Vingerhoets F J, Schulzer M, Ruth T J, Holden J E, Snow B J
Neurodegenerative Disorders Centre, University of British Columbia, Vancouver, Canada.
J Nucl Med. 1996 Mar;37(3):421-6.
Fluorine-18-fluorodopa (F-Dopa) PET assesses the integrity of the nigrostriatal dopaminergic neurons in Parkinson's disease. It has been used in longitudinal studies to measure the progression of Parkinson's disease and the effects of medications and intracerebral transplants. The significance of changes in PET indices in such studies depends largely on the reproducibility of the F-Dopa PET measurements.
We performed repeated F-Dopa PET scans in 12 subjects with Parkinson's disease (between Hoehn and Yahr stages I and III) to measure scan-to-scan variations. Data were analyzed using five methods comprising two sets of regions of interest (ROIs) (total striatum and substriatal), the striatum-to-cortex ratio and two graphical methods (one using plasma radioactivity, the other using cortical radioactivity as the input function). We also studied the effectiveness of each method in discriminating between patients with Parkinson's disease and normal subjects using data obtained from a similar study in 10 normal subjects.
We found reliability coefficients between 66% and 93%; the scan-to-scan intrasubject standard deviation ranged from 2% to 16% of the mean value depending on the method of analysis and the size of the ROIs. All methods discriminated significantly between patients with Parkinson's disease and normal subjects. The ability to discriminate, as reflected by the intergroup/intragroup ratio of variance, ranged from 2 to 18.
These results permit selection of the best method of analysis for studies of nigrostriatal dopaminergic function.
氟-18-氟多巴(F-Dopa)正电子发射断层扫描(PET)用于评估帕金森病中黑质纹状体多巴胺能神经元的完整性。它已被用于纵向研究,以测量帕金森病的进展以及药物和脑内移植的效果。在此类研究中,PET指标变化的意义在很大程度上取决于F-Dopa PET测量的可重复性。
我们对12例帕金森病患者(霍恩和雅尔分期为I期和III期之间)进行了重复的F-Dopa PET扫描,以测量扫描间的差异。使用五种方法分析数据,这五种方法包括两组感兴趣区域(ROI)(整个纹状体和纹状体下区域)、纹状体与皮质的比值以及两种图像分析方法(一种使用血浆放射性,另一种使用皮质放射性作为输入函数)。我们还使用从10名正常受试者的类似研究中获得的数据,研究了每种方法在区分帕金森病患者和正常受试者方面的有效性。
我们发现可靠性系数在66%至93%之间;根据分析方法和ROI大小,扫描间受试者内标准差范围为平均值的2%至16%。所有方法在帕金森病患者和正常受试者之间均有显著差异。以组间/组内方差比反映的区分能力范围为2至18。
这些结果有助于为黑质纹状体多巴胺能功能研究选择最佳分析方法。