医学
多发性硬化
髓鞘少突胶质细胞糖蛋白
急性播散性脑脊髓炎
临床孤立综合征
脑脊髓炎
磁共振成像
生物标志物
病理
脊髓炎
胃肠病学
麦当劳标准
内科学
免疫学
脊髓
实验性自身免疫性脑脊髓炎
放射科
生物化学
化学
精神科
作者
Eva‐Maria Wendel,Annikki Bertolini,Lampros Kousoulos,Markus Rauchenzauner,Kathrin Schanda,Andreas Wegener-Panzer,Matthias Baumann,Markus Reindl,Markus Otto,Kevin Rostásy
标识
DOI:10.1177/13524585221081090
摘要
OBJECTIVE: To assess the diagnostic and prognostic potential of serum neurofilament light chain (sNfL) in children with first acquired demyelinating syndrome (ADS). METHODS: We selected 129 children with first ADS including 19 children with myelin oligodendrocyte glycoprotein (MOG)-antibody associated disease (MOGAD), 36 MOG/AQP4-seronegative ADS, and 74 with multiple sclerosis (MS) from the BIOMARKER study cohort. All children had a complete set of clinical, radiological, laboratory data and serum for NfL measurement using a highly sensitive digital ELISA (SIMOA). A control group of 35 children with non-inflammatory neurological diseases was included. sNfL levels were compared across patient groups according to clinical, laboratory, neuroradiological features and outcome after 2 years. RESULTS: < 0.05). CONCLUSION: sNfL levels are significantly elevated in all three studied pediatric ADS subtypes indicating neuroaxonal injury. In pediatric MS high levels of sNfL are associated with risk factors for disease progression.
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