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纹状体淀粉样斑块密度可预测 Braak 神经纤维缠结分期和临床病理阿尔茨海默病:对淀粉样蛋白成像的影响。

Striatal amyloid plaque density predicts Braak neurofibrillary stage and clinicopathological Alzheimer's disease: implications for amyloid imaging.

机构信息

Banner Sun Health Research Institute, Sun City, AZ 85351, USA.

出版信息

J Alzheimers Dis. 2012;28(4):869-76. doi: 10.3233/JAD-2011-111340.

Abstract

Amyloid imaging may revolutionize Alzheimer's disease (AD) research and clinical practice but is critically limited by an inadequate correlation between cerebral cortex amyloid plaques and dementia. Also, amyloid imaging does not indicate the extent of neurofibrillary tangle (NFT) spread throughout the brain. Currently, the presence of dementia as well as a minimal brain load of both plaques and NFTs is required for the diagnosis of AD. Autopsy studies suggest that striatal amyloid plaques may be mainly restricted to subjects in higher Braak NFT stages that meet clinicopathological diagnostic criteria for AD. Striatal plaques, which are readily identified by amyloid imaging, might therefore be used to predict the presence of a higher Braak NFT stage and clinicopathological AD in living subjects. This study determined the sensitivity and specificity of striatal plaques for predicting a higher Braak NFT stage and clinicopathological AD in a postmortem series of 211 elderly subjects. Subjects included 87 clinicopathologically classified as non-demented elderly controls and 124 with AD. A higher striatal plaque density score (moderate or frequent) had 95.8% sensitivity, 75.7% specificity for Braak NFT stage V or VI and 85.6% sensitivity, 86.2% specificity for the presence of dementia and clinicopathological AD (National Institute on Aging - Reagan Institute "intermediate" or "high"). Amyloid imaging of the striatum may be useful as a predictor, in living subjects, of Braak NFT stage and the presence or absence of dementia and clinicopathological AD. Validation of this hypothesis will require autopsy studies of subjects that had amyloid imaging during life.

摘要

淀粉样蛋白成像可能会彻底改变阿尔茨海默病(AD)的研究和临床实践,但由于大脑皮层淀粉样斑块与痴呆之间的相关性不足,该技术受到了严重限制。此外,淀粉样蛋白成像并不能显示整个大脑中神经原纤维缠结(NFT)的扩散程度。目前,AD 的诊断需要存在痴呆以及斑块和 NFT 的大脑负荷最小。尸检研究表明,纹状体淀粉样斑块可能主要局限于符合 AD 临床病理诊断标准的更高 Braak NFT 阶段的受试者中。因此,通过淀粉样蛋白成像容易识别的纹状体斑块,可能被用于预测更高 Braak NFT 阶段和临床病理 AD 的存在。本研究通过对 211 名老年受试者的尸检系列,确定了纹状体斑块预测更高 Braak NFT 阶段和临床病理 AD 的敏感性和特异性。受试者包括 87 名临床病理分类为非痴呆老年对照组和 124 名 AD 患者。较高的纹状体斑块密度评分(中度或频繁)对 Braak NFT 阶段 V 或 VI 的敏感性为 95.8%,特异性为 75.7%,对痴呆和临床病理 AD(国家老龄化研究所 - 里根研究所“中等”或“高”)的存在的敏感性为 85.6%,特异性为 86.2%。纹状体的淀粉样蛋白成像可能可作为预测活体受试者 Braak NFT 阶段以及痴呆和临床病理 AD 存在与否的指标。该假说的验证需要对在生前进行过淀粉样蛋白成像的受试者进行尸检研究。

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