Serum neurofilaments light chain as a diagnostic marker of multiple sclerosis

E. M. Kamenskikh, V. Alifirova, D. V. Pashkovskaya, M. Titova, E. Koroleva, L. Levchuk, S. A. Ivanova
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Abstract

Neurofilaments are the structural components of neuronal axons, therefore are increasingly used in the diagnosis and course evaluation of neurological diseases. Potential application in multiple sclerosis (MS) is disease diagnosis.The aim of this work was to assess the level of serum neurofilament light chains (sNFL) to analyze the diagnostic value in MS.Material and methods. The study group included patients diagnosed with MS (n = 93), mean age — 38.1 (33.6; 45.9) years, EDSS 4 (2; 5.0) points. 75 patients (80.7%) had a relapsing-remitting course (RRMS), 18 (19.3%) had a secondary progressive course (SPMS). The comparison group (n = 40) consisted of forty age- and sex- matched volunteers. The concentration of sNFL was determined by enzyme-linked immunosorbent assay using a multimodal microplate reader Thermo Scientific Varioskan LUX (The Core Facility “Medical Genomics”, Tomsk NRMC). Statistical processing was carried out in the Statistica 12.0, the Mann-Whitney coefficient and ROC curve were used.Results. The sNFL index in patients was higher than in the control group (2.08 (1.88; 2.23) and 1.96 (1.88; 2.08) pg/ml, p = 0.006). However, statistically significant differences were achieved with more than 5 years of MS duration. Sensitivity and specificity were 67.5% and 61.5%, respectively.Conclusion. The sNFL can`t be considered as an early biomarker in MS, so its use in the primary diagnosis of the disease is not appropriate.
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作为多发性硬化症诊断标志物的血清神经丝蛋白轻链
神经丝是神经元轴突的结构成分,因此越来越多地被用于神经系统疾病的诊断和病程评估。这项工作的目的是评估血清神经丝蛋白轻链(sNFL)的水平,分析其在多发性硬化症(MS)中的诊断价值。研究组包括确诊为多发性硬化症的患者(n = 93),平均年龄-38.1(33.6;45.9)岁,EDSS 4(2;5.0)分。75名患者(80.7%)为复发缓解期(RRMS),18名患者(19.3%)为继发性进展期(SPMS)。对比组(n = 40)由 40 名年龄和性别匹配的志愿者组成。采用酶联免疫吸附法测定 sNFL 的浓度,使用的是 Thermo Scientific Varioskan LUX 多模式微孔板阅读器(托木斯克国立医学中心 "医学基因组学 "核心设施)。统计处理在 Statistica 12.0 中进行,使用了 Mann-Whitney 系数和 ROC 曲线。患者的 sNFL 指数高于对照组(2.08 (1.88; 2.23) pg/ml 和 1.96 (1.88; 2.08) pg/ml,p = 0.006)。然而,多发性硬化症病程超过 5 年时,两者之间的差异具有统计学意义。敏感性和特异性分别为67.5%和61.5%。sNFL不能被视为多发性硬化症的早期生物标志物,因此将其用于疾病的初诊并不合适。
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来源期刊
Russian Neurological Journal
Russian Neurological Journal Medicine-Neurology (clinical)
CiteScore
0.40
自引率
0.00%
发文量
49
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