Poster No:
51
Submission Type:
Abstract Submission
Authors:
Evgenii Kim1,2, Mohammad Daneshzand1,2, Sergey Makarov3, Konstantin Weise4,5, Ole Numssen4, Thomas Knösche4, Dylan Edwards6,7, Tommy Raij1,2, Aapo Nummenmaa1,2
Institutions:
1Massachusetts General Hospital, Boston, MA, 2Harvard Medical School, Boston, MA, 3Worcester Polytechnic Institute, Boston, MA, 4Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Saxony, 5Leipzig University of Applied Sciences, Leipzig, Germany, 6Thomas Jefferson University, Philadelphia, PA, 7Moss Rehabilitation Research Institute, Philadelphia, PA
First Author:
Evgenii Kim
Massachusetts General Hospital|Harvard Medical School
Boston, MA|Boston, MA
Co-Author(s):
Mohammad Daneshzand
Massachusetts General Hospital|Harvard Medical School
Boston, MA|Boston, MA
Konstantin Weise
Max Planck Institute for Human Cognitive and Brain Sciences|Leipzig University of Applied Sciences
Leipzig, Saxony|Leipzig, Germany
Ole Numssen
Max Planck Institute for Human Cognitive and Brain Sciences
Leipzig, Saxony
Thomas Knösche
Max Planck Institute for Human Cognitive and Brain Sciences
Leipzig, Saxony
Dylan Edwards
Thomas Jefferson University|Moss Rehabilitation Research Institute
Philadelphia, PA|Philadelphia, PA
Tommy Raij
Massachusetts General Hospital|Harvard Medical School
Boston, MA|Boston, MA
Aapo Nummenmaa
Massachusetts General Hospital|Harvard Medical School
Boston, MA|Boston, MA
Introduction:
Transcranial Magnetic Stimulation (TMS) is a powerful non-invasive neurostimulation method that is established in preoperative functional mapping for neurosurgical interventions[1]. The geometry of the coil plays a crucial role in shaping the induced electric field (E-field), thus influencing the spatial specificity and efficacy of TMS pulses (larger coils provide enhanced depth penetration but with a trade-off of decreased focality)[2]. The spatial extent of the E-field determined by the coil type has been a crucial consideration for improved quantitative TMS protocols, where the goal is to isolate a cortical "hotspot" for a target muscle[3]. Yet, it is not well-characterized how invariant the mapping results are with respect to the size of the TMS coil, and/or if using different coils would provide complementary information.
Methods:
Data were acquired from a single healthy, right-handed male subject who provided written informed consent. The workflow is illustrated in Fig. 1. Before TMS session, T1- and T2-weighted MR images were obtained using a Siemens 3 Tesla scanner. The head model was created from MRI using the SimNIBS headreco[4]. TMS pulses were delivered using a MagPro X100 stimulator (MagVenture, Denmark). Two figure-of-eight coils, B60 and B35 (MagVenture; with coil diameter 2x75 mm and 2x46 mm, respectively) were used in separate runs during the same session. Each run involved 250 TMS single biphasic pulses at 5-second intervals. The stimulation intensity for B60 was set at 150% of the resting motor threshold (rMT), which corresponds to 68% of the maximum stimulator output (MSO). Meanwhile, B35 was operated at 133% of the rMT (limited by 100% MSO). For each stimulation, each coil was randomly positioned around the motor cortex. Coil locations were recorded using a neuronavigation system (TMS Navigator, Localite, Germany). Motor evoked potentials (MEPs) were recorded from three finger muscles - first dorsal interosseous (FDI), abductor digiti minimi (ADM), and abductor pollicis brevis (APB). MEPs were sampled at 5 kHz and post-processed with a bandpass filter (100-1000 Hz). Coil positions and the head model were utilized to compute the E-fields using an LU-based BEM-FMM[5]. The identification of the "hotspot" for each muscle was determined by maximum R2 scores derived from logarithmic sigmoid regression, establishing the correspondence between induced magnitude E-field distribution and MEPs[6].

Results:
A goodness-of-fit map illustrating the functional cortical representation of the fingers under two coils is presented in Fig. 2. The functional map was further derived by combining B60 and B35 datasets. To ensure an equivalent number of data points, 125 random trials were selected from the B60 coil and 125 from the B35 coil. The identified "hotspots" were consistently within a 3 mm range across three coil configurations (B60, B35, combined) for each muscle. As expected, the B35 coil with higher focality of E-field exhibited an improved localization in the goodness-of-fit map. Specifically, the B60 mapping showed a "spread" of the hot spot neighboring gyri (Fig. 2, red arrows) that is likely associated with the limitations of the TMS coil focality, rather than the actual extent of the cortical motor representation. The results from the combination of two coil types produced a functional map that captures the "best of both worlds" – the spatial spread to the neighboring gyri of the B60 coil is reduced, while the R2 scores of the B35 are enhanced.

Conclusions:
Our study showed that TMS mapping results across two coils of different sizes produced qualitatively similar outcomes, indicating the overall robustness of the approach. Combining both coil types produced a balanced mixture of both features in terms of sensitivity and specificity. In the future, by utilizing multichannel TMS coil arrays[7], we may generate a wider range of E-field patterns and further reduce the ambiguity in the localization maps.
Brain Stimulation:
Non-invasive Magnetic/TMS 1
TMS 2
Keywords:
Cortex
Transcranial Magnetic Stimulation (TMS)
Other - Functional mapping
1|2Indicates the priority used for review
Provide references using author date format
[1] Raffa, G. (2019), "The role of navigated transcranial magnetic stimulation for surgery of motor-eloquent brain tumors: a systematic review and meta-analysis," Clinical Neurology Neurosurgery, 180, 7-17.
[2] Drakaki, M. (2022), "Database of 25 validated coil models for electric field simulations for TMS," Brain Stimulation, 15(3), 697-706.
[3] Numssen, O. (2021), "Efficient high-resolution TMS mapping of the human motor cortex by nonlinear regression," Neuroimage, 245, 118654.
[4] Saturnino, G.B. (2019), "SimNIBS 2.1: A Comprehensive Pipeline for Individualized Electric Field Modelling for Transcranial Brain Stimulation," Brain and Human Body Modeling: Computational Human Modeling at EMBC 2018, Chapter 1.
[5] Makaroff, S.N. (2023), "A fast direct solver for surface-based whole-head modeling of transcranial magnetic stimulation," Scientific Reports, 13(1), 18657.
[6] Weise, K. (2023), "Precise motor mapping with transcranial magnetic stimulation," Nature Protocol, 18(2), 293-318.
[7] Navarro de Lara, L.I. (2021), "A 3-axis coil design for multichannel TMS arrays," Neuroimage, 224, 117355.