Agosta Federica, Ferraro Pilar M, Riva Nilo, Spinelli Edoardo G, Chiò Adriano, Canu Elisa, Valsasina Paola, Lunetta Christian, Iannaccone Sandro, Copetti Massimiliano, Prudente Evelina, Comi Giancarlo, Falini Andrea, Filippi Massimo
Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Department of Neurology, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Hum Brain Mapp. 2016 Apr;37(4):1614-26. doi: 10.1002/hbm.23124. Epub 2016 Feb 2.
To assess the structural correlates of cognitive and behavioral impairment in motor neuron diseases (MND) using multimodal MRI.
One hundred one patients with sporadic MND (56 classic amyotrophic lateral sclerosis, 31 upper motor neuron phenotype, and 14 lower motor neuron phenotype) and 51 controls were enrolled. Patients were classified into MND with a pure motor syndrome (MND-motor) and with cognitive/behavioral symptoms (MND-plus). Cortical thickness measures and diffusion tensor (DT) metrics of white matter (WM) tracts were assessed. A random forest approach was used to explore the independent role of cortical and WM abnormalities in explaining major cognitive and behavioral symptoms.
There were 48 MND-motor and 53 MND-plus patients. Relative to controls, both patient groups showed a distributed cortical thinning of the bilateral precentral gyrus, insular and cingulate cortices, and frontotemporal regions. In all regions, there was a trend toward a more severe involvement in MND-plus cases, particularly in the temporal lobes. Both patient groups showed damage to the motor callosal fibers, which was more severe in MND-plus. MND-plus patients also showed a more severe involvement of the extra-motor WM tracts. The best predictors of executive and non-executive deficits and behavioral symptoms in MND were diffusivity abnormalities of the corpus callosum and frontotemporal tracts, including the uncinate, cingulum, and superior longitudinal fasciculi.
Cortical thinning and WM degeneration are highly associated with neuropsychological and behavioral symptoms in patients with MND. DT MRI metrics seem to be the most sensitive markers of extra-motor deficits within the MND spectrum.
使用多模态磁共振成像(MRI)评估运动神经元疾病(MND)中认知和行为障碍的结构相关性。
纳入101例散发性MND患者(56例经典肌萎缩侧索硬化症、31例上运动神经元表型和14例下运动神经元表型)和51例对照。患者被分为纯运动综合征的MND(MND-运动型)和伴有认知/行为症状的MND(MND-加型)。评估皮质厚度测量值和白质(WM)束的扩散张量(DT)指标。采用随机森林方法探讨皮质和WM异常在解释主要认知和行为症状中的独立作用。
有48例MND-运动型患者和53例MND-加型患者。相对于对照组,两组患者均表现出双侧中央前回、岛叶和扣带回皮质以及额颞区域的弥漫性皮质变薄。在所有区域,MND-加型病例的受累程度有更严重的趋势,尤其是在颞叶。两组患者均显示胼胝体运动纤维受损,在MND-加型中更严重。MND-加型患者还表现出运动外WM束的更严重受累。MND中执行和非执行功能缺陷及行为症状的最佳预测指标是胼胝体和额颞束的扩散异常,包括钩束、扣带束和上纵束。
皮质变薄和WM变性与MND患者的神经心理和行为症状高度相关。DT MRI指标似乎是MND谱系中运动外缺陷最敏感的标志物。