Eeva Parkkonen1,2,3, Kristina Laaksonen1,2,3, Harri Piitulainen1, Johanna Pekkola4, Lauri Parkkonen1, Turgut Tatlisumak2,3,5,6, Nina Forss1,2,3. 1. 1 Department of Neuroscience and Biomedical Engineering, Aalto University School of Science, Espoo, Finland. 2. 2 Department of Neurology, Helsinki University Hospital, Helsinki, Finland. 3. 3 Clinical Neurosciences, University of Helsinki, Helsinki, Finland. 4. 4 HUS Medical Imaging Center, Radiology, University of Helsinki and Helsinki University Hospital, Finland. 5. 5 Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden. 6. 6 Department of Clinical Neurosciences, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Abstract
BACKGROUND: Stroke is a major cause of disability worldwide, and effective rehabilitation is crucial to regain skills for independent living. Recently, novel therapeutic approaches manipulating the excitatory-inhibitory balance of the motor cortex have been introduced to boost recovery after stroke. However, stroke-induced neurophysiological changes of the motor cortex may vary despite of similar clinical symptoms. Therefore, better understanding of excitability changes after stroke is essential when developing and targeting novel therapeutic approaches. OBJECTIVE AND METHODS: We identified recovery-related alterations in motor cortex excitability after stroke using magnetoencephalography. Dynamics (suppression and rebound) of the ~20-Hz motor cortex rhythm were monitored during passive movement of the index finger in 23 stroke patients with upper limb paresis at acute phase, 1 month, and 1 year after stroke. RESULTS: After stroke, the strength of the ~20-Hz rebound to stimulation of both impaired and healthy hand was decreased with respect to the controls in the affected (AH) and unaffected (UH) hemispheres, and increased during recovery. Importantly, the rebound strength was lower than that of the controls in the AH and UH also to healthy-hand stimulation despite of intact afferent input. In the AH, the rebound strength to impaired-hand stimulation correlated with hand motor recovery. CONCLUSIONS: Motor cortex excitability is increased bilaterally after stroke and decreases concomitantly with recovery. Motor cortex excitability changes are related to both alterations in local excitatory-inhibitory circuits and changes in afferent input. Fluent sensorimotor integration, which is closely coupled with excitability changes, seems to be a key factor for motor recovery.
BACKGROUND:Stroke is a major cause of disability worldwide, and effective rehabilitation is crucial to regain skills for independent living. Recently, novel therapeutic approaches manipulating the excitatory-inhibitory balance of the motor cortex have been introduced to boost recovery after stroke. However, stroke-induced neurophysiological changes of the motor cortex may vary despite of similar clinical symptoms. Therefore, better understanding of excitability changes after stroke is essential when developing and targeting novel therapeutic approaches. OBJECTIVE AND METHODS: We identified recovery-related alterations in motor cortex excitability after stroke using magnetoencephalography. Dynamics (suppression and rebound) of the ~20-Hz motor cortex rhythm were monitored during passive movement of the index finger in 23 strokepatients with upper limb paresis at acute phase, 1 month, and 1 year after stroke. RESULTS: After stroke, the strength of the ~20-Hz rebound to stimulation of both impaired and healthy hand was decreased with respect to the controls in the affected (AH) and unaffected (UH) hemispheres, and increased during recovery. Importantly, the rebound strength was lower than that of the controls in the AH and UH also to healthy-hand stimulation despite of intact afferent input. In the AH, the rebound strength to impaired-hand stimulation correlated with hand motor recovery. CONCLUSIONS: Motor cortex excitability is increased bilaterally after stroke and decreases concomitantly with recovery. Motor cortex excitability changes are related to both alterations in local excitatory-inhibitory circuits and changes in afferent input. Fluent sensorimotor integration, which is closely coupled with excitability changes, seems to be a key factor for motor recovery.
Authors: Sarah B Zandvliet; Erwin E H van Wegen; S Floor Campfens; Herman van der Kooij; Gert Kwakkel; Carel G M Meskers Journal: Neurorehabil Neural Repair Date: 2020-03-04 Impact factor: 3.919
Authors: Joshua P Kulasingham; Christian Brodbeck; Sheena Khan; Elisabeth B Marsh; Jonathan Z Simon Journal: Front Neurol Date: 2022-03-28 Impact factor: 4.003
Authors: Jukka Vanhanen; Lauri Parkkonen; Jyrki P Mäkelä; Alexandra Tolmacheva; Anastasia Shulga; Andrey Rodionov; Erika Kirveskari Journal: Spinal Cord Ser Cases Date: 2022-04-05
Authors: Daisie O Pakenham; Andrew J Quinn; Adam Fry; Susan T Francis; Mark W Woolrich; Matthew J Brookes; Karen J Mullinger Journal: Neuroimage Date: 2019-10-22 Impact factor: 6.556