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The Relationship between Amyloid Deposition, Neurodegeneration, and Cognitive Decline in Dementia

机译:痴呆症中淀粉样蛋白沉积,神经变性和认知能力下降的关系

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Amyloid imaging has been clinically approved for measuring beta amyloid plaque load in patients being evaluated for Alzheimer's disease or other causes of cognitive decline. Here we explore a multidimensional approach to cognitive decline, where we situate amyloid plaque burden among a number of other relevant dimensions, such as aging, volume loss, other proteinopathies such as TDP43 and Lewy bodies, and functional reorganisation of cognitive brain systems. The multidimensional model incorporates a 'pure AD' trajectory, corresponding to e. g. monogenic Alzheimer's disease, but leaves room for other combinations of biomarker abnormalities (e. g. volume loss without amyloid positivity) and other trajectories. More tools will become available in the future that allow one to carve out a causal-mechanistic space for explaing cognitive decline in a personalized manner, enhancing progress towards more efficacious interventions.
机译:淀粉样蛋白成像已被临床批准用于测量正在评估阿尔茨海默氏病或​​其他认知功能下降原因的患者的β淀粉样蛋白斑块负荷。在这里,我们探索了一种认知衰退的多维方法,其中我们将淀粉样斑块负担置于许多其他相关维度中,例如衰老,体积减少,其他蛋白质病(例如TDP43和路易小体)以及认知脑系统的功能重组。多维模型包含了一个对应于e的“纯AD”轨迹。 G。单基因的阿尔茨海默氏病,但为其他生物标志物异常组合(例如没有淀粉样蛋白阳性的体积减少)和其他轨迹留有空间。未来将有更多工具可用,使人们能够以个性化的方式开辟解释认知下降的因果机制空间,从而促进朝着更有效干预的方向发展。

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