Rapid assessment of regional cerebral metabolic abnormalities in single subjects with quantitative and nonquantitative [18F]FDG PET:: A clinical validation of statistical parametric mapping

被引:233
作者
Signorini, M
Paulesu, E
Friston, K
Perani, D
Colleluori, A
Lucignani, G
Grassi, F
Bettinardi, V
Frackowiak, RSJ
Fazio, F
机构
[1] Univ Milan, Ist Sci H San Raffaele, CNR, INB, I-20132 Milan, Italy
[2] Inst Neurol, Funct Imaging Lab, Wellcome Dept Cognit Neurol, London WC1N 3BG, England
基金
英国惠康基金;
关键词
positron emission tomography; statistical parametric mapping; single-case studies; dementia; specific language impairment; multiple sclerosis; epilepsy;
D O I
10.1006/nimg.1998.0381
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The [F-18]fluorodeoxyglucose ([F-18]FDG) method for measuring brain metabolism has not the wide clinical application that one might expect, partly because of its high cost and the complexity of the quantification procedure, but also because of reporting techniques based on region of interest (ROI) analysis, which are time-consuming and not fully objective. In this paper we report a clinical validation of statistical parametric mapping (SPM) using rCMRglc (quantitative) and radioactivity distribution (nonquantitative) [F-18]FDG PET data. We show that a 10-min noninteractive voxel-based SPM analysis on a standard workstation enables objective assessment, including localization in stereotactic space, of regional glucose consumption abnormalities, whose reliability can be assessed on statistical and clinical grounds, Clinical validity was established using a small series of patients with degenerative or developmental disorders, including probable Alzheimer's disease, progressive aphasia, multiple sclerosis, developmental specific language impairment, and epilepsy. Analysis of quantitative and nonquantitative data showed the same pattern of results, suggesting that, for clinical purposes, quantitation and invasive arterial cannulation can be avoided. This should facilitate a wider application of the technique and the extension of SPM clinical analysis to (H2O)-O-15 PET or high resolution SPECT perfusion studies. (C) 1999 Academic Press.
引用
收藏
页码:63 / 80
页数:18
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