Multifocal transcranial stimulation in chronic ischemic stroke: A phase 1/2a randomized trial.


Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 10 12 2019
revised: 10 02 2020
accepted: 15 03 2020
pubmed: 24 4 2020
medline: 30 9 2020
entrez: 24 4 2020
Statut: ppublish

Résumé

Repetitive transcranial magnetic stimulation (rTMS) may promote recovery of motor function after stroke by inducing functional reorganization of cortical circuits. The objective of this study was to examine whether multifocal cortical stimulation using a new wearable transcranial rotating permanent magnet stimulator (TRPMS) can promote recovery of motor function after stroke by inducing functional reorganization of cortical circuits. Thirty TRPMS treatment was well-tolerated with no device-related adverse effects. Active treatment produced a significantly greater increase in the number of active voxels on fMRI than sham treatment (median +48.5 vs -30, p = 0.038). The median active voxel number after active treatment was 8.8-fold greater than after sham (227.5 vs 26, p = 0.016). Although the statistical power was inadequate to establish clinical endpoint benefits, numerical improvements were demonstrated in 5 of 6 clinical scales of motor function. The treatment effects persisted over a 3-month duration of follow-up. Multifocal bilateral TRPMS was safe and showed significant fMRI changes suggestive of functional reorganization of cortical circuits in patients with chronic ischemic stroke. A larger randomized clinical trial is warranted to verify recovery of motor function.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Repetitive transcranial magnetic stimulation (rTMS) may promote recovery of motor function after stroke by inducing functional reorganization of cortical circuits. The objective of this study was to examine whether multifocal cortical stimulation using a new wearable transcranial rotating permanent magnet stimulator (TRPMS) can promote recovery of motor function after stroke by inducing functional reorganization of cortical circuits.
METHODS METHODS
Thirty
RESULTS RESULTS
TRPMS treatment was well-tolerated with no device-related adverse effects. Active treatment produced a significantly greater increase in the number of active voxels on fMRI than sham treatment (median +48.5 vs -30, p = 0.038). The median active voxel number after active treatment was 8.8-fold greater than after sham (227.5 vs 26, p = 0.016). Although the statistical power was inadequate to establish clinical endpoint benefits, numerical improvements were demonstrated in 5 of 6 clinical scales of motor function. The treatment effects persisted over a 3-month duration of follow-up.
CONCLUSIONS CONCLUSIONS
Multifocal bilateral TRPMS was safe and showed significant fMRI changes suggestive of functional reorganization of cortical circuits in patients with chronic ischemic stroke. A larger randomized clinical trial is warranted to verify recovery of motor function.

Identifiants

pubmed: 32321651
pii: S1052-3057(20)30200-7
doi: 10.1016/j.jstrokecerebrovasdis.2020.104816
pii:
doi:

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

104816

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

David Chiu (D)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States. Electronic address: dchiu@houstonmethodist.org.

C David McCane (CD)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Jason Lee (J)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Blessy John (B)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Lisa Nguyen (L)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Kayla Butler (K)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Rajan Gadhia (R)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Vivek Misra (V)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

John J Volpi (JJ)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Amit Verma (A)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

Santosh A Helekar (SA)

Stanley H. Appel Department of Neurology, Methodist Neurological Institute, Houston Methodist Hospital, 6560 Fannin St #802, Houston, TX 77030, United States.

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Classifications MeSH