van Engelen B G, Lamers K J, Gabreels F J, Wevers R A, van Geel W J, Borm G F
Department of Neurology, University Hospital Nijmegen, The Netherlands.
Clin Chem. 1992 Jun;38(6):813-6.
Studies on cerebrospinal fluid (CSF) concentrations of neuron-specific enolase (NSE), S-100 protein, and myelin basic protein (MBP) in patients with neurological lesions indicate a quantitative relation between the degree of cell damage in the central nervous system (CNS) and the concentration of these CNS-specific proteins in CSF. Thus NSE, S-100, and MBP could be of use as markers for destructive processes in the CNS. We collected 937 specimens of CSF from children and adults (from newborns to age 91 years) who were undergoing a diagnostic lumbar puncture for several clinical indications. Of these, 79 samples from subjects ranging in age from 0.7 to 66 years could be used retrospectively to construct a reference interval according to our criteria. In these 79 samples no sex dependency existed. The relative increase of NSE, S-100, and MBP with age was similar (1% per year), suggesting a common underlying mechanism. These results emphasize the necessity of using age-matched reference values when the CNS-specific proteins are to be evaluated in neurological diseases. We also present three case histories to discuss the possible clinical relevance of the measurement of NSE, S-100, and MBP in children and adults.
对患有神经病变患者脑脊液(CSF)中神经元特异性烯醇化酶(NSE)、S-100蛋白和髓鞘碱性蛋白(MBP)浓度的研究表明,中枢神经系统(CNS)细胞损伤程度与CSF中这些CNS特异性蛋白浓度之间存在定量关系。因此,NSE、S-100和MBP可用作CNS破坏性过程的标志物。我们收集了937份来自儿童和成人(从新生儿到91岁)的脑脊液样本,这些患者因多种临床指征正在接受诊断性腰椎穿刺。其中,79份来自年龄在0.7岁至66岁之间受试者的样本可根据我们的标准进行回顾性分析,以构建参考区间。在这79份样本中,不存在性别依赖性。NSE、S-100和MBP随年龄的相对增加相似(每年1%),提示存在共同的潜在机制。这些结果强调了在评估神经疾病中CNS特异性蛋白时使用年龄匹配参考值的必要性。我们还展示了三个病例,以讨论在儿童和成人中测量NSE、S-100和MBP的可能临床意义。