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Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup.修订的阿尔茨海默病诊断和分期标准:阿尔茨海默病协会工作组。
Alzheimers Dement. 2024 Aug;20(8):5143-5169. doi: 10.1002/alz.13859. Epub 2024 Jun 27.
2
Tau accumulation and its spatial progression across the Alzheimer's disease spectrum.tau蛋白积累及其在阿尔茨海默病谱系中的空间进展。
Brain Commun. 2024 Feb 7;6(1):fcae031. doi: 10.1093/braincomms/fcae031. eCollection 2024.
3
Amidst an amygdala renaissance in Alzheimer's disease.在阿尔茨海默病的杏仁核复兴中。
Brain. 2024 Mar 1;147(3):816-829. doi: 10.1093/brain/awad411.
4
Biostatistical Estimation of Tau Threshold Hallmarks (BETTH) Algorithm for Human Tau PET Imaging Studies.用于人类 Tau PET 成像研究的 Tau 阈值特征的生物统计学估计(BETTH)算法。
J Nucl Med. 2023 Nov;64(11):1798-1805. doi: 10.2967/jnumed.123.265941. Epub 2023 Sep 14.
5
A two-step workflow based on plasma p-tau217 to screen for amyloid β positivity with further confirmatory testing only in uncertain cases.基于血浆 p-tau217 的两步工作流程,对淀粉样β 阳性进行筛选,仅对不确定病例进行进一步确认性检测。
Nat Aging. 2023 Sep;3(9):1079-1090. doi: 10.1038/s43587-023-00471-5. Epub 2023 Aug 31.
6
CenTauR: Toward a universal scale and masks for standardizing tau imaging studies.CenTauR:迈向用于标准化tau成像研究的通用量表和掩膜。
Alzheimers Dement (Amst). 2023 Jul 7;15(3):e12454. doi: 10.1002/dad2.12454. eCollection 2023 Jul-Sep.
7
The Use of Tau PET to Stage Alzheimer Disease According to the Braak Staging Framework.使用 Tau PET 根据 Braak 分期框架分期阿尔茨海默病。
J Nucl Med. 2023 Aug;64(8):1171-1178. doi: 10.2967/jnumed.122.265200. Epub 2023 Jun 15.
8
Amyloid and tau PET-positive cognitively unimpaired individuals are at high risk for future cognitive decline.淀粉样蛋白和 tau 正电子发射断层扫描(PET)阳性、认知正常的个体未来认知能力下降的风险较高。
Nat Med. 2022 Nov;28(11):2381-2387. doi: 10.1038/s41591-022-02049-x. Epub 2022 Nov 10.
9
The AHEAD 3-45 Study: Design of a prevention trial for Alzheimer's disease.AHEAD 3-45 研究:阿尔茨海默病预防试验设计。
Alzheimers Dement. 2023 Apr;19(4):1227-1233. doi: 10.1002/alz.12748. Epub 2022 Aug 15.
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Association of Elevated Amyloid and Tau Positron Emission Tomography Signal With Near-Term Development of Alzheimer Disease Symptoms in Older Adults Without Cognitive Impairment.在认知功能正常的老年人中,淀粉样蛋白和tau 正电子发射断层扫描信号升高与近期阿尔茨海默病症状的发展相关。
JAMA Neurol. 2022 Oct 1;79(10):975-985. doi: 10.1001/jamaneurol.2022.2379.

在tau 影像学研究中,非痴呆个体 tau 阈值的实施和评估作为认知下降的预测因子。

Implementation and Assessment of Tau Thresholds in Non-Demented Individuals as Predictors of Cognitive Decline in Tau Imaging Studies.

机构信息

Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

J Alzheimers Dis. 2024;100(s1):S75-S92. doi: 10.3233/JAD-240543.

DOI:10.3233/JAD-240543
PMID:39121123
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11776372/
Abstract

BACKGROUND

Tau accumulation in Alzheimer's disease is associated with short term clinical progression and faster rates of cognitive decline in individuals with high amyloid-β deposition. Defining an optimal threshold of tau accumulation predictive of cognitive decline remains a challenge.

OBJECTIVE

We tested the ability of regional tau PET sensitivity and specificity thresholds to predict longitudinal cognitive decline. We also tested the predictive performance of thresholds in the proposed new NIA-AA biological staging for Alzheimer's disease where multiple levels of tau positivity are used to stage participants.

METHODS

18F-flortaucipir scans from 301 non-demented participants were processed and sampled. Four cognitive measures were assessed longitudinally. Regional standardized uptake value ratios were split into infra- and suprathreshold groups at baseline using previously derived thresholds. Survival analysis, log rank testing, and Generalized Estimation Equations assessed the relationship between the application of regional sensitivity/specificity thresholds and change in cognitive measures as well as tau threshold performance in predicting cognitive decline within the new NIA-AA biological staging.

RESULTS

The meta temporal region was best for predicting risk of short-term cognitive decline in suprathreshold, as compared to infrathreshold participants. When applying multiple levels of tau positivity, each subsequent level of tau identified cognitive decline at earlier timepoints.

CONCLUSIONS

When using 18F-flortaucipir, meta temporal suprathreshold classification was associated with increased risk of cognitive decline, suggesting that abnormal tau deposition in the cortex predicts decline. Likewise, the application of multiple levels of tau clearly predicts the distinctive cognitive trajectories in the new NIA-AA biological staging framework.

摘要

背景

阿尔茨海默病患者脑中 tau 蛋白的积累与短期临床进展以及淀粉样蛋白-β 沉积较高个体的认知能力下降速度更快有关。定义 tau 蛋白积累预测认知能力下降的最佳阈值仍然是一个挑战。

目的

我们测试了区域 tau PET 敏感性和特异性阈值预测纵向认知能力下降的能力。我们还测试了在新的 NIA-AA 阿尔茨海默病生物学分期中使用多个 tau 阳性水平对参与者进行分期的情况下,tau 积累阈值的预测性能。

方法

对 301 名非痴呆参与者的 18F-flortaucipir 扫描进行了处理和采样。四项认知指标进行了纵向评估。在基线时,使用以前得出的阈值,将区域标准化摄取值比分为亚阈值和超阈值组。生存分析、对数秩检验和广义估计方程评估了在新的 NIA-AA 生物学分期中,应用区域敏感性/特异性阈值与认知测量变化之间的关系,以及 tau 阈值在预测认知下降方面的表现。

结果

与亚阈值组相比,meta 时间区域在超阈值组中预测短期认知下降风险的表现最佳。当应用多个 tau 阳性水平时,每个后续的 tau 水平都在更早的时间点识别出认知下降。

结论

在使用 18F-flortaucipir 时,meta 时间超阈值分类与认知下降风险增加相关,这表明皮质中的异常 tau 沉积预测下降。同样,多个 tau 水平的应用清楚地预测了新的 NIA-AA 生物学分期框架中的独特认知轨迹。