• 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

原发性进行性多发性硬化症中病变增强随时间而减弱。

Lesion enhancement diminishes with time in primary progressive multiple sclerosis.

机构信息

Department of Brain Repair and Rehabilitation, Institute of Neurology, University College London, London WC1N 3BG, UK.

出版信息

Mult Scler. 2010 Mar;16(3):317-24. doi: 10.1177/1352458509358090.

DOI:10.1177/1352458509358090
PMID:20203148
Abstract

Fewer gadolinium-enhancing lesions are seen in established primary progressive multiple sclerosis (PPMS) compared with other subtypes. Previously, we found unexpectedly high enhancement levels in early PPMS (42%), suggesting an early inflammatory phase. The objective of this study was to investigate whether this level of enhancement was maintained, and whether it influenced clinical progression, over 5 years. Forty-five patients with PPMS, within 5 years of onset, were scored on the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Functional Composite (MSFC) and its subtests (including the timed walk test [TWT]) 6-monthly for 3 years, and at 5 years. T1-weighted brain and spinal cord images after triple dose gadolinium-DTPA, and T2-weighted brain sequences were also acquired. A mixed effect logistic model evaluated change in the percentage of patients with enhancing lesions. Ordinal logistic and multiple linear regression models identified predictors of progression, adjusted for T2 lesion load. The percentage of patients with enhancing lesions in the brain and spinal cord declined over 5 years (p = 0.03). Among patients with enhancement, more enhancing lesions at baseline predicted greater decline in mobility on the TWT over 5 years (p = 0.02). In conclusion, a proportion of patients with PPMS may undergo an early inflammatory phase, which has some impact on subsequent mobility.

摘要

与其他亚型相比,在已确诊的原发性进展型多发性硬化症(PPMS)中,增强病变的数量较少。此前,我们发现早期 PPMS 中增强水平出乎意料地高(42%),这表明存在早期炎症期。本研究的目的是调查这种增强水平是否持续存在,以及它是否会影响 5 年内的临床进展。45 名发病后 5 年内的 PPMS 患者,每隔 6 个月接受一次扩展残疾状态量表(EDSS)、多发性硬化功能综合量表(MSFC)及其子测试(包括定时步行测试[TWT])评分,持续 3 年,第 5 年再评分一次。在 3 年内,还获得了 T1 加权脑和脊髓图像,使用三重剂量钆-DTPA 增强,以及 T2 加权脑序列。混合效应逻辑模型评估了增强病变患者比例的变化。有序逻辑和多元线性回归模型确定了进展的预测因素,调整了 T2 病变负荷。脑和脊髓增强病变的患者比例在 5 年内下降(p=0.03)。在有增强的患者中,基线时更多的增强病变预示着 TWT 上移动能力在 5 年内下降更大(p=0.02)。总之,一部分 PPMS 患者可能经历早期炎症期,这对随后的移动能力有一定影响。

相似文献

1
Lesion enhancement diminishes with time in primary progressive multiple sclerosis.原发性进行性多发性硬化症中病变增强随时间而减弱。
Mult Scler. 2010 Mar;16(3):317-24. doi: 10.1177/1352458509358090.
2
Responsiveness and predictive value of EDSS and MSFC in primary progressive MS.扩展残疾状态量表(EDSS)和多发性硬化功能综合评分(MSFC)在原发性进行性多发性硬化中的反应性和预测价值。
Neurology. 2008 Mar 25;70(13 Pt 2):1084-91. doi: 10.1212/01.wnl.0000288179.86056.e1. Epub 2008 Jan 9.
3
Evolution of T1 black holes in patients with multiple sclerosis imaged monthly for 4 years.对患有多发性硬化症的患者的T1黑洞进行4年每月一次成像的演变情况。
Brain. 2003 Aug;126(Pt 8):1782-9. doi: 10.1093/brain/awg182. Epub 2003 Jun 23.
4
Cortical lesions in primary progressive multiple sclerosis: a 2-year longitudinal MR study.原发性进行性多发性硬化症的皮质病变:一项为期2年的纵向磁共振研究。
Neurology. 2009 Apr 14;72(15):1330-6. doi: 10.1212/WNL.0b013e3181a0fee5.
5
Grey matter damage predicts the evolution of primary progressive multiple sclerosis at 5 years.灰质损伤可预测原发性进行性多发性硬化症5年的病情进展。
Brain. 2006 Oct;129(Pt 10):2628-34. doi: 10.1093/brain/awl222. Epub 2006 Aug 18.
6
Voxel-based assessment of differences in damage and distribution of white matter lesions between patients with primary progressive and relapsing-remitting multiple sclerosis.基于体素的原发性进行性和复发缓解型多发性硬化症患者白质病变损伤及分布差异评估
Arch Neurol. 2008 Feb;65(2):236-43. doi: 10.1001/archneurol.2007.51.
7
ADC measurements in various patterns of multiple sclerosis lesions.多发性硬化症病变不同模式下的表观扩散系数测量
J Med Assoc Thai. 2006 Feb;89(2):196-204.
8
Increased plasma 8,12-iso-iPF2alpha- VI levels in relapsing multiple sclerosis patients are not predictive of disease progression.复发型多发性硬化症患者血浆 8,12-iso-iPF2alpha-VI 水平升高与疾病进展无关。
Mult Scler. 2012 Aug;18(8):1092-8. doi: 10.1177/1352458511433306. Epub 2012 Jun 13.
9
Two-year study of cervical cord volume and myelin water in primary progressive multiple sclerosis.原发性进行性多发性硬化症两年的颈髓体积和髓鞘水研究。
Mult Scler. 2010 Jun;16(6):670-7. doi: 10.1177/1352458510365586.
10
Brain atrophy evolution and lesion load accrual in multiple sclerosis: a 2-year follow-up study.多发性硬化症中脑萎缩的演变及病灶负荷累积:一项为期2年的随访研究。
Mult Scler. 2009 Feb;15(2):204-11. doi: 10.1177/1352458508098270. Epub 2008 Nov 5.

引用本文的文献

1
Brain Atrophy and Cognitive Impairment in Primary and Secondary Progressive Multiple Sclerosis Cohort-Similar Progressive MS Phenotype.原发进展型和继发进展型多发性硬化队列中的脑萎缩与认知障碍——相似的进展型多发性硬化表型
Int J Mol Sci. 2025 Sep 2;26(17):8523. doi: 10.3390/ijms26178523.
2
Towards a Unified Set of Diagnostic Criteria for Multiple Sclerosis.迈向多发性硬化症统一诊断标准集
Ann Neurol. 2025 Mar;97(3):571-582. doi: 10.1002/ana.27145. Epub 2024 Nov 28.
3
Contrast-Enhancing Lesion Segmentation in Multiple Sclerosis: A Deep Learning Approach Validated in a Multicentric Cohort.
多发性硬化症中对比增强病变分割:一种在多中心队列中验证的深度学习方法。
Bioengineering (Basel). 2024 Aug 22;11(8):858. doi: 10.3390/bioengineering11080858.
4
The prevalence and topography of spinal cord demyelination in multiple sclerosis: a retrospective study.多发性硬化症中脊髓脱髓鞘的患病率和分布:一项回顾性研究。
Acta Neuropathol. 2024 Mar 9;147(1):51. doi: 10.1007/s00401-024-02700-6.
5
Disease activity in primary progressive multiple sclerosis: a systematic review and meta-analysis.原发性进行性多发性硬化症的疾病活动:一项系统评价和荟萃分析。
Front Neurol. 2023 Nov 6;14:1277477. doi: 10.3389/fneur.2023.1277477. eCollection 2023.
6
Comparison of recent updates in genetics, immunology, biomarkers, and neuroimaging of primary-progressive and relapsing-remitting multiple sclerosis and the role of ocrelizumab in the management of their refractory cases.原发性进行性和复发缓解型多发性硬化症在遗传学、免疫学、生物标志物及神经影像学方面的最新进展比较以及奥瑞珠单抗在其难治性病例管理中的作用
Health Sci Rep. 2023 Jul 12;6(7):e1422. doi: 10.1002/hsr2.1422. eCollection 2023 Jul.
7
Granzyme B + CD8 + T cells with terminal differentiated effector signature determine multiple sclerosis progression.颗粒酶 B+CD8+具有终末分化效应器特征的 T 细胞决定多发性硬化症的进展。
J Neuroinflammation. 2023 Jun 2;20(1):138. doi: 10.1186/s12974-023-02810-0.
8
Magnetic Resonance Imaging in Primary Progressive Multiple Sclerosis Patients : Review.原发性进行性多发性硬化症患者的磁共振成像:综述。
Clin Neuroradiol. 2022 Sep;32(3):625-641. doi: 10.1007/s00062-022-01144-3. Epub 2022 Mar 8.
9
Association of Age With Contrast-Enhancing Lesions Across the Multiple Sclerosis Disease Spectrum.年龄与多发性硬化症疾病谱中强化病变的相关性。
Neurology. 2021 Sep 28;97(13):e1334-e1342. doi: 10.1212/WNL.0000000000012603. Epub 2021 Aug 10.
10
Diagnosis of Progressive Multiple Sclerosis From the Imaging Perspective: A Review.从影像学角度诊断进展性多发性硬化症:综述。
JAMA Neurol. 2021 Mar 1;78(3):351-364. doi: 10.1001/jamaneurol.2020.4689.