC, only peak MEP amplitudes were different, being smaller for the affected hand as compared to TDC. We observed correlations between the unaffected map when stimulating the contralesional M1 and function of the unaffected hand. Robotic motor mapping can characterize motor cortex neurophysiology in children with perinatal stroke. Map area and peak MEP amplitude may represent discrete biomarkers of developmental plasticity in the contralesional M1. Correlations between map metrics and hand function suggest clinical relevance and utility in studies of interventional plasticity. John Wiley & Sons, Inc. 2022-04-22 /pmc/articles/PMC9294290/ /pubmed/35451540 http://dx.doi.org/10.1002/hbm.25881 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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
Kuo, Hsing‐Ching
Zewdie, Ephrem
Giuffre, Adrianna
Gan, Liu Shi
Carlson, Helen L.
Wrightson, James
Kirton, Adam
Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title_full Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title_fullStr Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title_full_unstemmed Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title_short Robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
title_sort robotic mapping of motor cortex in children with perinatal stroke and hemiparesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294290/
https://www.ncbi.nlm.nih.gov/pubmed/35451540
http://dx.doi.org/10.1002/hbm.25881
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