• 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

视神经脊髓炎复发:种族和复发率、免疫抑制和损伤。

Neuromyelitis optica relapses: Race and rate, immunosuppression and impairment.

机构信息

Nuffield Department of Clinical Neurosciences, Oxford University, John Radcliffe Hospital, Oxford, UK.

Alexion Pharmaceutical, 55 Cambridge Parkway (Suite 800), Cambridge, MA 02142, USA.

出版信息

Mult Scler Relat Disord. 2016 May;7:21-5. doi: 10.1016/j.msard.2016.02.014. Epub 2016 Feb 16.

DOI:10.1016/j.msard.2016.02.014
PMID:27237752
Abstract

OBJECTIVE

Neuromyelitis optica (NMO) is a rare antibody-mediated CNS disease characterised by disabling relapses leading to high morbidity and mortality. Understanding relapse activity and severity is important for treatment decisions and clinical trial design. We assessed (1) whether clinical and demographic factors associate with different relapse rates and (2) the relative impact of immunosuppressive treatments on relapse rates and on attack-related residual disability.

METHODS

Clinical, demographic and treatment data were prospectively collected from 79 consecutive aquaporin 4 antibody positive patients seen in the nationally commissioned Oxford NMO service. The influence of clinical features on annualised relapse rates (using multiple regression) and the effect of immunosuppression on relapse-associated residual disability for transverse myelitis and optic neuritis attacks (using a mixed effect model) were analysed.

RESULTS

The mean annualised relapse rate was 0.93. Relapse rates were significantly higher in Afro-Caribbeans, children and in those of shorter disease duration. Relapse rates reduced on treatment (from 0.87 to 0.42). Delay to first treatment did not influence eventual on-treatment relapse rate. Immunosuppressive treatment significantly reduced the residual disability from ON (p<0.01), and TM (p=0.029) attacks.

CONCLUSIONS

Relapse rates in NMO are influenced by multiple factors, including age, ethnicity and disease duration. Current immunosuppressive treatments reduce but do not abolish relapses, however, they appear to additionally lessen the chronic disabling effect of a relapse.

摘要

目的

视神经脊髓炎(NMO)是一种罕见的以抗体介导的中枢神经系统疾病,其特征为致残性复发,导致高发病率和死亡率。了解复发活动和严重程度对于治疗决策和临床试验设计很重要。我们评估了(1)临床和人口统计学因素是否与不同的复发率相关,以及(2)免疫抑制治疗对复发率和与攻击相关的残留残疾的相对影响。

方法

从全国委托的牛津 NMO 服务中连续观察到的 79 例水通道蛋白 4 抗体阳性患者中前瞻性地收集了临床、人口统计学和治疗数据。使用多元回归分析了临床特征对年化复发率的影响,以及使用混合效应模型分析了免疫抑制对横贯性脊髓炎和视神经炎攻击相关残留残疾的影响。

结果

平均年化复发率为 0.93。非裔加勒比人、儿童和疾病持续时间较短的患者复发率明显较高。治疗后复发率降低(从 0.87 降至 0.42)。首次治疗的延迟并未影响最终治疗中的复发率。免疫抑制治疗显著降低了 ON(p<0.01)和 TM(p=0.029)攻击的残留残疾。

结论

NMO 的复发率受到多种因素的影响,包括年龄、种族和疾病持续时间。目前的免疫抑制治疗可减少复发,但不能完全消除复发,然而,它们似乎还可以减轻复发的慢性致残影响。

相似文献

1
Neuromyelitis optica relapses: Race and rate, immunosuppression and impairment.视神经脊髓炎复发:种族和复发率、免疫抑制和损伤。
Mult Scler Relat Disord. 2016 May;7:21-5. doi: 10.1016/j.msard.2016.02.014. Epub 2016 Feb 16.
2
Methotrexate is an alternative to azathioprine in neuromyelitis optica spectrum disorders with aquaporin-4 antibodies.甲氨蝶呤是视神经脊髓炎谱系疾病伴水通道蛋白 4 抗体患者的硫唑嘌呤替代药物。
J Neurol Neurosurg Psychiatry. 2013 Aug;84(8):918-21. doi: 10.1136/jnnp-2012-304774. Epub 2013 Mar 6.
3
Evaluation of effect of empirical attack-preventive immunotherapies in neuromyelitis optica spectrum disorders: An update systematic review and meta -analysis.视神经脊髓炎谱系疾病经验性预防治疗效果评估:一项更新的系统评价和荟萃分析。
J Neuroimmunol. 2022 Feb 15;363:577790. doi: 10.1016/j.jneuroim.2021.577790. Epub 2021 Dec 16.
4
Clinical characteristics of disabling attacks at onset in patients with neuromyelitis optica spectrum disorder.视神经脊髓炎谱系障碍患者起病时致残性发作的临床特征
J Neurol Sci. 2016 Sep 15;368:209-13. doi: 10.1016/j.jns.2016.06.030. Epub 2016 Jun 14.
5
Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders.AQP4-IgG 阳性视神经脊髓炎谱系疾病的预后预测模型。
Brain. 2019 May 1;142(5):1310-1323. doi: 10.1093/brain/awz054.
6
Devic's neuromyelitis optica: clinical features and prognostic factors.视神经脊髓炎谱系疾病:临床特征与预后因素
Neurol Sci. 2004 Nov;25 Suppl 4:S364-7. doi: 10.1007/s10072-004-0342-0.
7
Effectiveness of rituximab versus oral immunosuppressive therapies in neuromyelitis optica spectrum disorder in a racially diverse cohort of subjects: A single-center retrospective study.利妥昔单抗与口服免疫抑制疗法在种族多样化的视神经脊髓炎谱系疾病患者中的疗效比较:一项单中心回顾性研究。
Mult Scler Relat Disord. 2023 Jun;74:104718. doi: 10.1016/j.msard.2023.104718. Epub 2023 Apr 16.
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
Patterns of neuromyelitis optica spectrum disorder attacks in different age groups and sexes depending on the status of immunosuppressive therapy: A retrospective cohort study.基于免疫抑制治疗状况的不同年龄组和性别之间视神经脊髓炎谱系疾病发作模式:一项回顾性队列研究。
Eur J Neurol. 2024 Mar;31(3):e16178. doi: 10.1111/ene.16178. Epub 2023 Dec 20.
10
Effectiveness of treatments in Neuromyelitis optica to modify the course of disease in adult patients. Systematic review of literature.治疗视神经脊髓炎以改变成年患者病程的有效性。文献系统评价。
Mult Scler Relat Disord. 2021 May;50:102869. doi: 10.1016/j.msard.2021.102869. Epub 2021 Feb 25.

引用本文的文献

1
Impact of neuromyelitis optica spectrum disorder on employment and income in the United States.视神经脊髓炎谱系疾病对美国就业和收入的影响。
Ann Clin Transl Neurol. 2024 Apr;11(4):1011-1020. doi: 10.1002/acn3.52021. Epub 2024 Feb 20.
2
Understanding the employment impact of neuromyelitis optica spectrum disorder in the USA: Mixed methods.了解视神经脊髓炎谱系障碍对美国就业的影响:混合研究方法。
Front Neurol. 2023 Mar 9;14:1142640. doi: 10.3389/fneur.2023.1142640. eCollection 2023.
3
Assessing attacks and treatment response rates among adult patients with NMOSD and MOGAD: Data from a nationwide registry in Argentina.
评估成年视神经脊髓炎谱系障碍(NMOSD)和髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)患者的发作情况及治疗反应率:来自阿根廷全国登记处的数据
Mult Scler J Exp Transl Clin. 2021 Aug 20;7(3):20552173211032334. doi: 10.1177/20552173211032334. eCollection 2021 Jul-Sep.
4
Comparison of Clinical Outcomes of Transverse Myelitis Among Adults With Myelin Oligodendrocyte Glycoprotein Antibody vs Aquaporin-4 Antibody Disease.成人髓鞘少突胶质细胞糖蛋白抗体与水通道蛋白 4 抗体疾病的横断性脊髓炎临床结局比较。
JAMA Netw Open. 2019 Oct 2;2(10):e1912732. doi: 10.1001/jamanetworkopen.2019.12732.
5
Collaborative International Research in Clinical and Longitudinal Experience Study in NMOSD.视神经脊髓炎临床与纵向经验研究的国际合作研究。
Neurol Neuroimmunol Neuroinflamm. 2019 Jun 28;6(5):e583. doi: 10.1212/NXI.0000000000000583. eCollection 2019 Sep.
6
Diagnosis and Treatment of NMO Spectrum Disorder and MOG-Encephalomyelitis.视神经脊髓炎谱系障碍和髓鞘少突胶质细胞糖蛋白脑病的诊断与治疗
Front Neurol. 2018 Oct 23;9:888. doi: 10.3389/fneur.2018.00888. eCollection 2018.
7
Use of Rituximab and Risk of Re-hospitalization for Children with Neuromyelitis Optica Spectrum Disorder.利妥昔单抗的使用与视神经脊髓炎谱系障碍儿童再次住院的风险
Mult Scler Demyelinating Disord. 2018 Apr;3. doi: 10.1186/s40893-018-0035-9. Epub 2018 Apr 17.
8
Dose effects of mycophenolate mofetil in Chinese patients with neuromyelitis optica spectrum disorders: a case series study.霉酚酸酯对中国视神经脊髓炎谱系障碍患者的剂量效应:一项病例系列研究。
BMC Neurol. 2018 Apr 23;18(1):47. doi: 10.1186/s12883-018-1056-x.
9
Practice current: How do you treat neuromyelitis optica?临床实践:你如何治疗视神经脊髓炎?
Neurol Clin Pract. 2017 Apr;7(2):170-178. doi: 10.1212/CPJ.0000000000000352.
10
Immunotherapies in neuromyelitis optica spectrum disorder: efficacy and predictors of response.视神经脊髓炎谱系障碍中的免疫疗法:疗效及反应预测因素
J Neurol Neurosurg Psychiatry. 2017 Aug;88(8):639-647. doi: 10.1136/jnnp-2017-315603. Epub 2017 Jun 1.