Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, CA, USA.
Alzheimers Dement. 2010 May;6(3):221-9. doi: 10.1016/j.jalz.2010.03.003.
This is a progress report of the Alzheimer's Disease Neuroimaging Initiative (ADNI) positron emission tomography (PET) Core.
The Core has supervised the acquisition, quality control, and analysis of longitudinal [(18)F]fluorodeoxyglucose PET (FDG-PET) data in approximately half of the ADNI cohort. In an "add on" study, approximately 100 subjects also underwent scanning with [(11)C] Pittsburgh compound B PET for amyloid imaging. The Core developed quality control procedures and standardized image acquisition by developing an imaging protocol that has been widely adopted in academic and pharmaceutical industry studies. Data processing provides users with scans that have identical orientation and resolution characteristics despite acquisition on multiple scanner models. The Core labs have used many different approaches to characterize differences between subject groups (Alzheimer's disease, mild cognitive impairment, controls), to examine longitudinal change over time in glucose metabolism and amyloid deposition, and to assess the use of FDG-PET as a potential outcome measure in clinical trials.
ADNI data indicate that FDG-PET increases statistical power over traditional cognitive measures, might aid subject selection, and could substantially reduce the sample size in a clinical trial. Pittsburgh compound B PET data showed expected group differences, and identified subjects with significant annual increases in amyloid load across the subject groups. The next activities of the PET core in ADNI will entail developing standardized protocols for amyloid imaging using the [(18)F]-labeled amyloid imaging agent AV45, which can be delivered to virtually all ADNI sites.
ADNI has demonstrated the feasibility and utility of multicenter PET studies and is helping to clarify the role of biomarkers in the study of aging and dementia.
这是阿尔茨海默病神经影像学倡议 (ADNI) 正电子发射断层扫描 (PET) 核心的进展报告。
该核心监督了大约一半 ADNI 队列的纵向 [(18)F] 氟脱氧葡萄糖 PET (FDG-PET) 数据的获取、质量控制和分析。在一项“附加”研究中,大约 100 名受试者还接受了 [(11)C] 匹兹堡化合物 B PET 扫描以进行淀粉样蛋白成像。该核心通过开发一种已广泛应用于学术和制药行业研究的成像协议,制定了质量控制程序并标准化了图像采集。数据处理为用户提供了具有相同方向和分辨率特征的扫描,尽管是在多个扫描仪模型上采集的。核心实验室使用了许多不同的方法来描述受试者组(阿尔茨海默病、轻度认知障碍、对照组)之间的差异,检查葡萄糖代谢和淀粉样蛋白沉积随时间的纵向变化,并评估 FDG-PET 作为临床试验中的潜在结果测量。
ADNI 数据表明,FDG-PET 比传统认知测量具有更高的统计功效,可能有助于受试者选择,并可大大减少临床试验中的样本量。匹兹堡化合物 B PET 数据显示了预期的组间差异,并确定了在整个受试者组中淀粉样蛋白负荷呈显著年度增加的受试者。ADNI 中 PET 核心的下一个活动将涉及制定使用 [(18)F] 标记的淀粉样蛋白成像剂 AV45 进行淀粉样蛋白成像的标准化协议,该协议几乎可以提供给所有 ADNI 站点。
ADNI 已经证明了多中心 PET 研究的可行性和实用性,并有助于阐明生物标志物在衰老和痴呆研究中的作用。