Chen Yujing, Sun Sujuan, Yun Yan, Sun Xiaohan, Xin Jiaxiang, Shao Kai, Lin Pengfei, Yu Dexin, Yan Chuanzhu, Liu Shuangwu
Department of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.
Department of Radiology, Cheeloo College of Medicine, Qilu Hospital, Shandong University, Jinan, China.
Eur J Neurol. 2025 Jan;32(1):e16577. doi: 10.1111/ene.16577.
To date, no previous studies have used multishell diffusion MRI to identify striatal microstructural damage in vivo in amyotrophic lateral sclerosis (ALS) patients. Thus, in the present study, we aimed to comprehensively explore connectivity-based selective striatal subregion microstructural damage in sporadic ALS patients and its associations with motor disability, cognitive deficits, and serum biomarkers.
In this retrospective study, 79 ALS patients and 53 healthy controls (HCs) who underwent clinical assessment, serum neurofilament light (NfL) measurement, genetic testing, and multishell diffusion MRI scanning were included. Using a probabilistic tractography approach, the striatum was segmented into six subregions based on their corticostriatal connectivity. Three neurite orientation dispersion and density imaging (NODDI) parameters, the neurite density index (NDI), orientation dispersion index (ODI), and isotropic volume fraction (ISO), of the connectivity-based striatal subregions were measured.
Compared with HCs, ALS patients had a significantly lower NDI in the bilateral motor and right frontal subregions, a significantly lower ODI in the right motor and frontal subregions, and a significantly higher ISO in the bilateral motor and frontal subregions of the striatum after familywise error (p < 0.05). Moreover, striatal subregion microstructural damage was significantly correlated with motor disabilities, cognitive deficits, and serum NfL levels in ALS patients (p = 0.020-0.002).
Our study provides clear evidence demonstrating that connectivity-based selective striatal subregion microstructural damage is a definite feature of sporadic ALS patients and suggesting that striatal damage may play an important role in motor disability and cognitive deficits in ALS patients.
迄今为止,尚无研究使用多壳层扩散磁共振成像(MRI)在体识别肌萎缩侧索硬化症(ALS)患者纹状体的微观结构损伤。因此,在本研究中,我们旨在全面探究散发性ALS患者基于连接性的选择性纹状体亚区微观结构损伤及其与运动功能障碍、认知缺陷和血清生物标志物的关系。
在这项回顾性研究中,纳入了79例ALS患者和53名健康对照(HC),他们均接受了临床评估、血清神经丝轻链(NfL)测量、基因检测和多壳层扩散MRI扫描。采用概率纤维束成像方法,根据皮质-纹状体连接性将纹状体分为六个亚区。测量基于连接性的纹状体亚区的三个神经突方向离散度和密度成像(NODDI)参数,即神经突密度指数(NDI)、方向离散度指数(ODI)和各向同性体积分数(ISO)。
与HC相比;经家族性错误率校正后,ALS患者双侧运动和右侧额叶亚区的NDI显著降低,右侧运动和额叶亚区的ODI显著降低,双侧运动和额叶亚区纹状体的ISO显著升高(p < 0.05)。此外,ALS患者纹状体亚区微观结构损伤与运动功能障碍、认知缺陷和血清NfL水平显著相关(p = 0.020 - 0.002)。
我们的研究提供了明确的证据,证明基于连接性的选择性纹状体亚区微观结构损伤是散发性ALS患者的一个明确特征,并表明纹状体损伤可能在ALS患者的运动功能障碍和认知缺陷中起重要作用。