Green A J, Thompson E J, Stewart G E, Zeidler M, McKenzie J M, MacLeod M A, Ironside J W, Will R G, Knight R S
The National Creutzfeldt-Jakob Disease Surveillance Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
J Neurol Neurosurg Psychiatry. 2001 Jun;70(6):744-8. doi: 10.1136/jnnp.70.6.744.
The detection of the protein 14-3-3 in the CSF has been shown to be a reliable and sensitive marker for sporadic Creutzfeldt-Jakob disease (CJD). Other brain-specific proteins such as neuron specific enolase (NSE), S-100b, and tau protein have also been reported to be increased in the CSF of patients with sporadic CJD. In 1996 a variant of CJD (vCJD) was described which is likely to be causally linked to the bovine spongiform encephalopathy agent. This study reports and compares the findings of CSF brain specific protein analysis in 45 patients with vCJD and in 34 control patients.
The CSF from 45 patients with vCJD and 34 controls were investigated for the presence of 14-3-3 by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting with chemiluminescent detection. Tau protein, S-100b, and NSE concentrations in CSF were measured using enzyme immunoassays.
Protein 14-3-3 was detected in the CSF of 22/45 patients with vCJD and in 3/34 controls. The mean concentrations of NSE, S-100b, and tau protein in CSF were significantly raised in patients with vCJD compared with controls. The positive predictive value of CSF 14-3-3 was 86% and the negative predictive value was 63%. These values are lower than those reported for sporadic CJD. An increased CSF tau had a positive predictive value of 93% and a negative predictive value of 81%. The combination of CSF 14-3-3 and/or increased CSF tau had a positive predictive value of 91% and a negative predictive value of 84%.
CSF protein 14-3-3 is not as useful a marker for vCJD as it is for sporadic CJD. Increased concentration of CSF tau was found to be a sensitive marker of vCJD but as concentrations may be increased in many forms of non-CJD dementia, this may limit its usefulness as a diagnostic test.
脑脊液中蛋白质14 - 3 - 3的检测已被证明是散发性克雅氏病(CJD)的可靠且敏感的标志物。其他脑特异性蛋白质,如神经元特异性烯醇化酶(NSE)、S - 100b和tau蛋白,也有报道称在散发性CJD患者的脑脊液中含量升高。1996年描述了一种变异型克雅氏病(vCJD),它可能与牛海绵状脑病病原体存在因果联系。本研究报告并比较了45例vCJD患者和34例对照患者脑脊液脑特异性蛋白质分析的结果。
通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)和化学发光检测的蛋白质印迹法,对45例vCJD患者和34例对照的脑脊液进行14 - 3 - 3检测。使用酶免疫测定法测量脑脊液中tau蛋白、S - 100b和NSE的浓度。
在45例vCJD患者中的22例和34例对照中的3例脑脊液中检测到了蛋白质14 - 3 - 3。与对照组相比,vCJD患者脑脊液中NSE、S - 100b和tau蛋白的平均浓度显著升高。脑脊液14 - 3 - 3的阳性预测值为86%,阴性预测值为63%。这些值低于散发性CJD的报道值。脑脊液tau升高的阳性预测值为93%,阴性预测值为81%。脑脊液14 - 3 - 3和/或脑脊液tau升高的组合阳性预测值为91%,阴性预测值为84%。
脑脊液蛋白质14 - 3 - 3作为vCJD的标志物不如其作为散发性CJD的标志物有用。发现脑脊液tau浓度升高是vCJD的敏感标志物,但由于在许多非CJD痴呆形式中浓度可能升高,这可能会限制其作为诊断测试的实用性。