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Update on hypothetical model of Alzheimer’s disease biomarkers

机译:更新对阿尔茨海默氏病的生物标记物的假设模型

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摘要

In 2010, the authors published a hypothetical model of the major biomarkers of Alzheimer’s disease (AD). The model was received with interest because we described the temporal evolution of AD biomarkers in relation to each other and to the onset and progression of clinical symptoms. In the interim, evidence has accumulated that supports the major assumptions of this model. Evidence has also appeared that challenges some of the assumptions underlying our original model. Recent evidence has allowed us to modify our original model. Refinements include indexing subjects by time rather than clinical symptom severity; incorporating inter-subject variability in cognitive response to the progression of AD pathophysiology; modifications of the specific temporal ordering of some biomarkers; and, recognition that the two major proteinopathies underlying AD biomarker changes, Aβ and tau, may be initiated independently in late onset AD where we hypothesize that an incident Aβopathy can accelerate an antecedent tauopathy.
机译:2010年,作者发表了有关阿尔茨海默氏病(AD)主要生物标志物的假设模型。该模型之所以引起人们的兴趣,是因为我们描述了AD生物标志物相对于彼此以及临床症状的发作和发展的时间演变。在此期间,已经积累了支持该模型主要假设的证据。也有证据挑战了我们原始模型的某些假设。最近的证据使我们可以修改原始模型。改进包括按时间而不是临床症状严重性对受试者进行索引;将受试者间的变异性纳入对AD病理生理学进展的认知反应中;修改某些生物标志物的特定时间顺序;并且,认识到AD生物标志物变化的两个主要蛋白病,Aβ和tau,可能在AD晚期发作时独立引发,我们假设Aβ病可以加速先天性tau病。

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