Herholz K
Neurologische Universitätsklinik und Max-Planck-Institut für neurologische Forschung, Cologne, Germany.
Alzheimer Dis Assoc Disord. 1995 Spring;9(1):6-16. doi: 10.1097/00002093-199505000-00004.
Positron emission tomography (PET) with 18F-2-fluoro-2-deoxy-D-glucose (FDG) demonstrates a typical pattern of impairment of regional metabolic rates of glucose (rCMRGlu) in most patients with a clinical diagnosis of probable Alzheimer's disease (AD): reduction of rCMRGlu in temporo-parietal association cortex, more variably also in prefontal cortex, but relative preservation of primary visual and sensoriomotor cortex, striatum, and cerebellum. Apart from early stages, both hemispheres are affected, but pronounced asymmetries may be present. With the exception of Parkinson's disease with dementia, the complete pattern is rarely seen in other dementing conditions, which usually lead to more global, frontal or multifocal metabolic impairment. Severity of dementia is mainly correlated with temporo-parietal rCMRGlu reduction, probably irrespective of the cause of dementia, and the neuropsychological profile is related to the asymmetry of metabolic alterations. Procedures are available for assessment of the typical pattern that yield comparable results in different laboratories, and have a high accuracy for discrimination between normals and probable AD. Diagnostic accuracy is better for presenile than for senile dementia of Alzheimer type, and for moderate to severe cases than for mild dementia. A definitive judgment of the diagnostic value of FDG PET in AD is hindered by the lack of sufficient data with diagnosis confirmed at autopsy.
使用18F-2-氟-2-脱氧-D-葡萄糖(FDG)的正电子发射断层扫描(PET)显示,大多数临床诊断为可能的阿尔茨海默病(AD)的患者存在典型的局部葡萄糖代谢率(rCMRGlu)受损模式:颞顶叶联合皮质的rCMRGlu降低,前额叶皮质也有不同程度的降低,但初级视觉和感觉运动皮质、纹状体及小脑相对保留。除早期阶段外,双侧半球均受影响,但可能存在明显的不对称性。除帕金森病伴痴呆外,其他痴呆性疾病很少出现这种完整模式,通常会导致更广泛、额叶或多灶性代谢损害。痴呆的严重程度主要与颞顶叶rCMRGlu降低相关,可能与痴呆病因无关,神经心理学特征与代谢改变的不对称性有关。现有评估典型模式的方法,在不同实验室能得出可比结果,对区分正常人和可能的AD具有较高准确性。早老性阿尔茨海默型痴呆的诊断准确性优于老年性痴呆,中重度病例优于轻度痴呆。由于缺乏尸检确诊的充分数据,FDG PET在AD中的诊断价值难以做出明确判断。