The goal of this prospective open label study is to elucidate the pathophysiology of dystonia and to understand how deep brain stimulation (DBS) influences brain networks. The investigators will enroll patients with dystonia implanted with DBS of the Globus Pallidus internus (GPi) with sensing implantable neurostimulators, capable of measuring GPi local field potentials (LFPs). The main questions it aims to answer are: * does DBS influence pallidal LFPs in the long term? * how the basal-ganglia-thalamo-cortical circuit is modified after DBS? * do LFPs changes correlate with clinical improvement? Participants will undergo to serial clinical evaluations, magnetoencephalography (MEG) and functional Magnetic Resonance Imaging (fMRI) studies. Primarily, the data obtained from our study might help in clarifying basic pathological electrophysiological features of dystonia. These features might be secondarily used in future to provide a framework for an effective application of closed-loop DBS in Dystonia.
Study Type
OBSERVATIONAL
Enrollment
15
fMRI in patients with dystonia implanted with deep brain stimulation with neurostimulators capable of recording local field potentials
EEG-MEG in patients with dystonia implanted with deep brain stimulation with neurostimulators capable of recording local field potentials
registration of local field potential in patients with dystonia implanted with deep brain stimulation
genetic panel for dystonia
Fondazione IRCCS Istituto Neurologico Carlo Besta
Milan, Italy
RECRUITINGLocal field potentials
To confirm the prominent pallidal low frequency oscillations in GPi (LFPs in alpha and theta bands) in dystonic patients and to evaluate the modifications in LFPs after DBS in the long term.
Time frame: 1 year
Coherence LFPs-MEG
To evaluate coherence and/or correlation between GPi acivity and the neural activity in the basal ganglia-thalamo-cortical circuitry. LFPs signals will be co-registered to both EEG/MEG and resting state fMRI.
Time frame: 1 year
Clinical correlations
to find a correlation between modulation of pallidal low-frequency activity and patient's clinical improvement.
Time frame: 1 year
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