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β-淀粉样蛋白在衰老和阿尔茨海默病中的积累的时间动态。

Temporal Dynamics of β-Amyloid Accumulation in Aging and Alzheimer Disease.

机构信息

From the Helen Wills Neuroscience Institute, University of California, Berkeley; and Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA.

出版信息

Neurology. 2021 Mar 2;96(9):e1347-e1357. doi: 10.1212/WNL.0000000000011524. Epub 2021 Jan 6.

Abstract

OBJECTIVE

To understand the time course of β-amyloid (Aβ) deposition in the brain, which is crucial for planning therapeutic trials of Aβ-lowering therapies in Alzheimer disease (AD).

METHODS

Two samples of participants from the Alzheimer's Disease Neuroimaging Initiative were studied with [F]Florbetapir (FBP) Aβ PET and followed for up to 9 years. Sample A included 475 cognitively normal (CN) older people and those with mild cognitive impairment (MCI) and AD and sample B included 220 CN Aβ- individuals. We examined the trajectory of FBP over time in sample A and the incidence rate of conversion from negative to positive Aβ PET scans in sample B.

RESULTS

The relationship between time and brain Aβ was sigmoidal, taking 6.4 years to transition from amyloid negative to positive and another 13.9 years to the onset of MCI. Aβ deposition rates began to slow only 3.8 years after reaching the positivity threshold. The incidence rate for scan positivity was 38/1,000 person-years, and factors associated with conversion were age, baseline FBP, and being a female ε4 carrier. Among CN Aβ- individuals, FBP slopes were associated with rates of memory decline and brain tau measured with [F]Flortaucipir PET 5 years after baseline.

CONCLUSIONS

Lowering brain Aβ must be accomplished early in the evolution of AD. Transitions of PET scans from Aβ- to Aβ+ should be predictable, and it is reasonable to expect that lowering rates of Aβ even in early stages could produce clinically significant benefits.

摘要

目的

了解大脑中β-淀粉样蛋白(Aβ)沉积的时间进程,这对于规划阿尔茨海默病(AD)中降低 Aβ 疗法的治疗试验至关重要。

方法

使用 [F]Florbetapir(FBP)Aβ PET 对来自阿尔茨海默病神经影像学倡议的两个参与者样本进行了研究,并随访了长达 9 年。样本 A 包括 475 名认知正常(CN)的老年人以及有轻度认知障碍(MCI)和 AD 的患者,样本 B 包括 220 名 CN Aβ-个体。我们检查了样本 A 中 FBP 随时间的轨迹以及样本 B 中从阴性转为阳性 Aβ PET 扫描的转化率发生率。

结果

大脑 Aβ 与时间之间的关系呈 S 型,从 Aβ 阴性到阳性转变需要 6.4 年,从 MCI 发病又需要 13.9 年。在达到阳性阈值后仅 3.8 年后,Aβ 沉积率才开始放缓。扫描阳性的发生率为 38/1000 人年,与转化相关的因素包括年龄、基线 FBP 和作为女性 ε4 携带者。在 CN Aβ-个体中,FBP 斜率与基线后 5 年使用 [F]Flortaucipir PET 测量的记忆下降率和脑 tau 相关。

结论

必须在 AD 演变的早期阶段降低大脑 Aβ。从 Aβ-到 Aβ+的 PET 扫描转变应该是可预测的,并且可以合理地期望即使在早期阶段降低 Aβ 水平也能产生有临床意义的益处。

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