Body fluid markers for multiple sclerosis and differential diagnosis from atypical demyelinating disorders

被引:0
|
作者
Bauer, Angelika [1 ,2 ]
Hegen, Harald [1 ]
Reindl, Markus [1 ]
机构
[1] Med Univ Innsbruck, Clin Dept Neurol, Innsbruck, Austria
[2] Med Univ Innsbruck, Inst Hyg & Med Microbiol, Innsbruck, Austria
关键词
Biomarker; clinically isolated syndrome; demyelinating disorder; first demyelinating CNS event; multiple sclerosis; myelin oligodendrocyte glycoprotein associated disease; neuromyelitis optica spectrum disorder; oligoclonal bands; CLINICALLY ISOLATED SYNDROME; EPSTEIN-BARR-VIRUS; MYELIN OLIGODENDROCYTE GLYCOPROTEIN; NEUROFILAMENT LIGHT-CHAIN; CHITINASE; 3-LIKE; RECTIFYING POTASSIUM CHANNELS; CEREBROSPINAL-FLUID; NEUROMYELITIS-OPTICA; ANTIMYELIN ANTIBODIES; DISEASE-ACTIVITY;
D O I
10.1080/14737159.2024.2334849
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
IntroductionBody fluid markers could be helpful to predict the conversion into clinically definite multiple sclerosis (MS) in people with a first demyelinating event of the central nervous system (CNS). Consequently, biomarkers such as oligoclonal bands, which are integrated in the current MS diagnostic criteria, could assist early MS diagnosis.Areas coveredThis review examines existing knowledge on a broad spectrum of body fluid markers in people with a first CNS demyelinating event, explores their potential to predict conversion to MS, to assess MS disease activity, as well as their utility to differentiate MS from atypical demyelinating disorders such as neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein associated disease.Expert opinionThis field of research has shown a dramatic increase of evidence, especially in the last decade. Some biomarkers are already established in clinical routine (e.g. oligoclonal bands) while others are currently implemented (e.g. kappa free light chains) or considered as breakthroughs (e.g. neurofilament light). Determination of biomarkers poses challenges for continuous monitoring, especially if exclusively detectable in cerebrospinal fluid. A handful of biomarkers are measurable in blood which holds a significant potential.
引用
收藏
页码:283 / 297
页数:15
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