• 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

复发缓解型和继发进展型多发性硬化症中病变及病变外皮质灰质的特征:一项磁化传递和扩散张量成像研究。

Characteristics of lesional and extra-lesional cortical grey matter in relapsing-remitting and secondary progressive multiple sclerosis: A magnetisation transfer and diffusion tensor imaging study.

作者信息

Yaldizli Özgür, Pardini Matteo, Sethi Varun, Muhlert Nils, Liu Zheng, Tozer Daniel J, Samson Rebecca S, Wheeler-Kingshott Claudia Am, Yousry Tarek A, Miller David H, Chard Declan T

机构信息

Queen Square MS Centre, UCL Institute of Neurology, UK/MS Center, University Hospital Basel, Switzerland

Queen Square MS Centre, UCL Institute of Neurology, UK/Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Italy.

出版信息

Mult Scler. 2016 Feb;22(2):150-9. doi: 10.1177/1352458515586085. Epub 2015 May 26.

DOI:10.1177/1352458515586085
PMID:26014608
Abstract

BACKGROUND

In multiple sclerosis (MS), diffusion tensor and magnetisation transfer imaging are both abnormal in lesional and extra-lesional cortical grey matter, but differences between clinical subtypes and associations with clinical outcomes have only been partly assessed.

OBJECTIVE

To compare mean diffusivity, fractional anisotropy and magnetisation transfer ratio (MTR) in cortical grey matter lesions (detected using phase-sensitive inversion recovery (PSIR) imaging) and extra-lesional cortical grey matter, and assess associations with disability in relapse-onset MS.

METHODS

Seventy-two people with MS (46 relapsing-remitting (RR), 26 secondary progressive (SP)) and 36 healthy controls were included in this study. MTR, mean diffusivity and fractional anisotropy were measured in lesional and extra-lesional cortical grey matter.

RESULTS

Mean fractional anisotropy was higher and MTR lower in lesional compared with extra-lesional cortical grey matter. In extra-lesional cortical grey matter mean fractional anisotropy and MTR were lower, and mean diffusivity was higher in the MS group compared with controls. Mean MTR was lower and mean diffusivity was higher in lesional and extra-lesional cortical grey matter in SPMS when compared with RRMS. These differences were independent of disease duration. In multivariate analyses, MTR in extra-lesional more so than lesional cortical grey matter was associated with disability.

CONCLUSION

Magnetic resonance abnormalities in lesional and extra-lesional cortical grey matter are greater in SPMS than RRMS. Changes in extra-lesional compared with lesional cortical grey matter are more consistently associated with disability.

摘要

背景

在多发性硬化症(MS)中,扩散张量成像和磁化传递成像在病灶及病灶外皮质灰质中均显示异常,但临床亚型之间的差异以及与临床结局的关联仅得到部分评估。

目的

比较皮质灰质病灶(使用相位敏感反转恢复(PSIR)成像检测)和病灶外皮质灰质中的平均扩散率、分数各向异性和磁化传递率(MTR),并评估复发型MS中与残疾的关联。

方法

本研究纳入了72例MS患者(46例复发缓解型(RR),26例继发进展型(SP))和36名健康对照者。测量病灶及病灶外皮质灰质中的MTR、平均扩散率和分数各向异性。

结果

与病灶外皮质灰质相比,病灶内的平均分数各向异性更高,MTR更低。在病灶外皮质灰质中,MS组的平均分数各向异性和MTR更低,平均扩散率更高。与RRMS相比,SPMS病灶及病灶外皮质灰质中的平均MTR更低,平均扩散率更高。这些差异与病程无关。在多变量分析中,病灶外而非病灶内皮质灰质的MTR与残疾相关。

结论

SPMS病灶及病灶外皮质灰质中的磁共振异常比RRMS更明显。与病灶内皮质灰质相比,病灶外皮质灰质的变化与残疾的相关性更一致。

相似文献

1
Characteristics of lesional and extra-lesional cortical grey matter in relapsing-remitting and secondary progressive multiple sclerosis: A magnetisation transfer and diffusion tensor imaging study.复发缓解型和继发进展型多发性硬化症中病变及病变外皮质灰质的特征:一项磁化传递和扩散张量成像研究。
Mult Scler. 2016 Feb;22(2):150-9. doi: 10.1177/1352458515586085. Epub 2015 May 26.
2
Investigation of outer cortical magnetisation transfer ratio abnormalities in multiple sclerosis clinical subgroups.多发性硬化症临床亚组中外皮质磁化传递率异常的研究。
Mult Scler. 2014 Sep;20(10):1322-30. doi: 10.1177/1352458514522537. Epub 2014 Feb 19.
3
Spinal cord grey matter abnormalities are associated with secondary progression and physical disability in multiple sclerosis.脊髓灰质异常与多发性硬化症的继发性进展和身体残疾有关。
J Neurol Neurosurg Psychiatry. 2015 Jun;86(6):608-14. doi: 10.1136/jnnp-2014-308241. Epub 2014 Aug 5.
4
Cervical cord area is associated with infratentorial grey and white matter volume predominantly in relapsing-remitting multiple sclerosis: A study using semi-automated cord volumetry and voxel-based morphometry.在复发缓解型多发性硬化症中,颈髓区域主要与幕下灰质和白质体积相关:一项使用半自动脊髓容积测量法和基于体素的形态测量学的研究
Mult Scler Relat Disord. 2015 May;4(3):264-72. doi: 10.1016/j.msard.2015.04.003. Epub 2015 Apr 15.
5
Magnetisation transfer ratio abnormalities in primary and secondary progressive multiple sclerosis.原发进展型和继发进展型多发性硬化症中的磁化传递率异常。
Mult Scler. 2020 May;26(6):679-687. doi: 10.1177/1352458519841810. Epub 2019 Apr 8.
6
Determinants of disability in multiple sclerosis at various disease stages: a multiparametric magnetic resonance study.多发性硬化症不同疾病阶段残疾的决定因素:一项多参数磁共振研究。
Arch Neurol. 2007 Aug;64(8):1163-8. doi: 10.1001/archneur.64.8.1163.
7
Sulcal and gyral crown cortical grey matter involvement in multiple sclerosis: A magnetisation transfer ratio study.脑沟和脑回顶部皮质灰质受累于多发性硬化症:一项磁化传递率研究。
Mult Scler Relat Disord. 2013 Jul;2(3):204-12. doi: 10.1016/j.msard.2013.01.001. Epub 2013 Feb 13.
8
Magnetization transfer ratio in lesions rather than normal-appearing brain relates to disability in patients with multiple sclerosis.病变磁化传递率与多发性硬化症患者的残疾相关,而不是与正常表现的大脑相关。
J Neurol. 2015 Aug;262(8):1909-17. doi: 10.1007/s00415-015-7793-5. Epub 2015 Jun 5.
9
Disability in progressive MS is associated with T2 lesion changes.进展性多发性硬化症中的残疾与 T2 病变变化有关。
Mult Scler Relat Disord. 2018 Feb;20:73-77. doi: 10.1016/j.msard.2017.12.010. Epub 2017 Dec 18.
10
Investigation of grey matter abnormalities in multiple sclerosis patients by combined use of double inversion recovery sequences and diffusion tensor MRI at 3.0 Tesla.3.0特斯拉下联合使用双反转恢复序列和扩散张量磁共振成像对多发性硬化症患者灰质异常的研究。
Clin Radiol. 2018 Sep;73(9):834.e17-834.e23. doi: 10.1016/j.crad.2018.04.016. Epub 2018 Jun 1.

引用本文的文献

1
Should We Consider Neurodegeneration by Itself or in a Triangulation with Neuroinflammation and Demyelination? The Example of Multiple Sclerosis and Beyond.我们应该单独考虑神经退行性变,还是将其与神经炎症和脱髓鞘联系起来综合考量?以多发性硬化症及其他疾病为例。
Int J Mol Sci. 2024 Nov 25;25(23):12637. doi: 10.3390/ijms252312637.
2
The cognitive relevance of non-lesional damage to cortical networks in people with multiple sclerosis.多发性硬化症患者皮质网络非病灶性损伤的认知相关性。
J Neurol. 2024 Jun;271(6):3203-3214. doi: 10.1007/s00415-024-12240-4. Epub 2024 Mar 5.
3
Understanding the Pathophysiology and Magnetic Resonance Imaging of Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorders.
了解多发性硬化症和视神经脊髓炎谱系疾病的病理生理学和磁共振成像。
Korean J Radiol. 2023 Dec;24(12):1260-1283. doi: 10.3348/kjr.2023.0360.
4
Quantitative magnetization transfer imaging in relapsing-remitting multiple sclerosis: a systematic review and meta-analysis.复发缓解型多发性硬化症的定量磁化传递成像:系统评价与荟萃分析。
Brain Commun. 2022 Apr 4;4(2):fcac088. doi: 10.1093/braincomms/fcac088. eCollection 2022.
5
The neuroradiology of progressive multifocal leukoencephalopathy: a clinical trial perspective.进行性多灶性白质脑病的神经放射学:临床试验视角。
Brain. 2022 Apr 18;145(2):426-440. doi: 10.1093/brain/awab419.
6
Regional grey matter microstructural changes and volume loss according to disease duration in multiple sclerosis patients.多发性硬化症患者根据疾病持续时间的区域性灰质微观结构变化和体积损失。
Sci Rep. 2021 Aug 19;11(1):16805. doi: 10.1038/s41598-021-96132-x.
7
Clinical significance of cortical lesions in patients with multiple sclerosis: A neuropsychological and neuroimaging study.多发性硬化症患者皮质病变的临床意义:一项神经心理学和神经影像学研究。
Brain Behav. 2018 Feb 14;8(3):e00934. doi: 10.1002/brb3.934. eCollection 2018 Mar.
8
In vivo characterization of cortical and white matter neuroaxonal pathology in early multiple sclerosis.早期多发性硬化症中皮质和白质神经轴突病变的体内特征分析
Brain. 2017 Nov 1;140(11):2912-2926. doi: 10.1093/brain/awx247.
9
Sensitivity of multi-shell NODDI to multiple sclerosis white matter changes: a pilot study.多壳层神经突方向离散与密度成像(NODDI)对多发性硬化症白质变化的敏感性:一项初步研究。
Funct Neurol. 2017 Apr/Jun;32(2):97-101. doi: 10.11138/fneur/2017.32.2.097.