Computational Models in Deep Brain Stimulation : Patient‐Specific Simulations, Tractography, and Group Analysis

Deep brain stimulation (DBS) is an established method for symptom relief in movement disorders like Parkinson’s disease, essential tremor (ET), and dystonia. The therapy is based on implanting an electrode with four contacts in the deep brain structures where it provides electrical stimulation, mainly impacting the nerve tracts. Despite the evidence of DBS effectiveness, there are still questions regarding the optimal position of stimulation. With new technology, the possibility to customize the stimulation increases, which makes the programming session for each patient more complicated and tedious. Different computational models have been developed to estimate the anatomical impact of stimulation. Patient‐specific electric field simulations can be used to estimate the spatial extent of the stimulation and superimpose on patient magnetic resonance imaging (MRI) for anatomical analysis. MRI weighted with water diffusion can be used for reconstructions of nerve tracts, a process called tractography. Tractography utilizes the fact that water can move unrestricted along the nerve trajectories, but the diffusion is restricted in the perpendicular direction, i.e., the diffusion is anisotropic. For tremor, the dentato‐rubro‐thalamic tract (DRT) has gained interest. The electric conductivity has corresponding anisotropic characteristics as water diffusion in white brain tissue (nerve tracts). Diffusion MRI can therefore also be used to improve patientspecific simulations by including structure information, i.e., anisotropy. In this thesis, both a workflow for combining patient‐specific simulations with tractography of the DRT and a method for expanding the simulations with anisotropy were developed (Paper I). This was done using four patients with ET. The results show that including anisotropy will impact the simulation result in regions of dense nerve tracts (Paper I‐II). For the tractography, all patients’ estimated stimulation region intersected with the reconstructed DR