Graph theory network analysis reveals widespread white matter damage in brains of patients with classic ALS.

Venkateswaran Rajagopalan, Erik P Pioro
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Abstract

Objective: Amyotrophic lateral sclerosis (ALS) exhibits several different presentations and clinical phenotypes. Of these, classic ALS (ALS-Cl), which is the most common phenotype, presents with relatively equal amounts of upper motor neuron and lower motor neuron signs. Magnetic resonance imaging (MRI) provides a noninvasive way to assess central nervous system damage in these patients. To our knowledge no study is available where exploratory whole brain grey matter (GM) and white matter (WM) network analysis is performed considering only the ALS-Cl subgroup of ALS patients. Methods: GM voxel-based morphometry analysis and WM network analysis using graph theory was performed in the MRI dataset of 14 neurologic controls and 25 ALS-Cl patients. Results and Conclusions: No significant GM differences were observed between ALS-Cl and neurologic controls. WM network revealed significant (p < 0.05) reduction and increase in degree measure in several extramotor brain regions of ALS-Cl patients. Both global and local graph metrics revealed significant abnormal values in ALS-Cl patients when compared to neurologic controls. Significant WM changes in ALS-Cl patients with no significant GM changes suggest that neurodegeneration may onset as an "axonopathy" in this ALS subtype.

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图论网络分析揭示了典型渐冻人症患者大脑中广泛的白质损伤。
目的:肌萎缩侧索硬化症(ALS)有几种不同的表现和临床表型。其中,典型 ALS(ALS-Cl)是最常见的表型,表现为相对等量的上运动神经元和下运动神经元症状。磁共振成像(MRI)是评估这些患者中枢神经系统损伤的一种无创方法。据我们所知,目前还没有研究仅针对 ALS-Cl 亚组患者进行全脑灰质(GM)和白质(WM)网络分析。研究方法对 14 名神经系统对照组和 25 名 ALS-Cl 患者的 MRI 数据集进行了基于体素的 GM 形态计量分析和基于图论的 WM 网络分析。结果和结论:在 ALS-Cl 和神经系统对照组之间未观察到明显的 GM 差异。WM 网络显示出明显的(p
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ALSUntangled #76: Wahls protocol. Graph theory network analysis reveals widespread white matter damage in brains of patients with classic ALS. Alteration in ornithine metabolism due to mutation in ALDH18A1 masquerading as ALS in pregnancy. Multistep modeling applied to a Malaysian ALS registry. Assessing disease progression in ALS: prognostic subgroups and outliers.
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