Kim E J, Cho S S, Jeong Y, Park K C, Kang S J, Kang E, Kim S E, Lee K H, Na D L
Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-dong, Kangnam-gu, Seoul 135-710, Korea.
Brain. 2005 Aug;128(Pt 8):1790-801. doi: 10.1093/brain/awh539. Epub 2005 May 11.
The aims of this cross-sectional study were (i) to compare the overall glucose metabolism between early onset and late onset Alzheimer's disease in a large sample of patients; and (ii) to investigate the pattern of glucose metabolism as a function of dementia severity in early onset versus late onset Alzheimer's disease, using a statistical parametric mapping (SPM) analysis. Subjects consisted of four groups: 74 patients with early onset Alzheimer's disease, 46 patients with late onset of the disease, and two control groups age matched to each patient group. All the subjects underwent 2-[(18)F]fluoro-2-deoxy-d-glucose (FDG)-PET under the same scanning conditions. Severity of dementia was rated with the Clincial Dementia Rating (CDR). Voxel-based SPM99 was used for statistical analyses. Overall glucose hypometabolism of early onset Alzheimer's disease patients was much greater in magnitude and extent than that of late onset patients, though both groups were similar in dementia severity: the early onset group showed more severe hypometabolism in parietal, frontal and subcortical (basal ganglia and thalamus) areas. When the decline of glucose metabolism was compared as a function of CDR stage, the slope was steeper in early onset than in late onset Alzheimer's disease. The rapid decline occurred at CDR 0.5-1 in the early onset group, whereas similar changes occurred at CDR 2-3 in the late onset group. The greater hypometabolism in early onset than in late onset patients is required to reach the same severity of dementia, probably reflecting greater functional reserve in younger than in older subjects. Alternatively, the metabolic decline curve suggests that the early onset patients may take a more rapid course in the reduction of glucose metabolism than the late onset patients.
(i)在大量患者样本中比较早发型和晚发型阿尔茨海默病患者的整体葡萄糖代谢情况;(ii)使用统计参数映射(SPM)分析,研究早发型与晚发型阿尔茨海默病患者中葡萄糖代谢模式随痴呆严重程度的变化情况。研究对象包括四组:74例早发型阿尔茨海默病患者、46例晚发型阿尔茨海默病患者以及与每组患者年龄匹配的两个对照组。所有受试者均在相同扫描条件下接受2-[(18)F]氟-2-脱氧-D-葡萄糖(FDG)-PET检查。使用临床痴呆评定量表(CDR)对痴呆严重程度进行评分。基于体素的SPM99用于统计分析。早发型阿尔茨海默病患者的整体葡萄糖代谢减退在程度和范围上均比晚发型患者严重得多,尽管两组在痴呆严重程度方面相似:早发型组在顶叶、额叶和皮质下(基底神经节和丘脑)区域表现出更严重的代谢减退。当将葡萄糖代谢下降情况作为CDR阶段的函数进行比较时,早发型阿尔茨海默病患者的斜率比晚发型患者更陡。早发型组在CDR 0.5-1时出现快速下降,而晚发型组在CDR 2-3时出现类似变化。早发型患者比晚发型患者需要更严重的代谢减退才能达到相同的痴呆严重程度,这可能反映出年轻受试者比老年受试者具有更大的功能储备。或者,代谢下降曲线表明,早发型患者在葡萄糖代谢降低方面可能比晚发型患者进展更快。