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Stratifying chronic stroke patients based on the influence of contralesional motor cortices: An inter-hemispheric inhibition study

Authors :
Andre G. Machado
Kenneth Earl Sakaie
Vishwanath Sankarasubramanian
Manshi Li
Ela B. Plow
Xiaofeng Wang
Stephen E. Jones
Kelsey A. Potter-Baker
David A. Cunningham
John Lee
Yin Liang Lin
Source :
Clinical Neurophysiology. 131:2516-2525
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Objective A recent “bimodal-balance recovery” model suggests that contralesional influence varies based on the amount of ipsilesional reserve: inhibitory when there is a large reserve, but supportive when there is a low reserve. Here, we investigated the relationships between contralesional influence (inter-hemispheric inhibition, IHI) and ipsilesional reserve (corticospinal damage/impairment), and also defined a criterion separating subgroups based on the relationships. Methods Twenty-four patients underwent assessment of IHI using Transcranial Magnetic Stimulation (ipsilateral silent period method), motor impairment using Upper Extremity Fugl-Meyer (UEFM), and corticospinal damage using Diffusion Tensor Imaging and active motor threshold. Assessments of UEFM and IHI were repeated after 5-week rehabilitation (n = 21). Results Relationship between IHI and baseline UEFM was quadratic with criterion at UEFM 43 (95%conference interval: 40–46). Patients less impaired than UEFM = 43 showed stronger IHI with more impairment, whereas patients more impaired than UEFM = 43 showed lower IHI with more impairment. Of those made clinically-meaningful functional gains in rehabilitation (n = 14), more-impaired patients showed further IHI reduction. Conclusions A criterion impairment-level can be derived to stratify patient-subgroups based on the bimodal influence of contralesional cortex. Contralesional influence also evolves differently across subgroups following rehabilitation. Significance The criterion may be used to stratify patients to design targeted, precision treatments.

Details

ISSN :
13882457
Volume :
131
Database :
OpenAIRE
Journal :
Clinical Neurophysiology
Accession number :
edsair.doi...........e235fb8389c2fa12836825687e438324
Full Text :
https://doi.org/10.1016/j.clinph.2020.06.016