About this trial
Parkinson's disease (PD) is the most common degenerative Parkinson's syndrome and is linked, among other things, to the excessive accumulation of an abnormally aggregating protein, alpha-synuclein. Progressive Supranuclear Palsy (PSP) is another Parkinson's syndrome, linked, among other things, to the abnormal accumulation of the protein Tau, and expressed clinically by falls, early cognitive impairment and oculomotor disorders, not present in PD. The onset of these disorders is so gradual that differential diagnosis between the two diseases is only possible at a late stage, on average 3 to 5 years after the onset of symptoms.
To date, there is a lack of validated imaging biomarkers for diagnosing and monitoring PD and PSP. There is therefore an urgent need for the development of robust biomarkers capable of detecting neurodegeneration at an early stage, in order to aid differential diagnosis as soon as symptoms appear, and to potentially enable these patients to be included in specific therapeutic trials (as these diseases are pathophysiologically different) with potential neuroprotective effects.
The development of cutting-edge technologies such as 7T MRI, combined with optimized image processing methods, now enable non-invasive in vivo exploration and analysis of these small structures in terms of ion homeostasis (sodium), microstructure (volumetry, amount of iron and neuromelanin) and connectivity.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients aged between 40 and 80
Fulfilling the diagnostic criteria for MPI (Postuma et al., 2015)
First motor symptom (rigidity, akinesia, tremor) less than 36 months ago
Patient entitled to or affiliated with a social security scheme
Disqualifiers
Patient with a neurological disease of the central nervous system other than those studied (including history of stroke, repeated head trauma, documented encephalitis). In case of doubt, this criterion will be left to the discretion of the principal investigator, who is a neurologist.
Contraindications to 7T MRI: presence of an ocular metallic foreign body (accidental shrapnel or other), pacemaker (cardiac simulator) or neurostimulator (pain treatment), cochlear implants or any implanted electronic medical equipment in general, metallic heart valve, vascular clips implanted on a cranial aneurysm.
Claustrophobia or any other condition preventing full MRI.
Montreal Cognitive Assessment (MOCA) test < 25/30
Trial design
Parallel
Treatments tested in this trial
7 Tesla MRI
Procedure/SurgeryPatients will have a 7T MRI and questionnaires
Treatment groups
Trial outcomes
Primary outcomes
Sodium accumulation between Parkinson disease patients and Progressive Supranuclear Palsy
Comparison of intracerebral sodium accumulation measured by very high-field (7T) cerebral MRI between subjects with Idiopathic Parkinson's Disease and subjects with early-stage Progressive Supra-Nuclear Palsy
Secondary outcomes
Sodium accumulation between Parkinson disease patients (MPI) and control subjects
Comparison of intracerebral sodium accumulation between subjects with early-stage Parkinson's Disease (PD) and control subjects.
Sodium accumulation between Progressive Supra-nuclear patients (soPSP) and control subjects
Comparison of intracerebral sodium accumulation between subjects with soPSP and control subjects.
Brain atrophy between MPI and soPSP patients
3D mapping of brain atrophy differences measured in Voxel Based Morphometry (VBM), value in cm3
Brain atrophy between MPI and control group
3D mapping of brain atrophy differences measured in Voxel Based Morphometry (VBM), value in cm3
Sponsors and contacts
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