Phase-dependent local brain states determine the impact of image-guided transcranial magnetic stimulation on motor network electroencephalographic synchronization.


Journal

The Journal of physiology
ISSN: 1469-7793
Titre abrégé: J Physiol
Pays: England
ID NLM: 0266262

Informations de publication

Date de publication:
03 2022
Historique:
received: 19 09 2021
accepted: 10 11 2021
pubmed: 21 11 2021
medline: 3 5 2022
entrez: 20 11 2021
Statut: ppublish

Résumé

Recent studies have synchronized transcranial magnetic stimulation (TMS) application with pre-defined brain oscillatory phases showing how brain response to perturbation depends on the brain state. However, none have investigated whether phase-dependent TMS can possibly modulate connectivity with homologous distant brain regions belonging to the same network. In the framework of network-targeted TMS, we investigated whether stimulation delivered at a specific phase of ongoing brain oscillations might favour stronger cortico-cortical (c-c) synchronization of distant network nodes connected to the stimulation target. Neuronavigated TMS pulses were delivered over the primary motor cortex (M1) during ongoing electroencephalography recording in 24 healthy individuals over two repeated sessions 1 month apart. Stimulation effects were analysed considering whether the TMS pulse was delivered at the time of a positive (peak) or negative (trough) phase of μ-frequency oscillation, which determines c-c synchrony within homologous areas of the sensorimotor network. Diffusion weighted imaging was used to study c-c connectivity within the sensorimotor network and identify contralateral regions connected with the stimulation spot. Depending on when during the μ-activity the TMS-pulse was applied (peak or trough), its impact on inter-hemispheric network synchrony varied significantly. Higher M1-M1 phase-lock synchronization after the TMS-pulse (0-200 ms) in the μ-frequency band was found for trough compared to peak stimulation trials in both study visits. Phase-dependent TMS delivery might be crucial not only to amplify local effects but also to increase the magnitude and reliability of the response to the external perturbation, with implications for interventions aimed at engaging more distributed functional brain networks. KEY POINTS: Synchronized transcranial magnetic stimulation (TMS) pulses with pre-defined brain oscillatory phases allow evaluation of the impact of brain states on TMS effects. TMS pulses over M1 at the negative peak of the μ-frequency band induce higher phase-lock synchronization with interconnected contralateral homologous regions. Cortico-cortical synchronization changes are linearly predicted by the fibre density and cross-section of the white matter tract that connects the two brain regions. Phase-dependent TMS delivery might be crucial not only to amplify local effects but also to increase the magnitude and reliability of within-network synchronization.

Identifiants

pubmed: 34799873
doi: 10.1113/JP282393
pmc: PMC9728936
mid: NIHMS1832370
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1455-1471

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH115949
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG060987
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH117063
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG060981
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG031720
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG059089
Pays : United States

Informations de copyright

© 2021 The Authors. The Journal of Physiology © 2021 The Physiological Society.

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Auteurs

Davide Momi (D)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Department of Neuroscience, Imaging and Clinical Sciences, University of Chieti-Pescara, Chieti, Italy.

Recep A Ozdemir (RA)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.

Ehsan Tadayon (E)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.

Pierre Boucher (P)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.

Alberto Di Domenico (A)

Department of Psychological Science, Humanities and Territory, University of Chieti-Pescara, Chieti, Italy.

Mirco Fasolo (M)

Department of Psychological Science, Humanities and Territory, University of Chieti-Pescara, Chieti, Italy.

Mouhsin M Shafi (MM)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Department of Neurology, Harvard Medical School, Boston, MA, USA.

Alvaro Pascual-Leone (A)

Hinda and Arthur Marcus Institute for Aging Research and Deanna and Sidney Wolk Center for Memory Health, Hebrew SeniorLife, Boston, MA, USA.
Department of Neurology, Harvard Medical School, Boston, MA, USA.
Guttmann Brain Health Institute, Guttmann Institut, Universitat Autonoma, Barcelona, Spain.

Emiliano Santarnecchi (E)

Berenson-Allen Center for Non-Invasive Brain Stimulation, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Precision Neuroscience & Neuromodulation Program, Massachusetts General Hospital & Harvard Medical School, Boston, MA, USA.

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