A dose-response characterization of transcranial magnetic stimulation intensity and evoked potential amplitude in the dorsolateral prefrontal cortex

• Published in: Scientific reports Vol. 13; no. 1; p. 18650
• Main Authors: Krile, Louisa, Ensafi, Elnaz, Cole, Jaeden, Noor, Mah, Protzner, Andrea B., McGirr, Alexander
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 30-10-2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/378; 631/443; Dose-response effects; EEG; Humanities and Social Sciences; Magnetic fields; multidisciplinary; Plasticity; Prefrontal cortex; Science; Science (multidisciplinary); Transcranial magnetic stimulation
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-45730-y

By combining transcranial magnetic stimulation (TMS) with electroencephalography, human cortical circuits can be directly interrogated. The resulting electrical trace contains TMS-evoked potential (TEP) components, and it is not known whether the amplitudes of these components are stimulus intensity dependent. We examined this in the left dorsolateral prefrontal cortex in nineteen healthy adult participants and extracted TEP amplitudes for the N40, P60, N120, and P200 components at 110%, 120%, and 130% of resting motor threshold (RMT). To probe plasticity of putative stimulus intensity dose-response relationships, this was repeated after participants received intermittent theta burst stimulation (iTBS; 600 pulses, 80% RMT). The amplitude of the N120 and P200 components exhibited a stimulus intensity dose-response relationship, however the N40 and P60 components did not. After iTBS, the N40 and P60 components continued to exhibit a lack of stimulus intensity dose-dependency, and the P200 dose-response was unchanged. In the N120 component, however, we saw evidence of change within the stimulus intensity dose-dependent relationship characterized by a decrease in absolute peak amplitudes at lower stimulus intensities. These data suggest that TEP components have heterogeneous dose-response relationships, with implications for standardizing and harmonizing methods across experiments. Moreover, the selective modification of the N120 dose-response relationship may provide a novel marker for iTBS plasticity in health and disease.