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Preconditioning Stimulus Intensity Alters Paired-Pulse TMS Evoked Potentials
Vishal Rawji1, Isabella Kaczmarczyk1, Lorenzo Rocchi1,2
1Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Paired-pulse transcranial magnetic stimulation (ppTMS) combined with electroencephalography (EEG) measures cortical function. Lower preconditioning stimulus intensities better distinguish intracortical inhibition using TMS-EEG.
Area of Science:
- Neuroscience
- Neurophysiology
- Brain Stimulation
Background:
- Motor cortex (M1) paired-pulse transcranial magnetic stimulation (ppTMS) using motor-evoked potentials (MEPs) assesses intracortical dynamics.
- MEPs confound cortical and spinal excitability, limiting precise cortical function assessment.
- Concurrent TMS-EEG offers a peripheral confound-free measure of cortical function via TMS-evoked potentials (TEPs).
Purpose of the Study:
- To investigate the effect of varying preconditioning stimulus intensities in ppTMS on TEPs.
- To compare the sensitivity of TEPs versus MEPs to intracortical inhibition across different stimulus intensities.
Main Methods:
- Single-pulse and ppTMS paradigms were applied to the left M1.
- Three ppTMS conditions used preconditioning stimulus intensities of 70%, 80%, and 90% of resting motor threshold.
- Motor-evoked potentials (MEPs) and TMS-evoked potentials (TEPs) were recorded concurrently.
Main Results:
- Corticospinal inhibition was observed across all ppTMS conditions.
- ppTMS reduced TEP peaks primarily at 70% intensity, with less reduction at 80% and no reduction at 90%.
- A significant negative correlation was found between MEPs and the N45 TEP peak, particularly at lower intensities.
Conclusions:
- Unlike MEPs, ppTMS TEPs do not show inhibition across all tested intensities.
- TEP responses to M1 ppTMS are intensity-dependent, with lower intensities yielding better discriminability.
- Minimizing preconditioning stimulus intensity is recommended for ppTMS-EEG studies probing intracortical inhibition.
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