Translational modelling of low and medium intensity transcranial magnetic stimulation from rodents to humans

Abstract

AbstractBackgroundRodent models using subthreshold intensities of transcranial magnetic stimulation (TMS) have provided insight into the biological mechanisms of TMS but often differ from human studies in the intensity of the electric field (E-field) induced in the brain.ObjectiveTo develop a finite element method model as a guide for translation between low and medium intensity TMS rodent studies and high intensity TMS studies in humans.MethodsFEM models using three head models (mouse, rat, and human), and eight TMS coils were developed to simulate the magnetic flux density (B-field) and E-field values induced by three intensities.ResultsIn the mouse brain, maximum B-fields ranged from 0.00675 T to 0.936 T and maximum E-field of 0.231 V/m to 60.40 V/m E-field. In the rat brains maximum B-fields ranged from of 0.00696 T to 0.567 T and maximum E-fields of 0.144 V/m to 97.2 V/m. In the human brain, the S90 Standard coil could be used to induce a maximum B-field of 0.643 T and E-field of 241 V/m, while the MC-B70 coil induced 0.564 T B-field and 220 V/m E-field.ConclusionsWe have developed a novel FEM modelling tool that can help guide the replication of rodent studies using low intensity E-fields to human studies using commercial TMS coils. Modelling limitations include lack of data on dielectric values and CSF volumes for rodents and simplification of tissue geometry impacting E-field distribution, methods for mitigating these issues are discussed. A range of additional cross-species factors affecting the translation of E-fields were identified that will aid TMS E-field modelling in both humans and rodents. We present data that describes to what extent translation of brain region-specific E-field values from rodents to humans is possible and detail requirements for future improvement. A graphical abstract of the translational modelling pipeline from this study is provided below (Figure A.1).HighlightsClinical translation of rodent TMS studies is challenging due to the differences in coil and brain size and shape between rodents and humans.We have built a FEM model for the accurate replication of TMS-derived E-fields validated in rodent models in multiple brain regions in humans.This model is useful in designing stimulation parameters for humans based on rodent studies.This model is a critical part of a translational pipeline for evidence based TMS.