Translational Neuroimaging Laboratory, McGill Research Centre for Studies in Aging, Douglas Mental Health Institute, Le Centre intégré universitaire de santé et de services sociaux (CIUSSS) de l'Ouest de l'Île de Montréal, Montreal, Quebec, Canada.
Department of Neurology and Neurosurgery, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
Nat Aging. 2022 Jun;2(6):526-535. doi: 10.1038/s43587-022-00204-0. Epub 2022 Apr 25.
Gold-standard diagnosis of Alzheimer's disease (AD) relies on histopathological staging systems. Using the topographical information from [F]MK6240 tau positron-emission tomography (PET), we applied the Braak tau staging system to 324 living individuals. We used PET-based Braak stage to model the trajectories of amyloid-β, phosphorylated tau (pTau) in cerebrospinal fluid (pTau, pTau, pTau and pTau) and plasma (pTau and pTau), neurodegeneration and cognitive symptoms. We identified nonlinear AD biomarker trajectories corresponding to the spatial extent of tau-PET, with modest biomarker changes detectable by Braak stage II and significant changes occurring at stages III-IV, followed by plateaus. Early Braak stages were associated with isolated memory impairment, whereas Braak stages V-VI were incompatible with normal cognition. In 159 individuals with follow-up tau-PET, progression beyond stage III took place uniquely in the presence of amyloid-β positivity. Our findings support PET-based Braak staging as a framework to model the natural history of AD and monitor AD severity in living humans.
阿尔茨海默病(AD)的金标准诊断依赖于组织病理学分期系统。我们利用 [F]MK6240 tau 正电子发射断层扫描(PET)的拓扑信息,将 Braak tau 分期系统应用于 324 名在世个体。我们使用基于 PET 的 Braak 分期来模拟淀粉样蛋白-β、脑脊液中磷酸化 tau(pTau)的轨迹(pTau、pTau、pTau 和 pTau)以及血浆中的 pTau 和 pTau)、神经退行性变和认知症状。我们确定了与 tau-PET 空间范围相对应的非线性 AD 生物标志物轨迹,Braak 分期 II 可检测到适度的生物标志物变化,而在 III-IV 期则会发生显著变化,随后达到平台期。早期 Braak 分期与孤立性记忆障碍相关,而 Braak 分期 V-VI 与正常认知不兼容。在 159 名有后续 tau-PET 随访的个体中,仅在存在淀粉样蛋白-β阳性的情况下,才会出现 III 期以后的进展。我们的研究结果支持基于 PET 的 Braak 分期作为模型 AD 自然史和监测 AD 严重程度的框架。