Contribution of the Cerebellum In Sensory-motor Adaptation Via Gamma Oscillations: the Case of Dystonia

Not Applicable

Completed

• Conditions: Primary Dystonia
• Interventions: Other: active cerebellar stimulation; Other: sham cerebellar stimulation

• Registration Number: NCT02073630
• Lead Sponsor: Institut National de la Santé Et de la Recherche Médicale, France

Brief Summary

Dystonia, a disabling disease with uncontrolled movement disorders was considered to be a manifestation of basal ganglia dysfunction, yet there is accumulating evidence from animal and human experiments that the cerebellum plays a prominent role in the pathophysiology of dystonia. Our recent results suggest a deficient cerebellar sensory encoding in dystonia, resulting in a decoupling of the motor component from the afferent information flow resulting from changes in the environment. An overall loss of gabaergic-mediated inhibition is at the forefront in dynamic changes in neural circuitry described in dystonia. In the mature brain gabaergic control the generation of temporal synchronies and oscillations in the glutamatergic neurons. Taken these all together with the results of a pilot experiment, the investigators hypothesize that deficient synchronies in the fast gamma range are one of the key mechanisms leading to abnormal communication inside the cerebello-cortical network in dystonia. The investigators aim first to demonstrate it by means of MEG (Magneto encepholography) recordings allowing to reconstruct the spatio-temporal dynamics of gamma oscillations in the nodes of the cerebello-cortical network. The investigators then aim to re-establish (if lost) or boost (if decreased) the defective synchronies by applying to the cerebellum at high gamma frequency a non invasive transcranial alternative current stimulation.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-02
• Study First Submitted: 2014-02-19
• Study First Submitted QC: 2014-02-25
• Study First Posted: 2014-02-27
• Primary Completion: 2016-02
• Status Verified: 2016-08
• Study Completion: 2016-08
• Last Update Submitted: 2017-10-31
• Last Update Posted: 2017-11-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 63

Inclusion Criteria

• primary upper limb dystonia
• normal physical and neurological examination except for dystonia
• no treatment with botulinum toxin during the three months preceding the study

Exclusion Criteria

• Writing tremor
• current neurological or psychiatric illness other than dystonia
• uncontrollable medical problems not related to dystonia
• pregnancy, breast feeding women and women who are of childbearing age and not practicing adequate birth control

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Healthy subjects	active cerebellar stimulation	healthy subjects will receive either sham or active cerebellar stimulation
Healthy subjects	sham cerebellar stimulation	healthy subjects will receive either sham or active cerebellar stimulation
Dystonia	sham cerebellar stimulation	dystonic patients will receive either sham or active cerebellar stimulation
Dystonia	active cerebellar stimulation	dystonic patients will receive either sham or active cerebellar stimulation

Primary Outcome Measures

Name	Time	Method
change in gamma oscillations power in the cerebellum during a sensorimotor adaptation task	measures will be done at each of 3 visits: visit1, visit2 at expected average 7 days after visit1 and visit3 at expected average 14 days after visit1	MEG recording will be performed using a whole-head 306-channels MEG system (Elekta Neuromag® TriuxTM System) comprising 204 planar gradiometers and 102 magnetometers regularly distributed at 102 locations over the scalp. MEG data will be coregistered with the structural MRI of each subject using BrainStorm (http://neuroimage.usc.edu/brainstorm).; The localization of the source will be constrained with the individual anatomy obtained with MRI.

Secondary Outcome Measures

Name	Time	Method
synchrony in the gamma band between the cerebellum and the sensorimotor cortex	measures will be done at each of 3 visits: visit1, visit2 at expected average 7 days after visit1 and visit3 at expected average 14 days after visit1	We will also conduct a functional connectivity analysis to assess the neuronal interactions between the cerebellum and the thalamus, the thalamus and the motor cortex by quantifying correlations between power envelopes. We will compute Pearson's linear correlation between the power envelopes from two different locations (between couples of magnetometers and couples of nodes at the source level).

Trial Locations

Locations (1)

ICM GH Pitié Salpetrière; 🇫🇷 Paris, France