髓鞘少突胶质细胞糖蛋白抗体相关疾病患者停止免疫抑制治疗的结果

IF 5 2区 医学 Q1 CLINICAL NEUROLOGY
Multiple Sclerosis Journal Pub Date : 2025-08-01 Epub Date: 2025-04-28 DOI:10.1177/13524585251320046
You-Ri Kang, Hyunjin Ju, Ki Hoon Kim, Seung Ho Choo, Woohee Ju, Sung-Min Kim, Sooyoung Kim, Eunhee Sohn, Tai-Seung Nam, Sun-Young Oh, Byeol-A Yoon, Jong Kuk Kim, Hyunjin Kim, Eun-Jae Lee, Young-Min Lim, Young Nam Kwon, Seung Woo Kim, Ha Young Shin, Jee-Eun Kim, In Soo Joo, Minsu Park, Hyung-Soo Lee, Byung-Jo Kim, Jin-Woo Park, Suk Yoon Lee, Woojun Kim, Jae-Won Hyun, Su-Hyun Kim, Ju-Hong Min, Ho Jin Kim
{"title":"髓鞘少突胶质细胞糖蛋白抗体相关疾病患者停止免疫抑制治疗的结果","authors":"You-Ri Kang, Hyunjin Ju, Ki Hoon Kim, Seung Ho Choo, Woohee Ju, Sung-Min Kim, Sooyoung Kim, Eunhee Sohn, Tai-Seung Nam, Sun-Young Oh, Byeol-A Yoon, Jong Kuk Kim, Hyunjin Kim, Eun-Jae Lee, Young-Min Lim, Young Nam Kwon, Seung Woo Kim, Ha Young Shin, Jee-Eun Kim, In Soo Joo, Minsu Park, Hyung-Soo Lee, Byung-Jo Kim, Jin-Woo Park, Suk Yoon Lee, Woojun Kim, Jae-Won Hyun, Su-Hyun Kim, Ju-Hong Min, Ho Jin Kim","doi":"10.1177/13524585251320046","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Research on the optimal duration of immunosuppressive therapy (IST) and the outcome upon its discontinuation in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) remains limited.</p><p><strong>Objective: </strong>To evaluate the outcomes following IST discontinuation in MOGAD.</p><p><strong>Methods: </strong>This multicenter retrospective study collected data from 333 MOGAD patients in Korea. Among 273 patients who received IST, 41 who discontinued IST were analyzed.</p><p><strong>Results: </strong>The median age at disease onset was 38.3 years (interquartile range (IQR), 27.6-53.1). Before IST withdrawal, 21 (51%) patients exhibited relapsing courses. Over a median follow-up of 23.5 months (IQR, 12.1-39.5) after discontinuation, 10 patients (24.4%) relapsed after a median of 8.2 months (IQR, 6.3-11.5). All relapses occurred in patients with a prior relapsing course (10/21, 47.6%); none with prior monophasic courses relapsed. Among 21 prior relapsing patients, relapse after discontinuation group had a shorter IST duration than non-relapse group (median, 9.4 vs 50.9 months, <i>p</i> = 0.036). None of the 41 patients had severe disability (Expanded Disability Status Scale (EDSS) score ⩾ 4.0 or Visual Functional System score ⩾ 5) at the last visit.</p><p><strong>Conclusion: </strong>IST discontinuation did not necessarily lead to relapse and could be considered with an individualized approach based on factors such as disease course and IST duration.</p>","PeriodicalId":18874,"journal":{"name":"Multiple Sclerosis Journal","volume":" ","pages":"1102-1109"},"PeriodicalIF":5.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Outcomes of immunosuppressive therapy discontinuation in patients with myelin oligodendrocyte glycoprotein antibody-associated disease.\",\"authors\":\"You-Ri Kang, Hyunjin Ju, Ki Hoon Kim, Seung Ho Choo, Woohee Ju, Sung-Min Kim, Sooyoung Kim, Eunhee Sohn, Tai-Seung Nam, Sun-Young Oh, Byeol-A Yoon, Jong Kuk Kim, Hyunjin Kim, Eun-Jae Lee, Young-Min Lim, Young Nam Kwon, Seung Woo Kim, Ha Young Shin, Jee-Eun Kim, In Soo Joo, Minsu Park, Hyung-Soo Lee, Byung-Jo Kim, Jin-Woo Park, Suk Yoon Lee, Woojun Kim, Jae-Won Hyun, Su-Hyun Kim, Ju-Hong Min, Ho Jin Kim\",\"doi\":\"10.1177/13524585251320046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Research on the optimal duration of immunosuppressive therapy (IST) and the outcome upon its discontinuation in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) remains limited.</p><p><strong>Objective: </strong>To evaluate the outcomes following IST discontinuation in MOGAD.</p><p><strong>Methods: </strong>This multicenter retrospective study collected data from 333 MOGAD patients in Korea. Among 273 patients who received IST, 41 who discontinued IST were analyzed.</p><p><strong>Results: </strong>The median age at disease onset was 38.3 years (interquartile range (IQR), 27.6-53.1). Before IST withdrawal, 21 (51%) patients exhibited relapsing courses. Over a median follow-up of 23.5 months (IQR, 12.1-39.5) after discontinuation, 10 patients (24.4%) relapsed after a median of 8.2 months (IQR, 6.3-11.5). All relapses occurred in patients with a prior relapsing course (10/21, 47.6%); none with prior monophasic courses relapsed. Among 21 prior relapsing patients, relapse after discontinuation group had a shorter IST duration than non-relapse group (median, 9.4 vs 50.9 months, <i>p</i> = 0.036). None of the 41 patients had severe disability (Expanded Disability Status Scale (EDSS) score ⩾ 4.0 or Visual Functional System score ⩾ 5) at the last visit.</p><p><strong>Conclusion: </strong>IST discontinuation did not necessarily lead to relapse and could be considered with an individualized approach based on factors such as disease course and IST duration.</p>\",\"PeriodicalId\":18874,\"journal\":{\"name\":\"Multiple Sclerosis Journal\",\"volume\":\" \",\"pages\":\"1102-1109\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Multiple Sclerosis Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/13524585251320046\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/28 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Multiple Sclerosis Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/13524585251320046","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:关于髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)的免疫抑制治疗(IST)的最佳持续时间和停药后的结果的研究仍然有限。目的:评价MOGAD患者停服IST后的预后。方法:这项多中心回顾性研究收集了韩国333例MOGAD患者的数据。在273例接受IST治疗的患者中,41例停止了IST治疗。结果:中位发病年龄为38.3岁(四分位间距(IQR), 27.6-53.1)。停药前,21例(51%)患者出现复发。停药后中位随访23.5个月(IQR, 12.1-39.5), 10例患者(24.4%)在中位随访8.2个月(IQR, 6.3-11.5)后复发。所有复发均发生在既往有复发过程的患者中(10/21,47.6%);既往单相病程无复发。21例既往复发患者中,停药后复发组IST持续时间短于非复发组(中位,9.4个月vs 50.9个月,p = 0.036)。41名患者在最后一次访问时都没有严重残疾(扩展残疾状态量表(EDSS)评分大于或等于4.0或视觉功能系统评分大于或等于5)。结论:停药并不一定会导致复发,可以根据病程和停药时间等因素进行个体化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes of immunosuppressive therapy discontinuation in patients with myelin oligodendrocyte glycoprotein antibody-associated disease.

Background: Research on the optimal duration of immunosuppressive therapy (IST) and the outcome upon its discontinuation in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) remains limited.

Objective: To evaluate the outcomes following IST discontinuation in MOGAD.

Methods: This multicenter retrospective study collected data from 333 MOGAD patients in Korea. Among 273 patients who received IST, 41 who discontinued IST were analyzed.

Results: The median age at disease onset was 38.3 years (interquartile range (IQR), 27.6-53.1). Before IST withdrawal, 21 (51%) patients exhibited relapsing courses. Over a median follow-up of 23.5 months (IQR, 12.1-39.5) after discontinuation, 10 patients (24.4%) relapsed after a median of 8.2 months (IQR, 6.3-11.5). All relapses occurred in patients with a prior relapsing course (10/21, 47.6%); none with prior monophasic courses relapsed. Among 21 prior relapsing patients, relapse after discontinuation group had a shorter IST duration than non-relapse group (median, 9.4 vs 50.9 months, p = 0.036). None of the 41 patients had severe disability (Expanded Disability Status Scale (EDSS) score ⩾ 4.0 or Visual Functional System score ⩾ 5) at the last visit.

Conclusion: IST discontinuation did not necessarily lead to relapse and could be considered with an individualized approach based on factors such as disease course and IST duration.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Multiple Sclerosis Journal
Multiple Sclerosis Journal 医学-临床神经学
CiteScore
10.90
自引率
6.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Multiple Sclerosis Journal is a peer-reviewed international journal that focuses on all aspects of multiple sclerosis, neuromyelitis optica and other related autoimmune diseases of the central nervous system. The journal for your research in the following areas: * __Biologic basis:__ pathology, myelin biology, pathophysiology of the blood/brain barrier, axo-glial pathobiology, remyelination, virology and microbiome, immunology, proteomics * __Epidemology and genetics:__ genetics epigenetics, epidemiology * __Clinical and Neuroimaging:__ clinical neurology, biomarkers, neuroimaging and clinical outcome measures * __Therapeutics and rehabilitation:__ therapeutics, rehabilitation, psychology, neuroplasticity, neuroprotection, and systematic management Print ISSN: 1352-4585
×
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