Clinical, imaging, and immunotherapeutic features in MOGAD: a retrospective real-world cohort in Northern China.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Therapeutic Advances in Neurological Disorders Pub Date : 2026-06-29 eCollection Date: 2026-01-01 DOI:10.1177/17562864261458528
Xuetao Cao, Danqing Qin, Chunjuan Wang, Baojie Wang, Yuxiu Xiao, Xujun Chu, Shougang Guo
{"title":"Clinical, imaging, and immunotherapeutic features in MOGAD: a retrospective real-world cohort in Northern China.","authors":"Xuetao Cao, Danqing Qin, Chunjuan Wang, Baojie Wang, Yuxiu Xiao, Xujun Chu, Shougang Guo","doi":"10.1177/17562864261458528","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a clinically heterogeneous demyelinating disorder. Current knowledge of its phenotypic spectrum and optimal treatment strategies, especially in Asian populations, remains limited.</p><p><strong>Objectives: </strong>This study aimed to characterize the clinical and imaging features of MOGAD in a Northern Chinese cohort and to evaluate the therapeutic effects of the anti-CD20 monoclonal antibody ofatumumab.</p><p><strong>Design: </strong>A retrospective study in a single center.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of 108 patients who tested positive for MOG antibodies between June 2018 and August 2025, ultimately diagnosing 56 patients with MOGAD comprising 17 pediatric and 39 adult cases. Clinical, imaging, and cerebrospinal fluid (CSF) data were systematically reviewed. Ten patients received ofatumumab treatment for relapse prevention. The study was approved by the Ethics Committee of Shandong Provincial Hospital Affiliated to Shandong First Medical University (SWYX: NO.2025-709) and written consent was obtained from all participants.</p><p><strong>Results: </strong>Cortical encephalitis was the most frequent phenotype (41.1%, 23/56), followed by Unifocal Demyelination (39.3%, 22/56). Radiographically, 94.4% of patients exhibited 1-3 lesions, predominantly in cortical regions. CSF analysis revealed elevated cell counts and protein levels, with significant variation across phenotypes (<i>p</i> < 0.05). Adults with relapsing courses experienced greater disability progression (<i>p</i> = 0.006). Ofatumumab treatment resulted in no observed relapses, along with improvements in Expanded Disability Status Scale (EDSS) and modified Rankin Scale (mRS) scores and reduction in MRI lesion burden compared with baseline (all <i>p</i> < 0.05). Notably, 50% (5/10) of ofatumumab-treated patients discontinued glucocorticoids within 12 months, compared with 19.6% (9/46) in the conventional therapy group (<i>p</i> = 0.017).</p><p><strong>Conclusion: </strong>This study delineates a distinct clinical-radiological profile of MOGAD in Northern China, characterized by a high frequency of cortical encephalitis. Furthermore, it provides preliminary evidence that ofatumumab may be a potential steroid-sparing therapeutic option for MOGAD.</p>","PeriodicalId":22980,"journal":{"name":"Therapeutic Advances in Neurological Disorders","volume":"19 ","pages":"17562864261458528"},"PeriodicalIF":4.0000,"publicationDate":"2026-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13319572/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Advances in Neurological Disorders","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/17562864261458528","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a clinically heterogeneous demyelinating disorder. Current knowledge of its phenotypic spectrum and optimal treatment strategies, especially in Asian populations, remains limited.

Objectives: This study aimed to characterize the clinical and imaging features of MOGAD in a Northern Chinese cohort and to evaluate the therapeutic effects of the anti-CD20 monoclonal antibody ofatumumab.

Design: A retrospective study in a single center.

Methods: We conducted a retrospective analysis of 108 patients who tested positive for MOG antibodies between June 2018 and August 2025, ultimately diagnosing 56 patients with MOGAD comprising 17 pediatric and 39 adult cases. Clinical, imaging, and cerebrospinal fluid (CSF) data were systematically reviewed. Ten patients received ofatumumab treatment for relapse prevention. The study was approved by the Ethics Committee of Shandong Provincial Hospital Affiliated to Shandong First Medical University (SWYX: NO.2025-709) and written consent was obtained from all participants.

Results: Cortical encephalitis was the most frequent phenotype (41.1%, 23/56), followed by Unifocal Demyelination (39.3%, 22/56). Radiographically, 94.4% of patients exhibited 1-3 lesions, predominantly in cortical regions. CSF analysis revealed elevated cell counts and protein levels, with significant variation across phenotypes (p < 0.05). Adults with relapsing courses experienced greater disability progression (p = 0.006). Ofatumumab treatment resulted in no observed relapses, along with improvements in Expanded Disability Status Scale (EDSS) and modified Rankin Scale (mRS) scores and reduction in MRI lesion burden compared with baseline (all p < 0.05). Notably, 50% (5/10) of ofatumumab-treated patients discontinued glucocorticoids within 12 months, compared with 19.6% (9/46) in the conventional therapy group (p = 0.017).

Conclusion: This study delineates a distinct clinical-radiological profile of MOGAD in Northern China, characterized by a high frequency of cortical encephalitis. Furthermore, it provides preliminary evidence that ofatumumab may be a potential steroid-sparing therapeutic option for MOGAD.

MOGAD的临床、影像学和免疫治疗特征:中国北方的回顾性现实世界队列。
背景:髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)是一种临床异质性脱髓鞘疾病。目前对其表型谱和最佳治疗策略的了解仍然有限,特别是在亚洲人群中。目的:本研究旨在描述中国北方队列中MOGAD的临床和影像学特征,并评估抗cd20单克隆抗体atumumab的治疗效果。设计:单中心回顾性研究。方法:对2018年6月至2025年8月期间MOG抗体检测呈阳性的108例患者进行回顾性分析,最终诊断为56例MOGAD患者,包括17例儿童和39例成人。临床,影像学和脑脊液(CSF)的数据进行了系统的审查。10例患者接受了ofatumumab治疗以预防复发。本研究已获得山东第一医科大学附属山东省医院伦理委员会批准(SWYX: NO.2025-709),并获得所有参与者的书面同意。结果:皮质性脑炎是最常见的表型(41.1%,23/56),其次是单灶性脱髓鞘(39.3%,22/56)。x线摄影显示,94.4%的患者表现为1-3个病变,主要在皮质区。脑脊液分析显示细胞计数和蛋白水平升高,不同表型之间存在显著差异(p p = 0.006)。与基线相比,Ofatumumab治疗没有观察到复发,同时扩展残疾状态量表(EDSS)和修改的Rankin量表(mRS)评分得到改善,MRI病变负担减轻(所有p p = 0.017)。结论:本研究描述了中国北方地区MOGAD的独特临床-放射学特征,其特征是高频率的皮质性脑炎。此外,它提供了初步证据,表明ofatumumab可能是一种潜在的不使用类固醇治疗MOGAD的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
8.30
自引率
1.70%
发文量
62
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Neurological Disorders is a peer-reviewed, open access journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of neurology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in neurology, providing a forum in print and online for publishing the highest quality articles in this area.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书