平化:多发性硬化症患者脊髓沿水平弥散张量成像。

Frontiers in neuroimaging Pub Date : 2025-08-11 eCollection Date: 2025-01-01 DOI:10.3389/fnimg.2025.1599966
Atlee A Witt, Anna J E Combes, Grace Sweeney, Logan E Prock, Delaney Houston, Seth Stubblefield, Colin D McKnight, Kristin P O'Grady, Seth A Smith, Kurt G Schilling
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引用次数: 0

摘要

简介:多发性硬化症(MS)是一种以脱髓鞘和轴突变性为特征的慢性神经炎症性疾病,这一过程可以通过弥散张量成像(DTI)来探测。在大脑中,白质(WM)束状图能够对微结构变化进行解剖特异性分析。然而,在脊髓(SC)中,解剖定位本质上是由颈椎水平定义的,为区域分析提供了另一种框架。方法:本研究采用一种横向方法来评估复发-缓解型多发性硬化症(pwRRMS)患者相对于健康对照(hc)的SC的微观结构(如分数各向异性)和宏观结构(如横截面积)特征。结果:与传统的全脊髓平均相比,沿水平分析提高了对组差异的敏感性。WM束和灰质(GM)亚区的详细分割显示沿脊髓和轴向横截面的空间离散变化。值得注意的是,虽然GM萎缩与临床残疾有关,但微结构变化与残疾措施没有显着相关性。讨论:这些发现强调了水平特异性分析在检测局部病理中的效用,并提出了一种表征MS中SC改变的完善框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leveling up: along-level diffusion tensor imaging in the spinal cord of multiple sclerosis patients.

Introduction: Multiple sclerosis (MS) is a chronic neuroinflammatory disease marked by demyelination and axonal degeneration, processes that can be probed using diffusion tensor imaging (DTI). In the brain, white matter (WM) tractography enables anatomically specific analysis of microstructural changes. However, in the spinal cord (SC), anatomical localization is inherently defined by cervical levels, offering an alternative framework for regional analysis.

Methods: This study employed an along-level approach to assess both microstructural (e.g., fractional anisotropy) and macrostructural (e.g., cross-sectional area) features of the SC in persons with relapsing-remitting MS (pwRRMS) relative to healthy controls (HCs).

Results: Compared to conventional whole-cord averaging, along-level analyses provided enhanced sensitivity to group differences. Detailed segmentation of WM tracts and gray matter (GM) subregions revealed spatially discrete alterations along the cord and within axial cross-sections. Notably, while GM atrophy was associated with clinical disability, microstructural changes did not exhibit significant correlations with disability measures.

Discussion: These findings underscore the utility of level-specific analysis in detecting localized pathology and suggest a refined framework for characterizing SC alterations in MS.

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