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Improved Stability of Whole Brain Surface Parcellation with Multi-Atlas Segmentation.通过多图谱分割提高全脑表面分区的稳定性
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Fingolimod effect on gray matter, thalamus, and white matter in patients with multiple sclerosis.芬戈莫德对多发性硬化症患者脑灰质、丘脑和白质的影响。
Neurology. 2018 Apr 10;90(15):e1324-e1332. doi: 10.1212/WNL.0000000000005292. Epub 2018 Mar 14.
3
Deep gray matter volume loss drives disability worsening in multiple sclerosis.深部灰质体积损失导致多发性硬化症残疾恶化。
Ann Neurol. 2018 Feb;83(2):210-222. doi: 10.1002/ana.25145. Epub 2018 Feb 6.
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Thalamic atrophy in multiple sclerosis: A magnetic resonance imaging marker of neurodegeneration throughout disease.多发性硬化症中的丘脑萎缩:疾病过程中神经退行性变的磁共振成像标志物。
Ann Neurol. 2018 Feb;83(2):223-234. doi: 10.1002/ana.25150. Epub 2018 Feb 9.
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Volumetric Analysis from a Harmonized Multisite Brain MRI Study of a Single Subject with Multiple Sclerosis.来自对一名多发性硬化症单一受试者的多站点脑磁共振成像(MRI)协调研究的容积分析。
AJNR Am J Neuroradiol. 2017 Aug;38(8):1501-1509. doi: 10.3174/ajnr.A5254. Epub 2017 Jun 22.
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Evaluating accuracy of striatal, pallidal, and thalamic segmentation methods: Comparing automated approaches to manual delineation.评估纹状体、苍白球和丘脑分割方法的准确性:比较自动方法与手动勾画。
Neuroimage. 2018 Apr 15;170:182-198. doi: 10.1016/j.neuroimage.2017.02.069. Epub 2017 Mar 1.
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Brain MRI atrophy quantification in MS: From methods to clinical application.多发性硬化症中脑MRI萎缩量化:从方法到临床应用
Neurology. 2017 Jan 24;88(4):403-413. doi: 10.1212/WNL.0000000000003542. Epub 2016 Dec 16.
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Robust skull stripping using multiple MR image contrasts insensitive to pathology.使用对病变不敏感的多个磁共振图像对比度进行稳健的颅骨剥离。
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Comparative efficacy of disease-modifying therapies for patients with relapsing remitting multiple sclerosis: Systematic review and network meta-analysis.比较缓解复发型多发性硬化症患者疾病修饰疗法的疗效:系统评价和网络荟萃分析。
Mult Scler Relat Disord. 2016 Sep;9:23-30. doi: 10.1016/j.msard.2016.06.001. Epub 2016 Jun 8.
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Consistent cortical reconstruction and multi-atlas brain segmentation.一致的皮质重建和多图谱脑部分割。
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疾病修正疗法对多发性硬化症患者皮质下灰质萎缩的影响。

Effect of disease-modifying therapies on subcortical gray matter atrophy in multiple sclerosis.

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD, USA.

出版信息

Mult Scler. 2020 Mar;26(3):312-321. doi: 10.1177/1352458519826364. Epub 2019 Feb 11.

DOI:10.1177/1352458519826364
PMID:30741108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6689465/
Abstract

BACKGROUND

The effects of disease-modifying therapies (DMTs) on region-specific brain atrophy in multiple sclerosis (MS) are unclear.

OBJECTIVE

To determine the effects of higher versus lower efficacy DMTs on rates of brain substructure atrophy in MS.

METHODS

A non-randomized, observational cohort of people with MS followed with annual brain magnetic resonance imaging (MRI) was evaluated retrospectively. Whole brain, subcortical gray matter (GM), cortical GM, and cerebral white matter (WM) volume fractions were obtained. DMTs were categorized as higher (DMT-H: natalizumab and rituximab) or lower (DMT-L: interferon-beta and glatiramer acetate) efficacy. Follow-up epochs were analyzed if participants had been on a DMT for ⩾6 months prior to baseline and had at least one follow-up MRI while on DMTs in the same category.

RESULTS

A total of 86 DMT epochs (DMT-H:  = 32; DMT-L:  = 54) from 78 participants fulfilled the study inclusion criteria. Mean follow-up was 2.4 years. Annualized rates of thalamic (-0.15% vs -0.81%;  = 0.001) and putaminal (-0.27% vs -0.73%;  = 0.001) atrophy were slower during DMT-H compared to DMT-L epochs. These results remained significant in multivariate analyses including demographics, clinical characteristics, and T2 lesion volume.

CONCLUSION

DMT-H treatment may be associated with slower rates of subcortical GM atrophy, especially of the thalamus and putamen. Thalamic and putaminal volumes are promising imaging biomarkers in MS.

摘要

背景

疾病修正疗法(DMT)对多发性硬化症(MS)特定区域脑萎缩的影响尚不清楚。

目的

确定更高与更低疗效 DMT 对 MS 脑亚结构萎缩率的影响。

方法

回顾性评估了一项非随机、观察性 MS 患者队列,每年进行脑磁共振成像(MRI)检查。获得全脑、皮质下灰质(GM)、皮质 GM 和脑白质(WM)体积分数。将 DMT 分为更高(DMT-H:那他珠单抗和利妥昔单抗)或更低(DMT-L:干扰素-β和聚乙二醇干扰素)疗效。如果参与者在基线前至少有 6 个月接受 DMT 治疗且在同一类别 DMT 治疗期间至少有一次后续 MRI,则分析随访期。

结果

共有 78 名参与者的 86 个 DMT 时期(DMT-H:=32;DMT-L:=54)符合研究纳入标准。平均随访时间为 2.4 年。DMT-H 与 DMT-L 时期相比,丘脑(-0.15%对-0.81%;=0.001)和壳核(-0.27%对-0.73%;=0.001)萎缩的年发生率较慢。在包括人口统计学、临床特征和 T2 病变体积在内的多变量分析中,这些结果仍然具有统计学意义。

结论

DMT-H 治疗可能与皮质下 GM 萎缩率较慢有关,特别是丘脑和壳核。丘脑和壳核体积是 MS 有前途的成像生物标志物。