• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Clinical Significance of Myelin Oligodendrocyte Glycoprotein Autoantibodies in Patients with Typical MS Lesions on MRI.髓鞘少突胶质细胞糖蛋白自身抗体在MRI上有典型MS病灶患者中的临床意义
Mult Scler J Exp Transl Clin. 2021 Nov 19;7(4):20552173211048761. doi: 10.1177/20552173211048761. eCollection 2021 Oct.
2
Progressive myelopathy in myelin oligodendrocyte glycoprotein antibody-associated disease: A new mimicker of progressive multiple sclerosis?髓鞘少突胶质细胞糖蛋白抗体相关性疾病中的进行性脊髓病:进展型多发性硬化症的新模拟者?
Mult Scler Relat Disord. 2021 Jul;52:102964. doi: 10.1016/j.msard.2021.102964. Epub 2021 Apr 20.
3
Clinical, Radiologic, and Prognostic Features of Myelitis Associated With Myelin Oligodendrocyte Glycoprotein Autoantibody.髓鞘少突胶质细胞糖蛋白自身抗体相关脊髓炎的临床、放射学和预后特征。
JAMA Neurol. 2019 Mar 1;76(3):301-309. doi: 10.1001/jamaneurol.2018.4053.
4
[Clinical characteristics of myelin oligodendrocyte glycoprotein antibody associated myelitis].髓鞘少突胶质细胞糖蛋白抗体相关脊髓炎的临床特征
Zhonghua Yi Xue Za Zhi. 2020 Feb 11;100(5):334-338. doi: 10.3760/cma.j.issn.0376-2491.2020.05.004.
5
Anti-MOG associated disorder-Clinical and radiological characteristics compared to AQP4-IgG+ NMOSD-A single-center experience.抗髓鞘少突胶质细胞糖蛋白相关疾病与水通道蛋白4-IgG阳性视神经脊髓炎谱系障碍的临床和影像学特征比较——单中心经验
Mult Scler Relat Disord. 2021 Feb;48:102718. doi: 10.1016/j.msard.2020.102718. Epub 2020 Dec 24.
6
Clinical and Imaging Features of Patients With Encephalitic Symptoms and Myelin Oligodendrocyte Glycoprotein Antibodies.脑炎症状和髓鞘少突胶质细胞糖蛋白抗体患者的临床和影像学特征。
Front Immunol. 2021 Oct 7;12:722404. doi: 10.3389/fimmu.2021.722404. eCollection 2021.
7
Comparison of MRI Lesion Evolution in Different Central Nervous System Demyelinating Disorders.不同中枢神经系统脱髓鞘疾病的 MRI 病变演变比较。
Neurology. 2021 Sep 14;97(11):e1097-e1109. doi: 10.1212/WNL.0000000000012467. Epub 2021 Jul 14.
8
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 2: Epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome.视神经脊髓炎及相关疾病中的髓鞘少突胶质细胞糖蛋白免疫球蛋白G:50例患者的多中心研究。第2部分:流行病学、临床表现、影像学和实验室特征、治疗反应及长期预后
J Neuroinflammation. 2016 Sep 27;13(1):280. doi: 10.1186/s12974-016-0718-0.
9
Chronic relapsing inflammatory optic neuropathy (CRION): a manifestation of myelin oligodendrocyte glycoprotein antibodies.慢性复发性炎症性视神经病变(CRION):髓鞘少突胶质细胞糖蛋白抗体的一种表现。
J Neuroinflammation. 2018 Oct 31;15(1):302. doi: 10.1186/s12974-018-1335-x.
10
Positive Predictive Value of Myelin Oligodendrocyte Glycoprotein Autoantibody Testing.髓鞘少突胶质细胞糖蛋白自身抗体检测的阳性预测值。
JAMA Neurol. 2021 Jun 1;78(6):741-746. doi: 10.1001/jamaneurol.2021.0912.

引用本文的文献

1
MOG Antibody Disease: Nuances in Presentation, Diagnosis, and Management.髓鞘少突胶质细胞糖蛋白抗体病:临床表现、诊断及治疗的细微差别
Curr Neurol Neurosci Rep. 2024 Aug;24(8):219-232. doi: 10.1007/s11910-024-01344-z. Epub 2024 May 28.
2
Alterations in Aquaporin-4-IgG Serostatus in 986 Patients: A Laboratory-Based Longitudinal Analysis.986 例患者水通道蛋白-4 免疫球蛋白 G 血清状态变化:基于实验室的纵向分析。
Ann Neurol. 2023 Oct;94(4):727-735. doi: 10.1002/ana.26722. Epub 2023 Jul 5.
3
Myelitis features and outcomes in CNS demyelinating disorders: Comparison between multiple sclerosis, MOGAD, and AQP4-IgG-positive NMOSD.中枢神经系统脱髓鞘疾病中的脊髓炎特征及转归:多发性硬化、MOG抗体相关疾病及水通道蛋白4-IgG阳性视神经脊髓炎谱系疾病的比较
Front Neurol. 2022 Nov 7;13:1011579. doi: 10.3389/fneur.2022.1011579. eCollection 2022.
4
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): A Review of Clinical and MRI Features, Diagnosis, and Management.髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD):临床与MRI特征、诊断及管理综述
Front Neurol. 2022 Jun 17;13:885218. doi: 10.3389/fneur.2022.885218. eCollection 2022.
5
Testing for Antibodies Against Aquaporin-4 and Myelin Oligodendrocyte Glycoprotein in the Diagnosis of Patients With Suspected Autoimmune Myelopathy.检测抗水通道蛋白4和髓鞘少突胶质细胞糖蛋白抗体在疑似自身免疫性脊髓病患者诊断中的应用
Front Neurol. 2022 May 20;13:912050. doi: 10.3389/fneur.2022.912050. eCollection 2022.

本文引用的文献

1
Frequency of myelin oligodendrocyte glycoprotein antibodies in a large cohort of neurological patients.一大群神经疾病患者中髓鞘少突胶质细胞糖蛋白抗体的频率
Mult Scler J Exp Transl Clin. 2021 Jun 25;7(2):20552173211022767. doi: 10.1177/20552173211022767. eCollection 2021 Apr-Jun.
2
Comparison of MRI Lesion Evolution in Different Central Nervous System Demyelinating Disorders.不同中枢神经系统脱髓鞘疾病的 MRI 病变演变比较。
Neurology. 2021 Sep 14;97(11):e1097-e1109. doi: 10.1212/WNL.0000000000012467. Epub 2021 Jul 14.
3
Positive Predictive Value of Myelin Oligodendrocyte Glycoprotein Autoantibody Testing.髓鞘少突胶质细胞糖蛋白自身抗体检测的阳性预测值。
JAMA Neurol. 2021 Jun 1;78(6):741-746. doi: 10.1001/jamaneurol.2021.0912.
4
Silent New Brain MRI Lesions in Children with MOG-Antibody Associated Disease.MOG 抗体相关性疾病患儿的脑 MRI 新 silent 病变。
Ann Neurol. 2021 Feb;89(2):408-413. doi: 10.1002/ana.25957. Epub 2020 Nov 30.
5
Long-term Outcomes in Patients With Myelin Oligodendrocyte Glycoprotein Immunoglobulin G-Associated Disorder.髓鞘少突胶质细胞糖蛋白免疫球蛋白 G 相关疾病患者的长期结局。
JAMA Neurol. 2020 Dec 1;77(12):1575-1577. doi: 10.1001/jamaneurol.2020.3115.
6
The frequency of longitudinally extensive transverse myelitis in MS: A population-based study.多发性硬化症中纵向广泛横贯性脊髓炎的频率:一项基于人群的研究。
Mult Scler Relat Disord. 2020 Jan;37:101487. doi: 10.1016/j.msard.2019.101487. Epub 2019 Oct 31.
7
Coexistence of Myelin Oligodendrocyte Glycoprotein and Aquaporin-4 Antibodies in Adult and Pediatric Patients.髓鞘少突胶质细胞糖蛋白和水通道蛋白-4 抗体在成年和儿科患者中的共存。
JAMA Neurol. 2020 Feb 1;77(2):257-259. doi: 10.1001/jamaneurol.2019.3656.
8
Assessment of lesions on magnetic resonance imaging in multiple sclerosis: practical guidelines.多发性硬化症磁共振成像病变评估:实用指南。
Brain. 2019 Jul 1;142(7):1858-1875. doi: 10.1093/brain/awz144.
9
MOG encephalomyelitis: international recommendations on diagnosis and antibody testing.MOG 脑炎:诊断和抗体检测的国际建议。
J Neuroinflammation. 2018 May 3;15(1):134. doi: 10.1186/s12974-018-1144-2.
10
Clinical spectrum and prognostic value of CNS MOG autoimmunity in adults: The MOGADOR study.成人中枢神经系统 MOG 自身免疫的临床谱和预后价值:MOGADOR 研究。
Neurology. 2018 May 22;90(21):e1858-e1869. doi: 10.1212/WNL.0000000000005560. Epub 2018 Apr 25.

髓鞘少突胶质细胞糖蛋白自身抗体在MRI上有典型MS病灶患者中的临床意义

Clinical Significance of Myelin Oligodendrocyte Glycoprotein Autoantibodies in Patients with Typical MS Lesions on MRI.

作者信息

Zara Pietro, Floris Valentina, Flanagan Eoin P, Lopez-Chiriboga A Sebastian, Weinshenker Brian G, Solla Paolo, Sechi Elia

机构信息

Department of Medical, Surgical and Experimental Sciences, University of Sassari - AOU Sassari, Sassari, Italy.

Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.

出版信息

Mult Scler J Exp Transl Clin. 2021 Nov 19;7(4):20552173211048761. doi: 10.1177/20552173211048761. eCollection 2021 Oct.

DOI:10.1177/20552173211048761
PMID:34820135
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8606934/
Abstract

BACKGROUND

Myelin-oligodendrocyte-glycoprotein (MOG)-IgG-positivity in patients with typical MS lesions on MRI may lead to diagnostic/therapeutic uncertainty.

OBJECTIVE AND METHODS

We reviewed reports of cases with MS phenotype on MRI and MOG-IgG-positivity published in Pubmed between 01/2012-06/2021.

RESULTS

Sixteen patients were included (median age [range], 37,5 [25-66] years; 60% female). Three patients initially tested negative for MOG-IgG. Disease course was: relapsing-remitting, 10; or progressive, 6. Intrathecal IgG-synthesis was common (79%). Low and high-efficacy MS-targeted agents prevented relapses in 30% and 100%, respectively. None of the patients showed resolution of MRI T2-lesions over time.

CONCLUSIONS

MOG-IgG-positivity is unlikely to alter the expected treatment response and outcomes in patients with otherwise typical MS phenotype on MRI.

摘要

背景

MRI显示典型多发性硬化(MS)病灶的患者中,髓鞘少突胶质细胞糖蛋白(MOG)-IgG阳性可能导致诊断/治疗的不确定性。

目的与方法

我们回顾了2012年1月至2021年6月期间发表在Pubmed上的MRI表现为MS表型且MOG-IgG阳性的病例报告。

结果

纳入16例患者(中位年龄[范围],37.5[25-66]岁;60%为女性)。3例患者最初MOG-IgG检测为阴性。病程为:复发缓解型,10例;或进展型,6例。鞘内IgG合成常见(79%)。低效能和高效能的MS靶向药物分别使30%和100%的患者预防了复发。随着时间推移,没有患者的MRI T2病灶消退。

结论

对于MRI表现为其他典型MS表型的患者,MOG-IgG阳性不太可能改变预期的治疗反应和结果。