Schaffer Cole, Sarad Nakia, DeCrumpe Ashton, Goswami Disha, Herrmann Sara, Morales Jose, Patel Parth, Osborne Jim
Keck Graduate Institute of Applied Life Sciences, Claremont, CA, USA.
Keck Graduate Institute of Applied Life Sciences, Claremont, CA, USA
J Lab Autom. 2015 Oct;20(5):589-600. doi: 10.1177/2211068214559979. Epub 2014 Nov 25.
Alzheimer's disease (AD) is a neurodegenerative disease that inhibits cognitive functions and has no cure. This report reviews the current diagnostic standards for AD with an emphasis on early diagnosis using the cerebrospinal fluid (CSF) biomarkers amyloid-beta, t-tau, and p-tau and fluorodeoxyglucose positron emission tomography imaging. Abnormal levels of these CSF biomarkers and decreased cerebral uptake of glucose have recently been used in the early diagnosis of AD in experimental studies. These promising biomarkers can be measured using immunoassays performed in singleplex or multiplex formats. Although presently, there are no Food and Drug Administration-approved in vitro diagnostics (IVDs) for early detection of AD, a multiplex immunoassay measuring a panel of promising AD biomarkers in CSF may be a likely IVD candidate for the clinical AD diagnostic market. Specifically, the INNO-BIA AlzBio3 immunoassay kit, performed using bead arrays on the xMAP Luminex analyzer, allows simultaneous quantification of amyloid-beta, t-tau, and p-tau biomarkers. AD biomarkers can also be screened using enzyme-linked immunosorbent assays that are offered as laboratory-developed tests.
阿尔茨海默病(AD)是一种抑制认知功能且无法治愈的神经退行性疾病。本报告回顾了AD的当前诊断标准,重点是使用脑脊液(CSF)生物标志物β-淀粉样蛋白、总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)以及氟脱氧葡萄糖正电子发射断层扫描成像进行早期诊断。这些CSF生物标志物的异常水平以及大脑葡萄糖摄取减少最近已在实验研究中用于AD的早期诊断。这些有前景的生物标志物可以使用单重或多重形式的免疫测定法进行测量。虽然目前尚无美国食品药品监督管理局批准的用于AD早期检测的体外诊断(IVD)产品,但一种测量CSF中一组有前景的AD生物标志物的多重免疫测定法可能是临床AD诊断市场上很有可能的IVD候选产品。具体而言,使用xMAP Luminex分析仪上的微珠阵列进行的INNO-BIA AlzBio3免疫测定试剂盒可同时定量β-淀粉样蛋白、t-tau和p-tau生物标志物。AD生物标志物也可以使用作为实验室研发测试提供的酶联免疫吸附测定法进行筛选。