神经丝轻链在中枢神经系统脱髓鞘条件:一个有前途的生物标志物

S. Bozzetti, S. Ferrari, A. Gajofatto, S. Mariotto
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引用次数: 6

摘要

神经丝是神经元细胞骨架的主要结构蛋白,按分子量分为重链、中间链和轻链。它们被释放到间质液和脑脊液(CSF)作为轴突损伤的结果。特别是,轻链(NfL)代表了最丰富和可溶的亚基,并且已被证明在炎症、退行性、血管或创伤性损伤患者的脑脊液中增加,与临床和放射活性相关。用高灵敏度单分子阵列测量血清NfL也获得了类似的结果,该方法可以可靠且可重复地测量血清中低NfL浓度。特别是,脑脊液和血清NfL值在多发性硬化症(MS)患者中具有很强的相关性,并且根据临床和放射活性已被证明在多发性硬化症和临床孤立综合征(CIS)患者中升高。NfL水平在近期复发的患者中升高,似乎可以预测认知障碍、长期预后和CIS向ms的转化。关于其他脱髓鞘疾病患者的少数可用数据表明,NfL水平在视神经脊髓炎谱系障碍和与发作严重程度相关的相关疾病中也升高,表明轴突损伤可能发生在这些疾病中。在此,我们报告并讨论了已发表的关于NfL作为中枢神经系统脱髓鞘疾病患者疾病活动性、临床结果和治疗反应的可能预测因子的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurofilament light chain in demyelinating conditions of the central nervous system: a promising biomarker
Neurofilaments are the major structural proteins of the neuronal cytoskeleton and are classified according to molecular weight into heavy, intermediate, and light chains. They are released into the interstitial fluid and cerebrospinal fluid (CSF) as a consequence of axonal damage. In particular, the light chain (NfL) represents the most abundant and soluble subunit and has been demonstrated to be increased in the CSF of patients with inflammatory, degenerative, vascular, or traumatic injuries in correlation with clinical and radiological activity. Similar results have been obtained measuring serum NfL with high-sensitivity single-molecule array, which enables reliable and repeatable measurement of the low NfL concentrations in serum. In particular, CSF and serum NfL values are strongly correlated in patients with multiple sclerosis (MS) and have been demonstrated to be increased in patients with MS and clinically isolated syndromes (CIS) in accordance with clinical and radiological activity. NfL levels increase in patients with a recent relapse and seem to predict cognitive impairment, longterm outcome, and conversion of CIS to MS. The few available data on patients with other demyelinating diseases suggest that NfL levels are also increased in neuromyelitis optica spectrum disorders and related conditions in correlation with attack severity, suggesting that axonal damage may occur in these disorders. We herein report and discuss published data on the role of NfL as a possible predictor of disease activity, clinical outcome and treatment response in patients with demyelinating conditions of the central nervous system.
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