多发性硬化
医学
生物标志物
亚临床感染
磁共振成像
疾病
脑脊液
病理
肿瘤科
放射科
免疫学
生物化学
化学
作者
Mark S. Freedman,Sharmilee Gnanapavan,Ronald A. Booth,Peter A. Calabresi,Michael Khalil,Jens Kühle,Jan Lycke,Tomas Olsson
出处
期刊:EBioMedicine
[Elsevier BV]
日期:2024-02-13
卷期号:101: 104970-104970
被引量:76
标识
DOI:10.1016/j.ebiom.2024.104970
摘要
Neurofilament light chain (NfL) is a long-awaited blood biomarker that can provide clinically useful information about prognosis and therapeutic efficacy in multiple sclerosis (MS). There is now substantial evidence for this biomarker to be used alongside magnetic resonance imaging (MRI) and clinical measures of disease progression as a decision-making tool for the management of patients with MS. Serum NfL (sNfL) has certain advantages over traditional measures of MS disease progression such as MRI because it is relatively noninvasive, inexpensive, and can be repeated frequently to monitor activity and treatment efficacy. sNfL levels can be monitored regularly in patients with MS to determine change from baseline and predict subclinical disease activity, relapse risk, and the development of gadolinium-enhancing (Gd+) lesions. sNfL does not replace MRI, which provides information related to spatial localisation and lesion stage. Laboratory platforms are starting to be made available for clinical application of sNfL in several countries. Further work is needed to resolve issues around comparisons across testing platforms (absolute values) and normalisation (reference ranges) in order to guide interpretation of the results.
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