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血浆S100β和神经元特异性烯醇化酶水平与多发性硬化症的病情进展

Plasma S100beta and NSE levels and progression in multiple sclerosis.

作者信息

Koch Marcus, Mostert Jop, Heersema Dorothea, Teelken Albert, De Keyser Jacques

机构信息

Department of Neurology, University Medical Centre Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands.

出版信息

J Neurol Sci. 2007 Jan 31;252(2):154-8. doi: 10.1016/j.jns.2006.11.012. Epub 2006 Dec 21.

Abstract

Plasma levels of the glial cell marker S100beta and the neuronal marker neuron-specific enolase (NSE) are elevated in various conditions of central nervous system damage. In this study we investigated whether plasma levels of S100beta and NSE are related to disease progression in multiple sclerosis (MS). Plasma levels of S100beta and NSE were measured in 25 patients with relapsing remitting MS (RRMS), 23 with secondary progressive MS (SPMS) and 16 with primary progressive MS (PPMS). All MS patients were in a clinically stable phase. Progression and disability were evaluated during a follow-up period of five years. We found that plasma NSE levels were lower in patients with clinically relevant worsening on the Expanded Disability Status Scale (EDSS), defined as 1 point increase from EDSS <6.0 or 0.5 point increase from EDSS> or =6 after five years (p=0.042), and in patients with a progressive disease course (p=0.01). There was a significant negative correlation between plasma NSE levels and both EDSS and Multiple Sclerosis Severity Status (MSSS) scores at baseline and after five years of follow-up (r=-0.33 and -0.38, p=0.027 and 0.003). There were no significant differences between patient groups in plasma S100beta levels. Plasma NSE levels appear inversely related to disease progression in MS.

摘要

在中枢神经系统损伤的各种情况下,神经胶质细胞标志物S100β和神经元标志物神经元特异性烯醇化酶(NSE)的血浆水平会升高。在本研究中,我们调查了S100β和NSE的血浆水平是否与多发性硬化症(MS)的疾病进展相关。对25例复发缓解型MS(RRMS)患者、23例继发进展型MS(SPMS)患者和16例原发进展型MS(PPMS)患者测量了S100β和NSE的血浆水平。所有MS患者均处于临床稳定期。在五年的随访期内评估疾病进展和残疾情况。我们发现,在扩展残疾状态量表(EDSS)上有临床相关恶化的患者中,血浆NSE水平较低,临床相关恶化定义为五年后EDSS<6.0时增加1分或EDSS≥6时增加0.5分(p=0.042),在疾病呈进展病程的患者中也是如此(p=0.01)。在基线和随访五年后,血浆NSE水平与EDSS和多发性硬化症严重程度状态(MSSS)评分之间均存在显著负相关(r=-0.33和-0.38,p=0.027和0.003)。患者组之间的血浆S100β水平无显著差异。血浆NSE水平似乎与MS的疾病进展呈负相关。

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