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Structural Connectivity of the Basal Ganglia from Patient-Individual Tractography Is Key for Understanding the Effects of Deep Brain Stimulation in Parkinson's Disease

Title: Structural Connectivity of the Basal Ganglia from Patient-Individual Tractography Is Key for Understanding the Effects of Deep Brain Stimulation in Parkinson's Disease
Authors: Loucao, Ricardo; Kocher, Martin; Brandt, Gregor Alexander; Petry-Schmelzer, Jan Niklas; Barbe, Michael; Dafsari, Haidar; Mana, Josef; Jech, Robert; Wirths, Jochen; Visser-Vandewalle, Veerle; Andrade, Pablo; Baqapuri, Halim; Luehrs, Michael; Linden, David E. J.; Santyr, Brendan; Lozano, Andres; Bongioanni, Alessandro; Jarraya, Bechir; Cukur, Tolga
Source: Loucao, R, Kocher, M, Brandt, G A, Petry-Schmelzer, J N, Barbe, M, Dafsari, H, Mana, J, Jech, R, Wirths, J, Visser-Vandewalle, V, Andrade, P, Baqapuri, H, Luehrs, M, Linden, D E J, Santyr, B, Lozano, A, Bongioanni, A, Jarraya, B, Cukur, T & NEURIPIDES Study Group 2025, 'Structural Connectivity of the Basal Ganglia from Patient-Individual Tractography Is Key for Understanding the Effects of Deep Brain Stimulation in Parkinson's Disease', Stereotactic and Functional Neurosurgery, vol. 103, no. 4, pp. 279-294. https://doi.org/10.1159/000546716
Publication Year: 2025
Collection: Maastricht University Research Publications
Subject Terms: Parkinson's disease; Deep brain stimulation; Tractography; Structural connectivity; SUBTHALAMIC NUCLEUS; DIFFUSION MRI; MOTOR; REGISTRATION; PARCELLATION; ORGANIZATION; SELECTION
Description: Introduction: In Parkinson's disease (PD) patients, modulation of the fibre tracts of the cortico-basal ganglia-thalamo-cortical loop is the presumed mechanism of action of deep brain stimulation (DBS) of the subthalamic nucleus (STN). Therefore, we explored patient-individual cortical structural connectivity of the volume of tissue activated (VTA), as well as DBS-induced modulation of fibre tracts connecting the STN with cortical and subcortical nodes, and their correlation with therapeutic effects. Methods: A retrospective cohort of n = 69 PD patients treated with bilateral DBS of the STN was analysed. Clinical response was assessed from the DBS-induced change in the UPDRS-III motor scores (total and symptom-specific sub-scores) under regular medication after a median follow-up of 9.0 (range 2.6-20.2) months. Tractography based on patient-individual diffusion-weighted MRI was employed in two ways. Whole-brain tractography was used to identify the cortical connections of fibres passing the VTAs, and reconstruction of specific white matter pathways of the motor loop connecting the STN with the basal ganglia and cortex was used to identify the proportion of fibres within these pathways which was modulated by STN-DBS. This proportion of pathway modulation was used in a correlative analysis with clinical outcomes. Results: Fibres traversing the VTAs were primarily connected to the supplementary motor area (SMA) and to a lesser degree to the premotor cortex. Within the pathways connecting the STN with the cortical and subcortical nodes, on average 30-40% (range 10-80%) of the fibres were modulated by STN-DBS. This proportion correlated significantly with the percentage change in UPDRS motor score for fibres connecting the STN with the SMA (ρ = 0.28), pre-SMA (ρ = 0.26), ventral and dorsal premotor cortices (ρ = 0.26 and ρ = 0.29, respectively), and the globus pallidus externus (ρ = 0.26) and internus (ρ = 0.29). Also, good clinical responses for both tremor and rigidity were associated with a significantly (p < ...
Document Type: article in journal/newspaper
Language: English
ISSN: 1011-6125; 1423-0372
Relation: info:eu-repo/semantics/altIdentifier/wos/001554843800001; info:eu-repo/semantics/altIdentifier/pissn/1011-6125; info:eu-repo/semantics/altIdentifier/eissn/1423-0372
DOI: 10.1159/000546716
Availability: https://cris.maastrichtuniversity.nl/en/publications/8579bb7d-4bd3-4195-87b1-1da62a9982c8; https://doi.org/10.1159/000546716
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by-nc/4.0/
Accession Number: edsbas.B2449421
Database: BASE