The University of Manchester, Wolfson Molecular Imaging Centre, 27 Palatine Road, Manchester, UK.
Biomark Med. 2012 Aug;6(4):431-9. doi: 10.2217/bmm.12.51.
PET with the glucose analog FDG as a tracer is a mature and increasingly available clinical imaging technique that can improve the diagnostic accuracy for Alzheimer's disease, which is of particular value at an early stage of the disease when clinical symptoms are still mild and nonspecific. It can also monitor progression of Alzheimer's disease, and the findings are closely related to clinical symptoms. FDG PET, therefore, could also potentially be used as an imaging biomarker for selection of patients and assessment of outcome in clinical trials. Several published intervention studies indicate a good correspondence between clinical outcome and FDG PET findings, but study designs and methods used for data analysis vary widely. Recent developments towards standardization of largely user-independent methods for quantification of regional metabolic impairment on FDG PET scans will allow a new generation of studies that could provide the required evidence for full qualification of FDG PET as an imaging biomarker in clinical trials.
正电子发射断层扫描(PET)采用葡萄糖类似物 FDG 作为示踪剂,是一种成熟且日益普及的临床影像技术,可提高阿尔茨海默病的诊断准确性,在疾病的早期阶段尤其有价值,此时临床症状仍较为轻微且不具特异性。它还可监测阿尔茨海默病的进展,其结果与临床症状密切相关。因此,FDG PET 也有可能作为一种影像生物标志物,用于选择患者和评估临床试验的结果。几项已发表的干预研究表明,FDG PET 发现与临床结果之间存在良好的对应关系,但用于数据分析的研究设计和方法差异很大。目前,针对 FDG PET 扫描中区域性代谢损伤的定量分析,已朝着广泛应用、用户独立性强的方法标准化方向发展,这将有助于开展新一代的研究,为充分证明 FDG PET 作为临床试验影像生物标志物的资格提供所需的证据。