TY - JOUR
T1 - Increase in beta frequency phase synchronization and power after a session of high frequency repetitive transcranial magnetic stimulation to the primary motor cortex
AU - De Martino, Enrico
AU - Casali, Adenauer Girardi
AU - Nascimento Couto, Bruno Andry
AU - Graven-Nielsen, Thomas
AU - Ciampi de Andrade, Daniel
N1 - Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.
PY - 2025/1
Y1 - 2025/1
N2 - High-frequency repetitive transcranial magnetic stimulation (rTMS) to the primary motor cortex (M1) is used to treat several neuropsychiatric disorders, but the detailed temporal dynamics of its effects on cortical connectivity remain unclear. Here, we stimulated four cortical targets used for rTMS (M1; dorsolateral-prefrontal cortex, DLPFC; anterior cingulate cortex, ACC; posterosuperior insula, PSI) with TMS coupled with high-density electroencephalography (TMS-EEG) to measure cortical excitability and oscillatory dynamics before and after active- and sham-M1-rTMS. Before and immediately after active or sham M1-rTMS (15 min, 3000 pulses at 10 Hz), single-pulse TMS-evoked EEG was recorded at the four targets in 20 healthy individuals. Cortical excitability and oscillatory measures were extracted at the main frequency bands (α [8–13 Hz], low-β [14–24 Hz], high-β [25–35 Hz]). Active-M1-rTMS increased high-β synchronization in electrodes near the stimulation area and remotely, in the contralateral hemisphere (p = 0.026). Increased high-β synchronization (48–83 ms after TMS-EEG stimulation) was succeeded by enhancement in low-β power (86–144 ms after TMS-EEG stimulation) both locally and in the contralateral hemisphere (p = 0.006). No significant differences were observed in stimulating the DLPFC, ACC, or PSI by TMS-EEG. M1-rTMS engaged a sequence of enhanced phase synchronization, followed by an increase in power occurring within M1, which spread to remote areas and persisted after the end of the stimulation session. These results are relevant to understanding the M1 neuroplastic effects of rTMS in health and may help in the development of informed rTMS therapies in disease.
AB - High-frequency repetitive transcranial magnetic stimulation (rTMS) to the primary motor cortex (M1) is used to treat several neuropsychiatric disorders, but the detailed temporal dynamics of its effects on cortical connectivity remain unclear. Here, we stimulated four cortical targets used for rTMS (M1; dorsolateral-prefrontal cortex, DLPFC; anterior cingulate cortex, ACC; posterosuperior insula, PSI) with TMS coupled with high-density electroencephalography (TMS-EEG) to measure cortical excitability and oscillatory dynamics before and after active- and sham-M1-rTMS. Before and immediately after active or sham M1-rTMS (15 min, 3000 pulses at 10 Hz), single-pulse TMS-evoked EEG was recorded at the four targets in 20 healthy individuals. Cortical excitability and oscillatory measures were extracted at the main frequency bands (α [8–13 Hz], low-β [14–24 Hz], high-β [25–35 Hz]). Active-M1-rTMS increased high-β synchronization in electrodes near the stimulation area and remotely, in the contralateral hemisphere (p = 0.026). Increased high-β synchronization (48–83 ms after TMS-EEG stimulation) was succeeded by enhancement in low-β power (86–144 ms after TMS-EEG stimulation) both locally and in the contralateral hemisphere (p = 0.006). No significant differences were observed in stimulating the DLPFC, ACC, or PSI by TMS-EEG. M1-rTMS engaged a sequence of enhanced phase synchronization, followed by an increase in power occurring within M1, which spread to remote areas and persisted after the end of the stimulation session. These results are relevant to understanding the M1 neuroplastic effects of rTMS in health and may help in the development of informed rTMS therapies in disease.
KW - Transcranial magnetic stimulation
KW - Electroencephalogram
KW - Time-frequency analysis
KW - Phase reset
KW - Primary motor cortex
UR - http://www.scopus.com/inward/record.url?scp=85210016382&partnerID=8YFLogxK
U2 - 10.1016/j.neurot.2024.e00497
DO - 10.1016/j.neurot.2024.e00497
M3 - Journal article
C2 - 39581793
SN - 1878-7479
VL - 22
JO - Neurotherapeutics
JF - Neurotherapeutics
IS - 1
M1 - e00497
ER -