脑脊液神经丝光作为多发性硬化症临床标志物的探索一项基于登记的回顾性研究。

IF 5
Igal Rosenstein, Markus Axelsson, Lenka Novakova, Kaj Blennow, Henrik Zetterberg, Jan Lycke
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引用次数: 9

摘要

背景:神经丝光(NFL)在预后和治疗决策中越来越被认可。目的:验证脑脊液NFL (cNFL)作为复发-缓解型多发性硬化症(RRMS)生物标志物的临床应用价值。方法:回顾性分析2001-2018年在单一多发性硬化症(MS)学术中心进行cNFL分析的RRMS患者(n = 757),作为诊断检查的一部分。用两种不同的免疫测定法测定cNFL浓度,并使用它们之间的均值之比进行归一化。结果:复发的RRMS中位cNFL浓度(1134[四分位间距(IQR) 499 ~ 2744] ng/L)比未复发的RRMS中位cNFL浓度(264 [125 ~ 537]ng/L, p p p = 0.001, HR = 2.5, 95% CI = 1.4 ~ 4.2)高4.4倍。结论:cNFL是疾病活动性、治疗反应、预测残疾和从RRMS到SPMS转化的强大可靠的生物标志物。我们的数据表明,cNFL应包括在ms发病患者的评估中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study.

Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study.

Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study.

Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study.

Background: Neurofilament light (NFL) has been increasingly recognized for prognostic and therapeutic decisions.

Objective: To validate the utility of cerebrospinal fluid NFL (cNFL) as a biomarker in clinical practice of relapsing-remitting multiple sclerosis (RRMS).

Methods: RRMS patients (n = 757) who had cNFL analyzed as part of the diagnostic work-up in a single academic multiple sclerosis (MS) center, 2001-2018, were retrospectively identified. cNFL concentrations were determined with two different immunoassays and the ratio of means between them was used for normalization.

Results: RRMS with relapse had 4.4 times higher median cNFL concentration (1134 [interquartile range (IQR) 499-2744] ng/L) than those without relapse (264 [125-537] ng/L, p < 0.001) and patients with gadolinium-enhancing lesions had 3.3 times higher median NFL (1414 [606.8-3210] ng/L) than those without (426 [IQR 221-851] ng/L, p < 0.001). The sensitivity and specificity of cNFL to detect disease activity was 75% and 98.5%, respectively. High cNFL at MS onset predicted progression to Expanded Disability Status Scale (EDSS) ⩾ 3 (p < 0.001, hazard ratios (HR) = 1.89, 95% CI = 1.44-2.65) and conversion to secondary progressive MS (SPMS, p = 0.001, HR = 2.5, 95% CI = 1.4-4.2).

Conclusions: cNFL is a robust and reliable biomarker of disease activity, treatment response, and prediction of disability and conversion from RRMS to SPMS. Our data suggest that cNFL should be included in the assessment of patients at MS-onset.

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