血液淀粉样蛋白水平可以作为阿尔茨海默病的生物标志物吗?

Yuan-Han Yang, R. Situmeang, P. A. Ong
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引用次数: 4

摘要

由于人口老龄化,阿尔茨海默病(AD)对社会的影响越来越大。即使在临床前阶段,早期准确的诊断对于优化AD管理和改善临床结果也是至关重要的。生物标志物,如脑脊液中的β淀粉样蛋白(Aβ)或tau蛋白,已被用作区分AD和非AD的可靠标志物,并预测临床结果,以实现这些目标。然而,考虑到CSF进入方法的侵入性,这些生物标志物在临床环境中没有广泛使用。血液Aβ被认为是一种替代的生物标志物,因为它的侵袭性比CSF小;然而,抽样异质性限制了其临床适用性。在这篇综述中,我们研究了血液Aβ作为AD的生物标志物,并探讨了如何促进Aβ作为成功管理AD的可行生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can blood amyloid levels be used as a biomarker for Alzheimer’s disease?
Alzheimer’s disease (AD) increasingly affects society due to aging populations. Even at pre‐clinical stages, earlier and accurate diagnoses are essential for optimal AD management and improved clinical outcomes. Biomarkers such as beta‐amyloid (Aβ) or tau protein in cerebrospinal fluid (CSF) have been used as reliable markers to distinguish AD from non‐AD, and predicting clinical outcomes, to attain these goals. However, given CSF access methods’ invasiveness, these biomarkers are not used extensively in clinical settings. Blood Aβ has been proposed as an alternative biomarker since it is less invasive than CSF; however, sampling heterogeneity has limited its clinical applicability. In this review, we investigated blood Aβ as a biomarker in AD and explored how Aβ can be facilitated as a viable biomarker for successful AD management.
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