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Projekt Druckansicht

Diffusions-MRT und Resting-state-MRT zur Analyse struktureller und funktioneller Konnektivität sensomotorischer Netzwerke bei fokalen Dystonien

Fachliche Zuordnung Klinische Neurologie; Neurochirurgie und Neuroradiologie
Kognitive und systemische Humanneurowissenschaften
Förderung Förderung von 2014 bis 2017
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 260063645
 
Erstellungsjahr 2018

Zusammenfassung der Projektergebnisse

During the funding period, we performed multimodal MRI studies including resting state and diffusion weighted MRI (DTI) and voxel based morphometry (VBM) in patients with different forms of focal dystonia. These included patients with writer’s cramp (WC), blepharospasm/ Meige syndrome, musicians with embouchure dystonia (ED) and a small group of patients with a newly identified form of genetic dystonia (DYT27). ROI based hypothesis driven and data driven (ICA-) analyses of functional connectivity were performed to study a putative dysfunction of sensorimotor networks already in the absence of dystonic symptoms, i.e. at rest. Voxel wise analyses of local diffusivity as well as probabilistic fiber tracking analyses were applied to study changes of white matter architecture within these subcortical-cortical sensorimotor networks, VBM was additionally performed in patients with WC and ED, both methods revealing a potential anatomical basis for the functional abnormalities. Online recordings of facial surface EMG for the first time allowed the acquisition of resting state data in patients with Blepharospasm/Meige syndrome that are controlled for possible artifacts by involuntary movements at rest. Our resting state studies showed alterations of functional connectivity (FC) especially within sensorimotor networks linking basal-ganglia to primary and secondary sensorimotor cortices as well as for connections of the cerebellum in all these different clinical presentations of focal dystonia. In parallel to these functional findings within basal-ganglia-cortical networks, DTI in patients with WC revealed white matter alterations in connections linking lateral premotor cortices to the basal ganglia, in patients with DYT27 dystonia white matter alterations in cerebello-thalamic and thalamo-cortical connections. Grey matter changes were demonstrated in patients with ED in thalamic and primary sensorimotor/premotor areas in WC within the cerebellum. Further DTI analyses in patients with blepharospasm and ED are still pending. Systematic differences of functional/structural connectivity between action induced (WC, ED) or non-action-induced (Blepharospasm, DYT27) dystonias or between different topographic manifestations (orofacial vs. hand) could not been detected so far. Our findings of changes in FC at rest underlines the importance of cerebello-thalamo-cortical sensorimotor networks in dystonia and may constitute a pathophysiological basis for the emergence of dystonic symptoms, e.g. when interacting with a specific task like writing or playing a musical instrument. In parallel, results of altered white matter architecture and grey matter changes especially in cerebello-thalamic networks and connections between thalamus/basal-ganglia and (pre-)motor cortices may represent a structural pathophysiological basis for these findings of altered FC. Together, these data further contribute to the current theory of focal dystonias as a functional “network” disorder and strengthen the important and longtime underestimated contribution of cerebellar networks.

Projektbezogene Publikationen (Auswahl)

 
 

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