MOG抗体相关疾病中无攻击性非依赖性神经轴突损伤:血清神经丝轻链的纵向评估。

Jae-Won Hyun, So Yeon Kim, Yeseul Kim, Na Young Park, Ki Hoon Kim, Su-Hyun Kim, Ho Jin Kim
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引用次数: 1

摘要

为了评估髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)中发作无关的神经轴突和星形细胞损伤的发生,使用单分子阵列法纵向测量102例血清神经丝轻链(sNfL)和血清胶质纤维酸性蛋白(sGFAP)水平。本研究分析了15名复发性MOGAD成人的血清和26名年龄/性别匹配的健康对照。sNfL水平在所有临床发作中均显著升高,在发作后6个月内降至临界值以下或接近临界值。在两次发作期间,sNfL水平一直很低。相反,sGFAP水平在大多数临床发作中没有增加,并且在随访期间保持在较低水平。临床发作时观察到明显的神经轴突损伤,而在MOGAD中没有发作无关的神经轴突和星形细胞损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absence of attack-independent neuroaxonal injury in MOG antibody-associated disease: Longitudinal assessment of serum neurofilament light chain.

To evaluate the occurrence of attack-independent neuroaxonal and astrocytic damage in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), serum neurofilament light chain (sNfL) and serum glial fibrillary acidic protein (sGFAP) levels were longitudinally measured in 102 sera using a single-molecule array assay. Sera from 15 adults with relapsing MOGAD with available longitudinal samples for the median 24-month follow-up and 26 age-/sex-matched healthy controls were analyzed. sNfL levels were significantly elevated in all clinical attacks, where the levels decreased below or close to cut-off value within 6 months after attacks. sNfL levels were consistently low during inter-attack periods. In contrast, sGFAP levels did not increase in most clinical attacks and remained low during follow-up. Significant neuroaxonal damage was observed at clinical attacks, while attack-independent neuroaxonal and astrocytic injury was absent in MOGAD.

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