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阿尔茨海默病的生物标志物。

Biomarkers of Alzheimer Disease.

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO.

Department of Neurology, Washington University School of Medicine, St. Louis, MO.

出版信息

J Appl Lab Med. 2020 Jan 1;5(1):194-208. doi: 10.1373/jalm.2019.030080.

Abstract

BACKGROUND

Alzheimer disease (AD) was once a clinical diagnosis confirmed by postmortem autopsy. Today, with the development of AD biomarkers, laboratory assays to detect AD pathology are able to complement clinical diagnosis in symptomatic individuals with uncertain diagnosis. A variety of commercially available assays are performed as laboratory-developed tests, and many more are in development for both clinical and research purposes.

CONTENT

The role of laboratory medicine in diagnosing and managing AD is expanding; thus, it is important for laboratory professionals and ordering physicians to understand the strengths and limitations of both existing and emerging AD biomarker assays. In this review, we will provide an overview of the diagnosis of AD, discuss existing laboratory assays for AD and their recommended use, and examine the clinical performance of emerging AD biomarkers.

SUMMARY

The field of AD biomarker discovery and assay development is rapidly evolving, with recent studies promising to improve both the diagnosis of symptomatic individuals and enrollment and monitoring of asymptomatic individuals in research studies. However, care must be taken to ensure proper use and interpretation of these assays. For clinical purposes, these assays are meant to aid in diagnosis but are not themselves diagnostic. For individuals without symptoms, AD biomarker tests are still only appropriate for research purposes. Additionally, there are analytical challenges that require careful attention, especially for longitudinal use of AD tests.

摘要

背景

阿尔茨海默病(AD)曾经是通过尸检进行临床诊断后确诊的疾病。如今,随着 AD 生物标志物的发展,用于检测 AD 病理的实验室检测能够在症状不确定的个体中补充临床诊断。许多现有的用于临床和研究目的的 AD 生物标志物检测都是作为实验室开发的检测进行的,还有更多的正在开发中。

内容

实验室医学在 AD 的诊断和管理中的作用正在扩大;因此,实验室专业人员和开单医生了解现有和新兴 AD 生物标志物检测的优缺点非常重要。在这篇综述中,我们将概述 AD 的诊断,讨论现有的 AD 实验室检测及其推荐用途,并研究新兴 AD 生物标志物的临床性能。

总结

AD 生物标志物发现和检测方法的发展领域正在迅速发展,最近的研究有望改善有症状个体的诊断,并为无症状个体的入组和监测研究提供帮助。然而,必须注意确保这些检测的正确使用和解释。就临床而言,这些检测旨在辅助诊断,但本身并不能做出诊断。对于没有症状的个体,AD 生物标志物检测仍仅适用于研究目的。此外,还存在需要特别注意的分析挑战,尤其是对于 AD 检测的纵向使用。

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本文引用的文献

1
Agreement of amyloid PET and CSF biomarkers for Alzheimer's disease on Lumipulse.
Ann Clin Transl Neurol. 2019 Sep;6(9):1815-1824. doi: 10.1002/acn3.50873. Epub 2019 Aug 28.
2
High-precision plasma β-amyloid 42/40 predicts current and future brain amyloidosis.
Neurology. 2019 Oct 22;93(17):e1647-e1659. doi: 10.1212/WNL.0000000000008081. Epub 2019 Aug 1.
3
Performance of Fully Automated Plasma Assays as Screening Tests for Alzheimer Disease-Related β-Amyloid Status.
JAMA Neurol. 2019 Sep 1;76(9):1060-1069. doi: 10.1001/jamaneurol.2019.1632.
4
Plasma and CSF neurofilament light: Relation to longitudinal neuroimaging and cognitive measures.
Neurology. 2019 Jul 16;93(3):e252-e260. doi: 10.1212/WNL.0000000000007767. Epub 2019 Jun 10.
7
Method comparison study of the Elecsys® β-Amyloid (1-42) CSF assay versus comparator assays and LC-MS/MS.
Clin Biochem. 2019 Oct;72:7-14. doi: 10.1016/j.clinbiochem.2019.05.006. Epub 2019 May 23.
9
Blood-based molecular biomarkers for Alzheimer's disease.
Mol Brain. 2019 Mar 28;12(1):26. doi: 10.1186/s13041-019-0448-1.

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