Cargando…

Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation

Brain-machine interfaces (BMI) based on scalp EEG have the potential to promote cortical plasticity following stroke, which has been shown to improve motor recovery outcomes. However, the efficacy of BMI enabled robotic training for upper-limb recovery is seldom quantified using clinical, EEG-based,...

Descripción completa

Detalles Bibliográficos
Autores principales: Bhagat, Nikunj A., Yozbatiran, Nuray, Sullivan, Jennifer L., Paranjape, Ruta, Losey, Colin, Hernandez, Zachary, Keser, Zafer, Grossman, Robert, Francisco, Gerard E., O'Malley, Marcia K., Contreras-Vidal, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749405/
https://www.ncbi.nlm.nih.gov/pubmed/33395991
http://dx.doi.org/10.1016/j.nicl.2020.102502
_version_ 1783625295783264256
author Bhagat, Nikunj A.
Yozbatiran, Nuray
Sullivan, Jennifer L.
Paranjape, Ruta
Losey, Colin
Hernandez, Zachary
Keser, Zafer
Grossman, Robert
Francisco, Gerard E.
O'Malley, Marcia K.
Contreras-Vidal, Jose L.
author_facet Bhagat, Nikunj A.
Yozbatiran, Nuray
Sullivan, Jennifer L.
Paranjape, Ruta
Losey, Colin
Hernandez, Zachary
Keser, Zafer
Grossman, Robert
Francisco, Gerard E.
O'Malley, Marcia K.
Contreras-Vidal, Jose L.
author_sort Bhagat, Nikunj A.
collection PubMed
description Brain-machine interfaces (BMI) based on scalp EEG have the potential to promote cortical plasticity following stroke, which has been shown to improve motor recovery outcomes. However, the efficacy of BMI enabled robotic training for upper-limb recovery is seldom quantified using clinical, EEG-based, and kinematics-based metrics. Further, a movement related neural correlate that can predict the extent of motor recovery still remains elusive, which impedes the clinical translation of BMI-based stroke rehabilitation. To address above knowledge gaps, 10 chronic stroke individuals with stable baseline clinical scores were recruited to participate in 12 therapy sessions involving a BMI enabled powered exoskeleton for elbow training. On average, 132 ± 22 repetitions were performed per participant, per session. BMI accuracy across all sessions and subjects was 79 ± 18% with a false positives rate of 23 ± 20%. Post-training clinical assessments found that FMA for upper extremity and ARAT scores significantly improved over baseline by 3.92 ± 3.73 and 5.35 ± 4.62 points, respectively. Also, 80% participants (7 with moderate-mild impairment, 1 with severe impairment) achieved minimal clinically important difference (MCID: FMA-UE >5.2 or ARAT >5.7) during the course of the study. Kinematic measures indicate that, on average, participants’ movements became faster and smoother. Moreover, modulations in movement related cortical potentials, an EEG-based neural correlate measured contralateral to the impaired arm, were significantly correlated with ARAT scores (ρ = 0.72, p < 0.05) and marginally correlated with FMA-UE (ρ = 0.63, p = 0.051). This suggests higher activation of ipsi-lesional hemisphere post-intervention or inhibition of competing contra-lesional hemisphere, which may be evidence of neuroplasticity and cortical reorganization following BMI mediated rehabilitation therapy.
format Online
Article
Text
id pubmed-7749405
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-77494052020-12-22 Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation Bhagat, Nikunj A. Yozbatiran, Nuray Sullivan, Jennifer L. Paranjape, Ruta Losey, Colin Hernandez, Zachary Keser, Zafer Grossman, Robert Francisco, Gerard E. O'Malley, Marcia K. Contreras-Vidal, Jose L. Neuroimage Clin Articles from the Special Issue on on "Imaging-based biomarkers in psychiatry – diagnosis, prognosis, outcomes" edited by Claire Wilcox and Vince Calhoun Brain-machine interfaces (BMI) based on scalp EEG have the potential to promote cortical plasticity following stroke, which has been shown to improve motor recovery outcomes. However, the efficacy of BMI enabled robotic training for upper-limb recovery is seldom quantified using clinical, EEG-based, and kinematics-based metrics. Further, a movement related neural correlate that can predict the extent of motor recovery still remains elusive, which impedes the clinical translation of BMI-based stroke rehabilitation. To address above knowledge gaps, 10 chronic stroke individuals with stable baseline clinical scores were recruited to participate in 12 therapy sessions involving a BMI enabled powered exoskeleton for elbow training. On average, 132 ± 22 repetitions were performed per participant, per session. BMI accuracy across all sessions and subjects was 79 ± 18% with a false positives rate of 23 ± 20%. Post-training clinical assessments found that FMA for upper extremity and ARAT scores significantly improved over baseline by 3.92 ± 3.73 and 5.35 ± 4.62 points, respectively. Also, 80% participants (7 with moderate-mild impairment, 1 with severe impairment) achieved minimal clinically important difference (MCID: FMA-UE >5.2 or ARAT >5.7) during the course of the study. Kinematic measures indicate that, on average, participants’ movements became faster and smoother. Moreover, modulations in movement related cortical potentials, an EEG-based neural correlate measured contralateral to the impaired arm, were significantly correlated with ARAT scores (ρ = 0.72, p < 0.05) and marginally correlated with FMA-UE (ρ = 0.63, p = 0.051). This suggests higher activation of ipsi-lesional hemisphere post-intervention or inhibition of competing contra-lesional hemisphere, which may be evidence of neuroplasticity and cortical reorganization following BMI mediated rehabilitation therapy. Elsevier 2020-11-19 /pmc/articles/PMC7749405/ /pubmed/33395991 http://dx.doi.org/10.1016/j.nicl.2020.102502 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles from the Special Issue on on "Imaging-based biomarkers in psychiatry – diagnosis, prognosis, outcomes" edited by Claire Wilcox and Vince Calhoun
Bhagat, Nikunj A.
Yozbatiran, Nuray
Sullivan, Jennifer L.
Paranjape, Ruta
Losey, Colin
Hernandez, Zachary
Keser, Zafer
Grossman, Robert
Francisco, Gerard E.
O'Malley, Marcia K.
Contreras-Vidal, Jose L.
Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title_full Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title_fullStr Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title_full_unstemmed Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title_short Neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
title_sort neural activity modulations and motor recovery following brain-exoskeleton interface mediated stroke rehabilitation
topic Articles from the Special Issue on on "Imaging-based biomarkers in psychiatry – diagnosis, prognosis, outcomes" edited by Claire Wilcox and Vince Calhoun
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749405/
https://www.ncbi.nlm.nih.gov/pubmed/33395991
http://dx.doi.org/10.1016/j.nicl.2020.102502
work_keys_str_mv AT bhagatnikunja neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT yozbatirannuray neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT sullivanjenniferl neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT paranjaperuta neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT loseycolin neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT hernandezzachary neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT keserzafer neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT grossmanrobert neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT franciscogerarde neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT omalleymarciak neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation
AT contrerasvidaljosel neuralactivitymodulationsandmotorrecoveryfollowingbrainexoskeletoninterfacemediatedstrokerehabilitation