• 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

高分辨率 T1 弛豫时间图显示了长期多发性硬化症中细微但具有临床意义的灰质损伤。

High-resolution T1-relaxation time mapping displays subtle, clinically relevant, gray matter damage in long-standing multiple sclerosis.

机构信息

Department of Radiology and Nuclear Medicine, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands/Department of Physics and Medical Technology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands

Department of Radiology and Nuclear Medicine, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands/Department of Physics and Medical Technology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Mult Scler. 2016 Sep;22(10):1279-88. doi: 10.1177/1352458515615953. Epub 2015 Nov 12.

DOI:10.1177/1352458515615953
PMID:26564997
Abstract

BACKGROUND

Gray matter (GM) pathology has high clinical relevance in multiple sclerosis (MS), but conventional magnetic resonance imaging (MRI) is insufficiently sensitive to visualize the rather subtle damage.

OBJECTIVE

To investigate whether high spatial resolution T1-relaxation time (T1-RT) measurements can detect changes in the normal-appearing GM of patients with long-standing MS and whether these changes are associated with physical and cognitive impairment.

METHODS

High spatial resolution (1.05 × 1.05 × 1.2 mm(3)) T1-RT measurements were performed at 3 T in 156 long-standing MS patients and 54 healthy controls. T1-RT histogram parameters in several regions were analyzed to investigate group differences. Stepwise linear regression analyses were used to assess the relation of T1-RT with physical and cognitive impairment.

RESULTS

In both thalamus and cortex, T1-RT histogram skewness was higher in patients than controls. In the cortex, this was driven by the frontal and temporal lobes. No differences were found in other GM histogram parameters. Cortical skewness, thalamus volume, and average white matter (WM) lesion T1-RT emerged as the strongest predictors for cognitive performance (adjusted R(2) = 0.39).

CONCLUSION

Subtle GM damage was present in the cortex and thalamus of MS patients, as indicated by increased T1-RT skewness. Increased cortical skewness emerged as an independent predictor of cognitive dysfunction.

摘要

背景

灰质(GM)病理学在多发性硬化症(MS)中有很高的临床相关性,但常规磁共振成像(MRI)的敏感性不足以观察到相当微妙的损伤。

目的

研究高空间分辨率 T1 弛豫时间(T1-RT)测量是否可以检测到长期 MS 患者正常外观 GM 的变化,以及这些变化是否与身体和认知障碍有关。

方法

在 3T 下对 156 名长期 MS 患者和 54 名健康对照者进行高空间分辨率(1.05×1.05×1.2mm³)T1-RT 测量。分析了几个区域的 T1-RT 直方图参数以研究组间差异。采用逐步线性回归分析评估 T1-RT 与身体和认知障碍的关系。

结果

在丘脑和皮质中,患者的 T1-RT 直方图偏度均高于对照组。在皮质中,这是由额叶和颞叶驱动的。在其他 GM 直方图参数中未发现差异。皮质偏度、丘脑体积和平均白质(WM)病变 T1-RT 是认知表现的最强预测因子(调整后的 R²=0.39)。

结论

MS 患者的皮质和丘脑存在细微的 GM 损伤,表现为 T1-RT 偏度增加。增加的皮质偏度是认知功能障碍的独立预测因子。

相似文献

1
High-resolution T1-relaxation time mapping displays subtle, clinically relevant, gray matter damage in long-standing multiple sclerosis.高分辨率 T1 弛豫时间图显示了长期多发性硬化症中细微但具有临床意义的灰质损伤。
Mult Scler. 2016 Sep;22(10):1279-88. doi: 10.1177/1352458515615953. Epub 2015 Nov 12.
2
Gray matter trophism, cognitive impairment, and depression in patients with multiple sclerosis.多发性硬化症患者的灰质营养、认知障碍和抑郁。
Mult Scler. 2017 Dec;23(14):1864-1874. doi: 10.1177/1352458517692886. Epub 2017 Feb 7.
3
Single scan quantitative gradient recalled echo MRI for evaluation of tissue damage in lesions and normal appearing gray and white matter in multiple sclerosis.单次扫描定量梯度回波 MRI 评估多发性硬化症病变及正常表现的灰白质组织损伤。
J Magn Reson Imaging. 2019 Feb;49(2):487-498. doi: 10.1002/jmri.26218. Epub 2018 Aug 29.
4
Detection and quantification of regional cortical gray matter damage in multiple sclerosis utilizing gradient echo MRI.利用梯度回波磁共振成像检测和量化多发性硬化症中局部皮质灰质损伤
Neuroimage Clin. 2015 Aug 18;9:164-75. doi: 10.1016/j.nicl.2015.08.003. eCollection 2015.
5
Changes of brain parenchyma free water fraction reflect tissue damage and impaired processing speed in multiple sclerosis.脑实质自由水分数的变化反映了多发性硬化中的组织损伤和处理速度受损。
Hum Brain Mapp. 2024 Jun 15;45(9):e26761. doi: 10.1002/hbm.26761.
6
Progression of regional atrophy in the left hemisphere contributes to clinical and cognitive deterioration in multiple sclerosis: A 5-year study.左侧半球区域性萎缩的进展导致多发性硬化症的临床和认知恶化:一项 5 年研究。
Hum Brain Mapp. 2017 Nov;38(11):5648-5665. doi: 10.1002/hbm.23755. Epub 2017 Aug 9.
7
Multi-parametric structural magnetic resonance imaging in relation to cognitive dysfunction in long-standing multiple sclerosis.多参数结构磁共振成像与长期多发性硬化认知功能障碍的关系。
Mult Scler. 2016 Apr;22(5):608-19. doi: 10.1177/1352458515596598. Epub 2015 Jul 24.
8
Cortical atrophy patterns in multiple sclerosis are non-random and clinically relevant.多发性硬化症中的皮质萎缩模式具有非随机性且与临床相关。
Brain. 2016 Jan;139(Pt 1):115-26. doi: 10.1093/brain/awv337. Epub 2015 Dec 4.
9
The association of cognitive impairment with gray matter atrophy and cortical lesion load in clinically isolated syndrome.认知障碍与临床孤立综合征的灰质萎缩和皮质病变负荷的关系。
Mult Scler Relat Disord. 2016 Nov;10:14-21. doi: 10.1016/j.msard.2016.08.008. Epub 2016 Aug 16.
10
NODDI, diffusion tensor microstructural abnormalities and atrophy of brain white matter and gray matter contribute to cognitive impairment in multiple sclerosis.神经突方向离散与密度成像(NODDI)、脑白质和灰质的扩散张量微观结构异常及萎缩导致多发性硬化症的认知障碍。
J Neurol. 2023 Feb;270(2):810-823. doi: 10.1007/s00415-022-11415-1. Epub 2022 Oct 6.

引用本文的文献

1
Validation of retroactively derived T1 relaxation values from 3D T1-weighted images with clinical and MRI measures of disability in multiple sclerosis.通过临床和MRI残疾测量指标对从三维T1加权图像追溯得出的T1弛豫值进行验证:多发性硬化症研究
PLoS One. 2025 May 19;20(5):e0323898. doi: 10.1371/journal.pone.0323898. eCollection 2025.
2
T1 mapping using MP2RAGE in degenerative cervical myelopathy: a longitudinal study.使用 MP2RAGE 进行 T1 映射在退行性颈椎脊髓病中的纵向研究。
Eur Spine J. 2025 Feb;34(2):731-740. doi: 10.1007/s00586-025-08652-z. Epub 2025 Jan 9.
3
Hippocampal subfields and thalamic nuclei associations with clinical outcomes in multiple sclerosis: An ultrahigh field MRI study.
海马亚区和丘脑核与多发性硬化临床结局的相关性:一项超高场 MRI 研究。
Mult Scler Relat Disord. 2024 Jun;86:105520. doi: 10.1016/j.msard.2024.105520. Epub 2024 Feb 27.
4
Lower myelin content is associated with more rapid cognitive decline among cognitively unimpaired individuals.髓鞘含量降低与认知正常个体认知能力下降更快有关。
Alzheimers Dement. 2023 Jul;19(7):3098-3107. doi: 10.1002/alz.12968. Epub 2023 Jan 31.
5
Assessment of cognitive impairment after acute cerebral infarction with T1 relaxation time measured by MP2RAGE sequence and cerebral hemodynamic by transcranial Doppler.采用MP2RAGE序列测量T1弛豫时间及经颅多普勒评估急性脑梗死患者的认知功能障碍及脑血流动力学
Front Neurol. 2022 Dec 6;13:1056423. doi: 10.3389/fneur.2022.1056423. eCollection 2022.
6
Clinical and Research MRI Techniques for Assessing Spinal Cord Integrity in Degenerative Cervical Myelopathy-A Scoping Review.评估退行性颈椎脊髓病中脊髓完整性的临床与研究性磁共振成像技术——一项范围综述
Biomedicines. 2022 Oct 18;10(10):2621. doi: 10.3390/biomedicines10102621.
7
First clinical application of a novel T1 mapping of the whole brain.首例新型全脑 T1 映射的临床应用。
Neuroradiol J. 2022 Dec;35(6):684-691. doi: 10.1177/19714009221084244. Epub 2022 Apr 21.
8
Relaxation-Compensated Chemical Exchange Saturation Transfer MRI in the Brain at 7T: Application in Relapsing-Remitting Multiple Sclerosis.7T下大脑的弛豫补偿化学交换饱和转移磁共振成像:在复发缓解型多发性硬化症中的应用
Front Neurol. 2022 Feb 25;13:764690. doi: 10.3389/fneur.2022.764690. eCollection 2022.
9
T1 Relaxation Times in the Cortex and Thalamus Are Associated With Working Memory and Information Processing Speed in Patients With Multiple Sclerosis.多发性硬化症患者大脑皮质和丘脑的T1弛豫时间与工作记忆及信息处理速度相关。
Front Neurol. 2021 Dec 3;12:789812. doi: 10.3389/fneur.2021.789812. eCollection 2021.
10
Whole brain 3D MR fingerprinting in multiple sclerosis: a pilot study.多发性硬化症的全脑 3D MR 指纹成像:一项初步研究。
BMC Med Imaging. 2021 May 22;21(1):88. doi: 10.1186/s12880-021-00620-5.