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Granö, I.

Publications and source records attributed to Granö, I..

3 recordsLinked to original sources

Adaptive Bayesian localization of motor representation areas

Transcranial magnetic stimulation (TMS) enables non-invasive localization of cortical motor representations, with important clinical applications in presurgical planning. Existing methods either disregard spatial information about the TMS-induced electric field (E-field) or use acquisition schemes that do not leverage previously elicited motor responses to guide subsequent stimulation. We present an adaptive Bayesian localization method that combines real-time E-field optimization with per-trial probabilistic inference. The cortical origin of the motor responses is represented as a spatial probability distribution that is updated after each stimulus. Subsequent stimuli are then optimized to maximize the expected localization improvement given previous responses. We validated the method experimentally, using multi-locus TMS for adaptive localization and single-coil TMS as a non-adaptive reference with randomized coil placements. Across eight subjects, the adaptive protocol at least halved the number of stimuli required for stable localization compared to the randomized protocol, converging in 60 stimuli on average, with 95% highest-density regions often below 10 mm2 by 150 stimuli.

neuroscience↗

TMS-EEG Indices to Define Local Cortical Excitability Thresholds

IntroductionTranscranial magnetic stimulation (TMS) is widely employed to treat various psychiatric and neurological disorders. However, TMS protocols typically rely on generalizations, particularly in selecting stimulation intensities, leading to suboptimal and variable outcomes. Combining TMS with electroencephalography (EEG) offers a potential solution by allowing direct monitoring of stimulation effects. In this study, we investigate how features of the TMS-EEG signal change with intensity to identify thresholds implying qualitative shifts in the brain response. MethodsWe stimulated eight subjects at both the primary motor cortex (M1) and the pre-supplementary motor area (pre-SMA) with navigated TMS at 15 closely spaced intensities and measured TMS-evoked EEG responses (TMS-evoked potential, TEP) with 60 trials per intensity. TEP thresholds were identified with three methods: by selecting the intensity where the TEP peak-to-peak exceeds 6 V, or by fitting either piecewise-linear or sigmoid curves into the power spectral density (PSD) frequency components to identify nonlinear intensity behavior. ResultsThe identified TEP thresholds varied depending on subject, target, and identification method. In M1, the thresholds attained with the fixed-amplitude and piecewise PSD fit methods averaged around the motor threshold, and in pre-SMA around 120% of the motor threshold. The TEP thresholds yielded by the sigmoid fit method were higher in intensity, and least consistent between subjects. ConclusionsOur findings support the hypothesis that detectable changes in EEG patterns occur at specific TMS intensities. These results provide a basis for individualized stimulation dosing, potentially enhancing therapeutic efficacy and reliability. Future research should focus on refining these methods and validating their clinical applicability across diverse conditions and patient populations.

neuroscience↗

Fast and standardized motor-hotspot determination with automated TMS mapping

Determining the optimal stimulation target for motor responses (motor hotspot) and the required intensity for reliably eliciting said responses (motor threshold) are common procedures in transcranial magnetic stimulation (TMS) research and treatments. However, the procedures for determining them are user-dependent, slow, and lack standardization, leading to long stimulation sessions with potentially inadequate outcomes. Partially automated algorithms for determining the motor threshold have been developed, but the motor hotspot is still largely mapped by hand. Automating the hotspot mapping will accelerate the process and improve standardization and accuracy. We developed a fully automated algorithm for finding the motor hotspot with multi-locus TMS and Bayesian optimization. Tested online in five healthy participants, the algorithm located motor hotspots with (mean {+/-} 95% CI) 2.1 {+/-} 0.7 mm and 6 {+/-} 2{degrees} difference from the global best target with only (mean) 47 stimuli. This is a significant improvement from previous motor-mapping algorithms, which do not optimize for stimulation location and orientation simultaneously. This accurate, fast, and user-independent procedure paves the way for faster experimental processes and more streamlined clinical applications.

neuroscience↗