Blennow Kaj, Galasko Douglas
Dept. of Clinical Neuroscience, Unit of Neurochemistry, University of Göteborg, Sweden.
The Medical Research Council, Sweden.
EJIFCC. 2000 Mar 21;12(1):11-20. eCollection 2000 Mar.
In view of current (AChE inhibitors) and future (e.g. anti-Aβ aggregators), development and evaluation of cerebrospinal fluid (CSF) biomarkers for Alzheimer's disease (AD) has become a rapidly growing research field. Diagnostic biomarkers for AD would be especially valuable as aids in the diagnosis early in the course of the disease, when correct diagnosis is difficult, and when therapeutic compounds have the greatest potential of being effective. This paper reviews CSF biomarkers for AD, with emphasis on their role in the clinical diagnosis, and methodological aspects of importance for developing such analyses. Today, two biochemical markers, CSF-tau and CSF-Aβ42, perform satisfactory enough to have a role in the clinical workup of patients dementia, if used together with the cumulative information from clinical information and brain-imaging techniques. These markers are especially useful to discriminate early or incipient AD from age-associated memory impairment, depression, and some secondary dementias.
鉴于当前的(乙酰胆碱酯酶抑制剂)以及未来的(例如抗淀粉样蛋白β聚集剂)药物研发情况,阿尔茨海默病(AD)脑脊液(CSF)生物标志物的开发与评估已成为一个迅速发展的研究领域。AD的诊断生物标志物作为疾病早期诊断的辅助手段将具有特别重要的价值,因为在疾病早期正确诊断困难,而治疗性化合物此时具有最大的有效潜力。本文综述了AD的脑脊液生物标志物,重点阐述其在临床诊断中的作用以及开展此类分析的重要方法学方面。如今,两种生化标志物,即脑脊液总tau蛋白(CSF-tau)和脑脊液淀粉样蛋白β42(CSF-Aβ42),如果与临床信息和脑成像技术的累积信息一起使用,在痴呆患者的临床检查中表现出足够令人满意的效果,足以发挥作用。这些标志物对于区分早期或初期AD与年龄相关的记忆障碍、抑郁症以及某些继发性痴呆尤为有用。