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本文引用的文献

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The effects of antipsychotics on the brain: what have we learnt from structural imaging of schizophrenia?--a systematic review.抗精神病药物对大脑的影响:我们从精神分裂症的结构成像中学到了什么?——一项系统综述。
Curr Pharm Des. 2009;15(22):2535-49. doi: 10.2174/138161209788957456.
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Progression of gray matter atrophy and its association with white matter lesions in relapsing-remitting multiple sclerosis.复发缓解型多发性硬化症中灰质萎缩的进展及其与白质病变的关联。
J Neurol Sci. 2009 Oct 15;285(1-2):268-9; author reply 269. doi: 10.1016/j.jns.2009.05.020. Epub 2009 Jun 4.
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Different white matter lesion characteristics correlate with distinct grey matter abnormalities on magnetic resonance imaging in secondary progressive multiple sclerosis.
Mult Scler. 2009 Jun;15(6):687-94. doi: 10.1177/1352458509103176. Epub 2009 May 12.
4
Signal abnormalities on 1.5 and 3 Tesla brain MRI in multiple sclerosis patients and healthy controls. A morphological and spatial quantitative comparison study.多发性硬化症患者和健康对照者1.5和3特斯拉脑部磁共振成像的信号异常。一项形态学和空间定量比较研究。
Neuroimage. 2009 Oct 1;47(4):1352-62. doi: 10.1016/j.neuroimage.2009.04.019. Epub 2009 Apr 14.
5
Voxel-wise assessment of progression of regional brain atrophy in relapsing-remitting multiple sclerosis.复发缓解型多发性硬化症中区域脑萎缩进展的体素水平评估
J Neurol Sci. 2009 Jul 15;282(1-2):55-60. doi: 10.1016/j.jns.2009.02.322. Epub 2009 Mar 16.
6
Contribution of white matter lesions to gray matter atrophy in multiple sclerosis: evidence from voxel-based analysis of T1 lesions in the visual pathway.白质病变对多发性硬化症灰质萎缩的影响:基于体素的视觉通路T1病变分析证据
Arch Neurol. 2009 Feb;66(2):173-9. doi: 10.1001/archneurol.2008.562.
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Regional DTI differences in multiple sclerosis patients.多发性硬化症患者的区域弥散张量成像差异
Neuroimage. 2009 Feb 15;44(4):1397-403. doi: 10.1016/j.neuroimage.2008.10.026. Epub 2008 Nov 5.
8
Association of regional gray matter volume loss and progression of white matter lesions in multiple sclerosis - A longitudinal voxel-based morphometry study.多发性硬化症中区域灰质体积损失与白质病变进展的关联——一项基于体素的纵向形态学研究。
Neuroimage. 2009 Mar 1;45(1):60-7. doi: 10.1016/j.neuroimage.2008.10.006. Epub 2008 Oct 25.
9
Segmentation of brain magnetic resonance images for measurement of gray matter atrophy in multiple sclerosis patients.用于测量多发性硬化症患者灰质萎缩的脑磁共振图像分割
Neuroimage. 2009 Feb 1;44(3):769-76. doi: 10.1016/j.neuroimage.2008.09.059. Epub 2008 Oct 22.
10
Dirty-appearing white matter in multiple sclerosis: preliminary observations of myelin phospholipid and axonal loss.多发性硬化症中外观异常的白质:髓磷脂磷脂和轴突损失的初步观察
J Neurol. 2008 Nov;255(11):1802-11. doi: 10.1007/s00415-008-0002-z. Epub 2008 Sep 24.

复发缓解型多发性硬化症患者脑白质容积的时空分布模式及其与局部灰质容积减少的相关性。

Spatiotemporal distribution pattern of white matter lesion volumes and their association with regional grey matter volume reductions in relapsing-remitting multiple sclerosis.

机构信息

Medical Image Analysis Center, University Hospital Basel, CH-4031 Basel, Switzerland.

出版信息

Hum Brain Mapp. 2010 Oct;31(10):1542-55. doi: 10.1002/hbm.20951.

DOI:10.1002/hbm.20951
PMID:20108225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6870732/
Abstract

The association of white matter (WM) lesions and grey matter (GM) atrophy is a feature in relapsing-remitting multiple sclerosis (RRMS). The spatiotemporal distribution pattern of WM lesions, their relations to regional GM changes and the underlying dynamics are unclear. Here we combined parametric and non-parametric voxel-based morphometry (VBM) to clarify these issues. MRI data from RRMS patients with progressive (PLV, n = 45) and non-progressive WM lesion volumes (NPLV, n = 44) followed up for 12 months were analysed. Cross-sectionally, the spatial WM lesion distribution was compared using lesion probability maps (LPMs). Longitudinally, WM lesions and GM volumes were studied using FSL-VBM and SPM5-VBM, respectively. WM lesions clustered around the lateral ventricles and in the centrum semiovale with a more widespread pattern in the PLV than in the NPLV group. The maximum local probabilities were similar in both groups and higher for T2 lesions (PLV: 27%, NPLV: 25%) than for T1 lesions (PLV: 15%, NPLV 14%). Significant WM lesion changes accompanied by cortical GM volume reductions occurred in the corpus callosum and optic radiations (P = 0.01 corrected), and more liberally tested (uncorrected P < 0.01) in the inferior fronto-occipital and longitudinal fasciculi, and corona radiata in the PLV group. Not any WM or GM changes were found in the NPLV group. In the PLV group, WM lesion distribution and development in fibres, was associated with regional GM volume loss. The different spatiotemporal distribution patterns of patients with progressive compared to patients with non-progressive WM lesions suggest differences in the dynamics of pathogenesis.

摘要

脑白质(WM)病变和灰质(GM)萎缩的相关性是复发缓解型多发性硬化症(RRMS)的特征之一。WM 病变的时空分布模式、与区域性 GM 变化的关系及其潜在的动力学机制尚不清楚。本研究结合参数和非参数基于体素的形态计量学(VBM)来阐明这些问题。分析了随访 12 个月的进展性(PLV,n = 45)和非进展性 WM 病变体积(NPLV,n = 44)RRMS 患者的 MRI 数据。在横断面上,使用病变概率图(LPM)比较空间 WM 病变分布。在纵向,分别使用 FSL-VBM 和 SPM5-VBM 研究 WM 病变和 GM 体积。WM 病变集中在侧脑室周围和半卵圆中心,PLV 组的病变分布比 NPLV 组更广泛。两组的最大局部概率相似,T2 病变(PLV:27%,NPLV:25%)的概率高于 T1 病变(PLV:15%,NPLV:14%)。在胼胝体和视辐射中观察到显著的 WM 病变变化伴随着皮质 GM 体积减少(校正后 P = 0.01),在 PLV 组中更广泛地检测到(未校正 P < 0.01)在下额枕下束和纵束,以及放射冠。在 NPLV 组中未发现任何 WM 或 GM 变化。在 PLV 组中,WM 病变的分布和纤维的发展与局部 GM 体积减少相关。与非进展性 WM 病变患者相比,进展性 WM 病变患者具有不同的时空分布模式,提示发病机制的动力学差异。