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早期相11C-PIB PET显像探讨阿尔茨海默病患者脑功能网络改变
引用本文:李灿,徐白萱,张锦明,刘家金,富丽萍.早期相11C-PIB PET显像探讨阿尔茨海默病患者脑功能网络改变[J].中国医学影像技术,2018,34(11):1621-1626.
作者姓名:李灿  徐白萱  张锦明  刘家金  富丽萍
作者单位:中国人民解放军总医院核医学科, 北京 100853,中国人民解放军总医院核医学科, 北京 100853,中国人民解放军总医院核医学科, 北京 100853,中国人民解放军总医院核医学科, 北京 100853,中国人民解放军总医院核医学科, 北京 100853
基金项目:中国博士后科学基金(20090461433、2013M542515)。
摘    要:目的 探讨阿尔茨海默病(AD)和轻度认知功能障碍(MCI)患者11C-匹兹堡化合物(11C-pPIB)脑灌注网络改变。方法 对14例AD(AD组)、12例MCI(MCI组)和14名认知功能正常志愿者(对照组)行18F-FDG及11C-PIB双示踪剂PET显像,采用平行独立成分分析法(pICA)计算11C-pPIB和18F-FDG数据中高度相关的脑网络,以双样本t检验比较AD组与对照组间和MCI组与对照组间18F-FDG低代谢与11C-pPIB低灌注的差异,获得组间有差异的脑区。结果 11C-pPIB获得的脑灌注网络与18F-FDG代谢网络高度相关(r=0.92),并与默认网络(DMN)存在空间重叠。与对照组比较,AD组18F-FDG低代谢区与11C-pPIB低灌注区存在空间重叠,包括颞上回、边缘叶/海马旁回、顶上小叶、后扣带回和前扣带回;MCI组18F-FDG的低代谢脑区位于右侧直回/眶额回、左侧后扣带回、右侧颞下回和右侧顶下小叶/颞上回,11C-pPIB低灌注脑区为右侧顶下小叶。结论 AD患者11C-pPIB低灌注脑区与18F-FDG低代谢高度相关,并与DMN存在空间重叠。11C-pPIB显像可为诊断AD提供与18F-FDG显像互补的信息。

关 键 词:阿尔茨海默病  认知障碍  体层摄影术  发射型计算机  11C-匹兹堡化合物  氟脱氧葡萄糖F18
收稿时间:2018/7/13 0:00:00
修稿时间:2018/9/10 0:00:00

Early-phase 11C-PIB PET imaging in identifying brain network alterations in Alzheimer disease
LI Can,XU Baixuan,ZHANG Jinming,LIU Jiajin and FU Liping.Early-phase 11C-PIB PET imaging in identifying brain network alterations in Alzheimer disease[J].Chinese Journal of Medical Imaging Technology,2018,34(11):1621-1626.
Authors:LI Can  XU Baixuan  ZHANG Jinming  LIU Jiajin and FU Liping
Institution:Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China,Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China,Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China,Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China and Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China
Abstract:Objective To observe the brain network changes in patients with Alzheimer disease (AD) and mild cognitively impaired (MCI) using early-phase 11C-PIB (Pittsburgh compound B, pPIB) PET scan. Methods A total of 14 patients with AD (AD group), 12 patients with MCI (MCI group) and 12 healthy controls (control group) underwent 11C-PIB and 18F-FDG PET/CT scaning. The parallel independent component analysis (pICA) was used to calculate strong correlated brain networks between AD and MCI patients. The differences of hypometabolic FDG and low perfusion 11C-pPIB areas were compared among AD, MCI and control groups with two-sample t-test. Results The brain perfusion network derived from 11C-pPIB PET was strongly correlated with brain metabolic network derived from 18F-FDG PET (r=0.92), both co-localized with the default mode network (DMN). Particularly, compared with control group, a decreased 18F-FDG uptake was shown to correlate with a lower regional perfusion of 11C-pPIB in superior temporal gyrus, limbic lobe/parahippocampal gyrus, superior parietal lobule, anterior cingulate cortex and posterior cingulate cortex in AD group; in MCI group, 18F-FDG uptake decreased in the right rectal gyrus/orbit frontal cortex, left posterior cingulate cortex, right inferior temporal gyrus and right inferior parietal lobule/superior temporal gyrus, while hypoperfusion of 11C-pPIB was only detected in the right inferior parietal lobule. Conclusion There is strong relationship between hypometabolic 18F-FDG and low perfusion 11C-pPIB areas in AD patients, both co-localized with the DMN. 11C-pPIB can provide complementary information for 18F-FDG examination in AD.
Keywords:Alzheimer disease  Cognition disorders  Tomography  emission-computed  11C-Pittsburgh compound B  Fludeoxyglucose F 18
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