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CSF 神经胶质标志物与肌萎缩侧索硬化症的生存相关。

CSF glial markers correlate with survival in amyotrophic lateral sclerosis.

机构信息

Department of Neurology, University of Ulm, Ulm, Germany.

出版信息

Neurology. 2010 Mar 23;74(12):982-7. doi: 10.1212/WNL.0b013e3181d5dc3b.

Abstract

BACKGROUND

In neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), CSF biomarkers are increasingly studied to evaluate their relevance for differential diagnosis, disease progression, and understanding of pathophysiologic processes.

OBJECTIVE

To identify a biomarker profile of neuronal and glial CSF proteins to discriminate ALS from other motor neuron diseases (MND) and to assess whether baseline levels of CSF measures in ALS are associated with the course of the disease.

METHODS

A total of 122 consecutive subjects with MND were included in this cross-sectional study (ALS, n = 75; lower motor neuron syndrome, n = 39; upper motor neuron diseases, n = 8). Clinical follow-up included 76 patients. We determined baseline levels of protein tau and astroglial S100beta in CSF and microglial sCD14 in CSF and serum in relation to diagnosis, duration of disease, and survival.

RESULTS

CSF tau was significantly elevated in ALS and upper motor neuron diseases as compared to lower motor neuron diseases and controls. CSF S100beta levels were significantly lower in lower motor neuron diseases as compared to other MND. CSF concentrations of S100beta and sCD14 correlated with the survival time in patients with ALS.

CONCLUSIONS

In motor neuron diseases, CSF tau elevation indicates the degeneration of upper motor neurons, while S100 beta and sCD14 may indicate the activation of CNS glial cells. Because S100beta and sCD14 concentrations correlate with survival in amyotrophic lateral sclerosis (ALS), we suppose that the combination of both markers may be useful to obtain prognostic information in patients with ALS.

摘要

背景

在神经退行性疾病(如肌萎缩侧索硬化症,ALS)中,CSF 生物标志物的研究越来越多,以评估其对鉴别诊断、疾病进展和病理生理过程的理解的相关性。

目的

确定神经元和神经胶质 CSF 蛋白的生物标志物谱,以区分 ALS 与其他运动神经元疾病(MND),并评估 ALS 患者的 CSF 测量值是否与疾病的病程相关。

方法

本横断面研究共纳入 122 例连续 MND 患者(ALS,n = 75;下运动神经元综合征,n = 39;上运动神经元疾病,n = 8)。临床随访包括 76 例患者。我们测定了 CSF 中蛋白 tau 和神经胶质 S100beta 以及 CSF 和血清中微胶质 sCD14 的基线水平,与诊断、疾病持续时间和生存相关。

结果

与下运动神经元疾病和对照组相比,CSF tau 在 ALS 和上运动神经元疾病中显著升高。与其他 MND 相比,下运动神经元疾病的 CSF S100beta 水平显著降低。CSF S100beta 和 sCD14 浓度与 ALS 患者的生存时间相关。

结论

在运动神经元疾病中,CSF tau 的升高表明上运动神经元的退化,而 S100beta 和 sCD14 可能表明中枢神经系统胶质细胞的激活。由于 S100beta 和 sCD14 浓度与 ALS 患者的生存相关,我们假设这两种标志物的组合可能有助于为 ALS 患者提供预后信息。

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