Center for Molecular Neurobiology, Department of Molecular and Cellular Biochemistry, The Ohio State University College of Medicine, Columbus, USA.
Curr Alzheimer Res. 2010 May;7(3):230-4. doi: 10.2174/156720510791050894.
Alzheimer's disease is diagnosed by postmortem detection of pathological lesions that accumulate in specific brain regions. Although the presence of both beta-amyloid plaques and tau-bearing neurofibrillary lesions defines Alzheimer's disease, the distribution of neurofibrillary lesions alone correlates strongly with neurodegeneration and cognitive decline. A whole-brain imaging test capable of detecting these lesions in premortem cases could have great potential for staging and differentially diagnosing Alzheimer's disease. Here we discuss the challenges in developing a whole-brain imaging approach for detection of this intracellular target.
阿尔茨海默病是通过死后检测在特定大脑区域积累的病理性病变来诊断的。虽然β-淀粉样斑块和携带 tau 的神经原纤维缠结病变的存在定义了阿尔茨海默病,但神经原纤维缠结病变的分布与神经退行性变和认知能力下降密切相关。一种能够在生前病例中检测到这些病变的全脑成像测试,对于分期和鉴别诊断阿尔茨海默病具有很大的潜力。在这里,我们讨论了开发一种用于检测这种细胞内靶标的全脑成像方法所面临的挑战。