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Author Notes:

Cathrin M. Buetefisch MD PhD, 1441 Clifton Rd., Atlanta, GA 30322. 404-712-1894. Email: cathrin.buetefisch@emory.edu; 404-712-1894

This work was supported by the National Institute of Neurological Diseases and Stroke, National Institute of Child Development and Health, National Institutes of Health (grant numbers R56NS070879, R01NS090677, 3R01NS090677-04S1). DAB received support from the Emory University NIH/NINDST32 training and translational research in neurology program (T32NS007480), Georgia StrokeNet (1U10NS086607), and the American Heart Association (18POST34060183). DAB is currently at the Department of Kinesiology, University of Georgia, and Augusta University/University of Georgia Medical Partnership, Athens, Georgia. LE received support from the Emory University NIH/NINDST32 training and translational research in neurology program (T32NS007480) and the American Heart Association (18POST34060183).

We thank the participants for their contribution to this study, S. Buetefisch and J. Hudson for technical support, E. Sperin for assistance with regulatory work, and G. Kowalski, A. Caliban, A. Mangin, I. Vernon and I. Chung for assistance with the data collection.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Clinical Neurology
  • Rehabilitation
  • Neurosciences & Neurology
  • stroke
  • motor cortex
  • upper extremity paresis
  • reorganization
  • TMS
  • MRI
  • CORTICOSPINAL TRACT LESION
  • CORTICAL EXCITABILITY
  • HAND FUNCTION
  • RECOVERY
  • BRAIN
  • HEMISPHERE
  • THRESHOLD
  • NORMALIZATION
  • INHIBITION
  • INFARCTION

Stroke Lesion Volume and Injury to Motor Cortex Output Determines Extent of Contralesional Motor Cortex Reorganization

Tools:

Journal Title:

NEUROREHABILITATION AND NEURAL REPAIR

Volume:

Volume 37, Number 2-3

Publisher:

, Pages 119-130

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background: After stroke, increases in contralesional primary motor cortex (M1CL) activity and excitability have been reported. In pre-clinical studies, M1CL reorganization is related to the extent of ipsilesional M1 (M1IL) injury, but this has yet to be tested clinically. Objectives: We tested the hypothesis that the extent of damage to the ipsilesional M1 and/or its corticospinal tract (CST) determines the magnitude of M1CL reorganization and its relationship to affected hand function in humans recovering from stroke. Methods: Thirty-five participants with a single subacute ischemic stroke affecting M1 or CST and hand paresis underwent MRI scans of the brain to measure lesion volume and CST lesion load. Transcranial magnetic stimulation (TMS) of M1IL was used to determine the presence of an electromyographic response (motor evoked potential (MEP+ and MEP−)). M1CL reorganization was determined by TMS applied to M1CL at increasing intensities. Hand function was quantified with the Jebsen Taylor Hand Function Test. Results: The extent of M1CL reorganization was related to greater lesion volume in the MEP− group, but not in the MEP+ group. Greater M1CL reorganization was associated with more impaired hand function in MEP− but not MEP+ participants. Absence of an MEP (MEP−), larger lesion volumes and higher lesion loads in CST, particularly in CST fibers originating in M1 were associated with greater impairment of hand function. Conclusions: In the subacute post-stroke period, stroke volume and M1IL output determine the extent of M1CL reorganization and its relationship to affected hand function, consistent with pre-clinical evidence. ClinicalTrials.gov Identifier: NCT02544503.
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