[18F]F-DOPA Imaging in Patients With Autonomic Failure
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Differences in FDOPA uptake across patient populations
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •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
排除标准
- •Subjects who have any type of bioimplant activated by mechanical, electronic, or magnetic means (e.g., cochlear implants, pacemakers, neurostimulators, biostimulators, electronic infusion pumps, etc.), because such devices may be displaced or malfunction.
- •Subjects who have any type of ferromagnetic bioimplant that could potentially be displaced.
- •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 not yet 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 an inability to communicate with the researcher.
- •Subjects who have limited mental ability to give informed consent, mentally retarded, altered mental status, mental disability, confusion, or psychiatric disorders.
- •Prisoners
研究组 & 干预措施
[18F]F-DOPA
All patients will receive [18F]F-DOPA for PET imaging to measure pre-synaptic dopamine in the brain.
干预措施: [18F]FDOPA (Drug)
[18F]F-DOPA
All patients will receive [18F]F-DOPA for PET imaging to measure pre-synaptic dopamine in the brain.
干预措施: Carbidopa 200mg oral dose (Drug)
[18F]F-DOPA
All patients will receive [18F]F-DOPA for PET imaging to measure pre-synaptic dopamine in the brain.
干预措施: Entacapone 400mg oral dose (Drug)
结局指标
主要结局
Differences in FDOPA uptake across patient populations
时间窗: 95 minutes post-PET after start of PET imaging
Specific FDOPA uptake, Ki, will be calculated via a reference Logan plot to provide voxelwise measurements of FDOPA uptake. Mean uptake will be assessed in brain regions-of-interest in 40 participants to assess potential differences across different autonomic failure-related diseases.
次要结局
未报告次要终点
研究者
Daniel Claassen
Professor of Neurology
Vanderbilt University Medical Center