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PROBE: A Neurophysiology-Informed Bayesian Optimization Framework for Adaptive TMS Motor Hotspot Mapping, Algorithm Design and Monte Carlo Evaluation

Negar NamdariD, Isabella AriasiD, Owen TexteriD, Elisa KallioniemiiD

Abstract

BackgroundAccurate primary motor cortex (M1) hotspot identification is a prerequisite for reliable transcranial magnetic stimulation (TMS) protocols, yet conventional grid search is stimulation-intensive and operator-dependent. Existing Bayesian optimization (BO) implementations, including BOOST and 3D-BOOST, do not model within-session neurophysiological variability. MethodsWe present PROBE (Probabilistic Response-guided Optimization for Brain Exploration), a closed-loop BO framework for three-parameter TMS hotspot mapping over coil position (X, Y) and orientation ({theta}), with five innovations targeting cortical excitability drift, amplitude-dependent noise, transient artifacts, sub-threshold MEP integration (10 {micro}V floor), and cross-subject Gaussian process (GP) prior warm-starting. These were evaluated alone and in combination with amplitude-weighted center-of-gravity (CoG) convergence and estimation across 18 configurations in a Monte Carlo simulation (30 subjects, 3 repetitions each). ResultsAlgorithm configuration significantly affected all outcomes (Friedman tests, all p < 0.001, Kendalls W = 0.50-0.65). MultiFid_CoG_10uV achieved the lowest median XY error (1.14 [0.62-2.12] mm; 50.9 {+/-} 6.2 stimuli; 96.7% convergence), a 68.2% error reduction and 41.5% stimulus reduction relative to grid Search (3.58 [2.66-5.12] mm; 87 stimuli). CoG estimation significantly reduced XY error relative to peak-response selection in 10 of 11 non-CoG configurations (largest gain: MultiFid, 58.7%; adjusted p < 0.001). ConclusionsNeurophysiology-informed BO improved simulated performance under the specified model, extending the 3-DOF approach of Grano et al. (2025) with explicit noise modeling and CoG-based convergence. MultiFid_CoG_10uV and DeltaBO_CoG are selected as candidates for prospective validation in a prospective triple-blind human study.

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