Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity

Objectives: Neuroplastic changes that drive recovery of shoulder/elbow function after stoke have been poorly understood. The purpose of this study was to determine the relationship between neuroplastic brain changes related to shoulder/elbow movement control in response to treatment and recovery of...

Full description

Bibliographic Details
Main Authors: Svetlana ePundik, Jessica eMcCabe, Ken eHrovat, Alice E Fredrickson, Curtis eTatsuoka, I Jung eFeng, Janis J Daly
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-07-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00394/full
_version_ 1818149316380852224
author Svetlana ePundik
Svetlana ePundik
Jessica eMcCabe
Ken eHrovat
Alice E Fredrickson
Curtis eTatsuoka
I Jung eFeng
Janis J Daly
Janis J Daly
author_facet Svetlana ePundik
Svetlana ePundik
Jessica eMcCabe
Ken eHrovat
Alice E Fredrickson
Curtis eTatsuoka
I Jung eFeng
Janis J Daly
Janis J Daly
author_sort Svetlana ePundik
collection DOAJ
description Objectives: Neuroplastic changes that drive recovery of shoulder/elbow function after stoke have been poorly understood. The purpose of this study was to determine the relationship between neuroplastic brain changes related to shoulder/elbow movement control in response to treatment and recovery of arm motor function in chronic stroke survivors. Methods: Twenty-three chronic stroke survivors were treated with 12 weeks of arm rehabilitation. Outcome measures included functional Magnetic Resonance Imaging (fMRI) for the shoulder/elbow components of reach and a skilled motor function test (Arm Motor Abilities Test (AMAT)), collected before and after treatment.Results: We observed two patterns of neuroplastic changes that were associated with gains in motor function: decreased or increased task-related brain activation. Those with significantly better motor function at baseline exhibited a decrease in brain activation in response to treatment, evident in the ipsilesional primary motor and contralesional supplementary motor regions; in contrast, those with greater baseline motor impairment, exhibited increased brain activation in response to treatment. There was an linear relationship between greater functional gain (AMAT) and increased activation in bilateral primary motor, contralesional primary and secondary sensory regions, and contralesional lateral premotor area, after adjusting for baseline AMAT, age, and time since stroke. Conclusions: Recovery of functional reach involves recruitment of several contralesional and bilateral primary motor regions. In response to intensive therapy, the direction of functional brain change (i.e. increase or decrease in task-related brain recruitment) for shoulder/elbow reach components depends on baseline level of motor function and may represent either different phases or different strategies of neuroplasticity that drive functional recovery.
first_indexed 2024-12-11T13:05:06Z
format Article
id doaj.art-1bcdc956d63c4a53b677f3ce1b90469d
institution Directory Open Access Journal
issn 1662-5161
language English
last_indexed 2024-12-11T13:05:06Z
publishDate 2015-07-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Human Neuroscience
spelling doaj.art-1bcdc956d63c4a53b677f3ce1b90469d2022-12-22T01:06:21ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612015-07-01910.3389/fnhum.2015.00394135655Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severitySvetlana ePundik0Svetlana ePundik1Jessica eMcCabe2Ken eHrovat3Alice E Fredrickson4Curtis eTatsuoka5I Jung eFeng6Janis J Daly7Janis J Daly8Cleveland Department of Veterans Affairs Medical CenterCase Western Reserve University School of MedicineCleveland Department of Veterans Affairs Medical CenterCleveland Department of Veterans Affairs Medical CenterCleveland Department of Veterans Affairs Medical CenterCase Western Reserve University School of MedicineCase Western Reserve UniveristyMR Gainesville Department of Veterans Affairs Medical CenterUniversity of Florida, College of MedicineObjectives: Neuroplastic changes that drive recovery of shoulder/elbow function after stoke have been poorly understood. The purpose of this study was to determine the relationship between neuroplastic brain changes related to shoulder/elbow movement control in response to treatment and recovery of arm motor function in chronic stroke survivors. Methods: Twenty-three chronic stroke survivors were treated with 12 weeks of arm rehabilitation. Outcome measures included functional Magnetic Resonance Imaging (fMRI) for the shoulder/elbow components of reach and a skilled motor function test (Arm Motor Abilities Test (AMAT)), collected before and after treatment.Results: We observed two patterns of neuroplastic changes that were associated with gains in motor function: decreased or increased task-related brain activation. Those with significantly better motor function at baseline exhibited a decrease in brain activation in response to treatment, evident in the ipsilesional primary motor and contralesional supplementary motor regions; in contrast, those with greater baseline motor impairment, exhibited increased brain activation in response to treatment. There was an linear relationship between greater functional gain (AMAT) and increased activation in bilateral primary motor, contralesional primary and secondary sensory regions, and contralesional lateral premotor area, after adjusting for baseline AMAT, age, and time since stroke. Conclusions: Recovery of functional reach involves recruitment of several contralesional and bilateral primary motor regions. In response to intensive therapy, the direction of functional brain change (i.e. increase or decrease in task-related brain recruitment) for shoulder/elbow reach components depends on baseline level of motor function and may represent either different phases or different strategies of neuroplasticity that drive functional recovery.http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00394/fullStrokefunctional magnetic resonance imagingneuroplasticitymotor learningmotor recoverymotor rehabilitation
spellingShingle Svetlana ePundik
Svetlana ePundik
Jessica eMcCabe
Ken eHrovat
Alice E Fredrickson
Curtis eTatsuoka
I Jung eFeng
Janis J Daly
Janis J Daly
Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
Frontiers in Human Neuroscience
Stroke
functional magnetic resonance imaging
neuroplasticity
motor learning
motor recovery
motor rehabilitation
title Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
title_full Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
title_fullStr Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
title_full_unstemmed Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
title_short Recovery of post stroke proximal arm function, driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
title_sort recovery of post stroke proximal arm function driven by complex neuroplastic bilateral brain activation patterns and predicted by baseline motor dysfunction severity
topic Stroke
functional magnetic resonance imaging
neuroplasticity
motor learning
motor recovery
motor rehabilitation
url http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00394/full
work_keys_str_mv AT svetlanaepundik recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT svetlanaepundik recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT jessicaemccabe recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT kenehrovat recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT aliceefredrickson recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT curtisetatsuoka recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT ijungefeng recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT janisjdaly recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity
AT janisjdaly recoveryofpoststrokeproximalarmfunctiondrivenbycomplexneuroplasticbilateralbrainactivationpatternsandpredictedbybaselinemotordysfunctionseverity