The Distribution and Quantification of Specific Binding of the Positron Emission Tomography Tracer R)-[11C]PK11195 in Normal Human Subjects
试验速览
- 阶段
- 1 期
- 发起方
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- specific binding of tracer depending on age
研究概览
简要总结
This is a study using Positron Emission Tomography (PET) to study the normal distribution of the PET ligand (R)-[11C]PK11195. This ligand will be used to study inflammation in the brain in several brain disorders like Alzheimer's disease and traumatic brain injury.
详细描述
At the University Hospital Vrije Universiteit the PET ligand PK11195 labeled with carbon-11, (R)-[11C]PK11195, will be used to study microglia activation in-vivo in patients with traumatic brain damage, Alzheimer disease, multiple sclerosis and neuritis optica, disorders with unknown pathophysiology and treatment difficulties.
PK11195 (1-(2-chlorophenyl)-N-methyl-N-1(1-methylpropyl)-3 isoquinolinecarboxamide) is a highly specific ligand for the peripheral benzodiazepine-binding site, which is particularly abundant on cells of the mononuclear macrophage line (Myers et al., 1991). In normal human brain, the peripheral-type benzodiazepine receptor ligand PK11195 exhibits low to minimal binding primarily associated with the choroid plexus, ependymal linings and glial cells. However, following neuronal damage, the cells involved in the ensuing gliosis, microglia, show a marked increase in expression of these sites (Stephenson et al., 1995;Conway et al., 1998).
PK11195 labeled with carbon-11 is a PET ligand to peripheral type benzodiazepine receptors which has already been used in patients with stroke (Ramsay et al., 1992), Rasmussen's encephalitis (Banati et al., 1999), multiple sclerosis (Banati et al., 1997) and facial nerve lesions (Myers et al., 1999). However, no tracer kinetic model for quantification has been fully validated for(R)-[11C]PK11195. In order to use (R)-[11C]PK11195 for PET-imaging of microglia activation and to use it in the longitudinal monitoring of disease progression, baseline levels of ligand uptake in a healthy control population are required. This study aims to measure (R)-[11C]PK11195 uptake in normal brain in different age groups and to develop methods for quantification of specific binding of (R)-[11C]PK11195. Because (R)-[11C]PK11195 uptake depends on regional bloodflow, each (R)-[11C]PK11195 scan will be preceded by a cerebral bloodflow scan with H215O.
OBJECTIVES
- Determine the distribution of (R)-[11C]PK11195 in normal brain
- Develop methods for quantification of specific binding of (R)-[11C]PK11195
- Determine the metabolic profile of (R)-[11C]PK11195 in healthy volunteers
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male and female subjects
- •Good physical and mental Health which will be evaluated with medical history, a physical examination and screening laboratory tests (see appendix 1).
- •Age between 18 and 40 years (20 subjects) and between 40 and 80 years (20 subjects).
- •Mini Mental State score >27
- •Body Mass Index (B.M.I.) between 20 -
- •Written informed consent of the subject.
- •Hb must be >8 mmol \ liter at the time of the screening.
排除标准
- •Previous neurotrauma with loss of consciousness
- •Any clinical significant abnormality of any clinical laboratory test, including drug screening, or ECG abnormality.
- •History of hypertension
- •Any subject who has received any investigational medication within 30 days prior to the start of this study, or who is scheduled to receive an investigational drug.
- •History of psychiatric or neurological illness
- •History of psychiatric or neurological illness in first-degree relatives
- •History of alcohol and/or drug abuse (DSM-IV criteria)
- •Current use of any medication
- •Blood donation within 3 months before the scan day
- •Claustrophobia
- •Metal objects in or around the body (braces, pacemaker, metal fragments);
结局指标
主要结局
specific binding of tracer depending on age
次要结局
- tracer kinetic method