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血浆 Aβ42/40 比值可检测阿尔茨海默病早期,并与 AB255 研究中的 CSF 和神经影像学生物标志物相关联。

Plasma Aβ42/40 Ratio Detects Early Stages of Alzheimer's Disease and Correlates with CSF and Neuroimaging Biomarkers in the AB255 Study.

机构信息

Pedro Pesini, PhD. Vía Hispanidad 21, 50009 Zaragoza, Spain; Telephone number: +34 976 796 562; Fax: (+34) 976 217 802; Email:

出版信息

J Prev Alzheimers Dis. 2019;6(1):34-41. doi: 10.14283/jpad.2018.41.

Abstract

BACKGROUND

Easily accessible biomarkers are needed for the early identification of individuals at risk of developing Alzheimer's disease (AD) in large population screening strategies.

OBJECTIVES

This study evaluated the potential of plasma β-amyloid (Aβ) biomarkers in identifying early stages of AD and predicting cognitive decline over the following two years.

DESIGN

Total plasma Aβ42/40 ratio (TP42/40) was determined in 83 cognitively normal individuals (CN) and 145 subjects with amnestic mild cognitive impairment (a-MCI) stratified by an FDG-PET AD-risk pattern.

RESULTS

Significant lower TP42/40 ratio was found in a-MCI patients compared to CN. Moreover, a-MCIs with a high-risk FDG-PET pattern for AD showed even lower plasma ratio levels. Low TP42/40 at baseline increased the risk of progression to dementia by 70%. Furthermore, TP42/40 was inversely associated with neocortical amyloid deposition (measured with PiB-PET) and was concordant with the AD biomarker profile in cerebrospinal fluid (CSF).

CONCLUSIONS

TP42/40 demonstrated value in the identification of individuals suffering a-MCI, in the prediction of progression to dementia, and in the detection of underlying AD pathology revealed by FDG-PET, Amyloid-PET and CSF biomarkers, being, thus, consistently associated with all the well-established indicators of AD.

摘要

背景

在大规模人群筛查策略中,需要易于获取的生物标志物来早期识别有患阿尔茨海默病(AD)风险的个体。

目的

本研究评估了血浆β-淀粉样蛋白(Aβ)生物标志物在识别 AD 早期阶段和预测随后两年认知能力下降方面的潜力。

设计

在 83 名认知正常个体(CN)和 145 名有遗忘型轻度认知障碍(a-MCI)的受试者中,测定总血浆 Aβ42/40 比值(TP42/40),并根据 FDG-PET AD 风险模式进行分层。

结果

与 CN 相比,a-MCI 患者的 TP42/40 比值明显降低。此外,具有 AD 高风险 FDG-PET 模式的 a-MCI 患者的血浆比值水平甚至更低。基线时低 TP42/40 使进展为痴呆的风险增加了 70%。此外,TP42/40 与新皮质淀粉样蛋白沉积(用 PiB-PET 测量)呈负相关,与脑脊液(CSF)中的 AD 生物标志物谱一致。

结论

TP42/40 在识别患有 a-MCI 的个体、预测向痴呆进展以及检测 FDG-PET、淀粉样蛋白-PET 和 CSF 生物标志物揭示的潜在 AD 病理方面具有价值,因此与所有公认的 AD 指标一致。

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