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多发性硬化症与健康状态下结构连接的对称性差异。

Symmetry differences of structural connectivity in multiple sclerosis and healthy state.

机构信息

Biomedical Engineering Department, Amirkabir University of Technology, Tehran, Iran.

Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Brain Res Bull. 2023 Dec;205:110816. doi: 10.1016/j.brainresbull.2023.110816. Epub 2023 Nov 14.

DOI:10.1016/j.brainresbull.2023.110816
PMID:37972899
Abstract

Focal and diffuse cerebral damages occur in Multiple Sclerosis (MS) that promotes profound shifts in local and global structural connectivity parameters, mainly derived from diffusion tensor imaging. Most of the reconstruction analyses have applied conventional tracking algorithms largely based on the controversial streamline count. For a more credible explanation of the diffusion MRI signal, we used convex optimization modeling for the microstructure-informed tractography2 (COMMIT2) framework. All multi-shell diffusion data from 40 healthy controls (HCs) and 40 relapsing-remitting MS (RRMS) patients were transformed into COMMIT2-weighted matrices based on the Schefer-200 parcels atlas (7 networks) and 14 bilateral subcortical regions. The success of the classification process between MS and healthy state was efficiently predicted by the left DMN-related structures and visual network-associated pathways. Additionally, the lesion volume and age of onset were remarkably correlated with the components of the left DMN. Using complementary approaches such as global metrics revealed differences in WM microstructural integrity between MS and HCs (efficiency, strength). Our findings demonstrated that the cutting-edge diffusion MRI biomarkers could hold the potential for interpreting brain abnormalities in a more distinctive way.

摘要

多发性硬化症(MS)会导致大脑局部和整体结构连接参数发生深刻变化,这主要源于弥散张量成像。大多数重构分析都应用了传统的跟踪算法,这些算法主要基于有争议的流线计数。为了更可信地解释弥散 MRI 信号,我们使用凸优化建模进行基于微观结构的轨迹追踪 2(COMMIT2)框架。基于 Schefer-200 区室图谱(7 个网络)和 14 个双侧皮质下区域,将来自 40 名健康对照(HC)和 40 名复发缓解型多发性硬化症(RRMS)患者的所有多壳弥散数据转换为 COMMIT2 加权矩阵。分类过程成功地预测了 MS 和健康状态之间的差异,这主要与左默认模式网络相关结构和视觉网络相关通路有关。此外,病变体积和发病年龄与左默认模式网络的组成部分显著相关。使用全局指标等补充方法揭示了 MS 和 HCs 之间 WM 微观结构完整性的差异(效率、强度)。我们的研究结果表明,前沿的弥散 MRI 生物标志物有可能以更独特的方式解释大脑异常。

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