tau蛋白测定在克雅氏病诊断中的附加价值。

Edit Katalin Cseh, Gábor Veres, Krisztina Danics, Levente Szalárdy, Nikolett Nánási, Péter Klivényi, László Vécsei, Dénes Zádori
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引用次数: 4

摘要

由于克雅氏病(Creutzfeldt-Jakob disease, CJD)的明确诊断目前只能通过尸检来提供,因此在活体患者中特别需要精细的诊断工具,以尽早实现准确诊断。本研究的目的是对快速进展性痴呆患者脑脊液(CSF)中总Tau (tTau)和一些其他生物标志物的测量在CJD诊断工作中的效用进行初步回顾性分析。除了评估相关临床数据以及脑电图和脑磁共振成像结果外,我们还利用Western blot技术和酶联免疫吸附法检测了2004-2017年塞格德大学神经内科诊断为快速进展性痴呆的19例脑脊液中14-3-3蛋白的存在和tTau水平。本初步研究为14-3-3提供100%的敏感性,有趣的是,只有40%的特异性支持CJD的临床诊断。对于tTau,根据应用的截止水平,计算灵敏度值为100%或83%,而特异性值为71%或86%。14-3-3的特异性较差,与文献资料不符,可能是非朊病毒疾病队列中患者较少,以组织损伤较大的疾病为主,而tTau具有较好的敏感性和特异性值。这些和新的化学生物标志物的联合应用可以将灵敏度和特异性提高到所需的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Additional value of tau protein measurement in the diagnosis of Creutzfeldt-Jakob disease.

Since the definite diagnosis of Creutzfeldt-Jakob disease (CJD) can currently only be provided by autopsy, there is a special need for fine diagnostic tools in live patients to achieve accurate diagnosis as early as possible. The aim of this study was to perform a preliminary retrospective analysis on the utility of the measurement of total Tau (tTau) and some other biomarkers from the cerebrospinal fluid (CSF) of patients with rapidly progressive dementia in the diagnostic work up of CJD. Beside the assessment of relevant clinical data and the findings of electroencephalography and brain magnetic resonance imaging, the presence of 14-3-3 protein and the levels of tTau were determined by Western blot technique and enzyme-linked immunosorbent assay from the CSF of 19 patients diagnosed with rapidly progressive dementia between the period of 2004-2017 at the Department of Neurology, University of Szeged. This preliminary study provided 100% sensitivity for 14-3-3, and interestingly, only 40% specificity to support the clinical diagnosis of CJD. Regarding tTau, the sensitivity values were calculated to be 100% or 83%, whereas the specificity values were 71% or 86%, depending on the applied cut-off levels. The poor specificity of 14-3-3 is not in line with literature data and may be the result of the small number of patients in the cohort with non-prion disease, predominantly consisting of disorders with considerable tissue damage, whereas tTau presented good sensitivity and specificity values. The combined application of these and novel chemical biomarkers may increase both sensitivity and specificity to a desired level.

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