[18F]F-DOPA Imaging in Patients With Autonomic Failure

Phase

Condition

Parkinson's Disease

Parkinson's With Dementia

Lewy Body Dementia

Treatment

[18F]FDOPA

Entacapone 400mg oral dose

Carbidopa 200mg oral dose

Clinical Study ID

NCT04246437

192021

Ages > 18
All Genders
Accepts Healthy Volunteers

Study Summary

Alpha-synucleinopathies refer to age-related neurodegenerative and dementing disorders, characterized by the accumulation of alpha-synuclein in neurons and/or glia. The anatomical location of alpha-synuclein inclusions (Lewy Bodies) and the pattern of progressive neuronal death (e.g. caudal to rostral brainstem) give rise to distinct neurological phenotypes, including Parkinson's disease (PD), Multiple System Atrophy (MSA), Dementia with Lewy Bodies (DLB). Common to these disorders are the involvement of the central and peripheral autonomic nervous system, where Pure Autonomic Failure (PAF) is thought (a) to be restricted to the peripheral autonomic system, and (b) a clinical risk factor for the development of a central synucleinopathy, and (c) an ideal model to assess biomarkers that predict phenoconversion to PD, MSA, or DLB. Such biomarkers would aid in clinical trial inclusion criteria to ensure assessments of disease- modifying strategies to, delay, or halt, the neurodegenerative process. One of these biomarkers may be related to the neurotransmitter dopamine (DA) and related changes in the substantia nigra (SN) and brainstem. [18F]F-DOPA is a radiolabeled substrate for aromatic amino acid decarboxylase (AAADC), an enzyme involved in the production of dopamine. Use of this radiolabeled substrate in positron emission tomography (PET) may provide insight to changes in monoamine production and how they relate to specific phenoconversions in PAF patients. Overall, this study aims to identify changes in dopamine production in key regions including the SN, locus coeruleus, and brainstem to distinguish between patients with PD, MSA, and DLB, which may provide vital information to predict conversion from peripheral to central nervous system disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patients with a diagnosis if pure autonomic failure
Patients with autonomic failure and possible PD, MSA, or DLB
Healthy adults aged 18 and above
Clinical exam confirming clinical designation

Exclusion

Exclusion Criteria:

Subjects who have any type of bioimplant activated by mechanical, electronic, ormagnetic means (e.g., cochlear implants, pacemakers, neurostimulators,biostimulators, electronic infusion pumps, etc.), because such devices may bedisplaced or malfunction.
Subjects who have any type of ferromagnetic bioimplant that could potentially bedisplaced.
Subjects who have cerebral aneurysm clips.
Subjects who may have shrapnel imbedded in their bodies (such as from war wounds),metal workers and machinists (potential for metallic fragments in or near the eyes).
Subjects who are pregnant, because the effects of high field MRI on fetuses are notyet known.
Minors (younger than 18 years)

Also excluded are subjects incapable of giving informed written consent:

Subjects who cannot adhere to the experimental protocols for any reason, or have aninability to communicate with the researcher.
Subjects who have limited mental ability to give informed consent, mentallyretarded, altered mental status, mental disability, confusion, or psychiatricdisorders.
Prisoners

Study Design