From the Neuroimaging Research Unit (E.G.S., F.A., P.M.F., M.F.), Department of Neurology, Institute of Experimental Neurology, Division of Neuroscience (E.G.S., N.R., Y.F., G.C., M.F.), and Department of Neuroradiology and CERMAC (A.F.), San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Via Olgettina 60, 20132 Milan, Italy; and NEuroMuscular Omnicenter, Serena Onlus Foundation, Milan, Italy (C.L.).
Radiology. 2016 Aug;280(2):545-56. doi: 10.1148/radiol.2016151846. Epub 2016 Mar 9.
Purpose To investigate the patterns of cortical thinning and white matter tract damage in patients with lower motor neuron (LMN)-predominant disease compared with healthy control subjects and those with classic amyotrophic lateral sclerosis (ALS) and to evaluate the relationship between brain structural changes and clinical and cognitive features in these patients. Materials and Methods This study was approved by the local ethical committee, and written informed consent was obtained from all subjects before enrollment. Twenty-eight patients with LMN-predominant disease were compared with 55 patients with ALS and 56 healthy control subjects. Patients underwent a clinical and neuropsychological assessment and T1-weighted and diffusion-tensor magnetic resonance (MR) imaging. Surface-based morphometry was used to assess cortical thickness. Tract-based spatial statistics and tractography were used to study white matter tract damage. Results Patients with LMN-predominant disease did not show differences compared with healthy control subjects in cortical thickness and diffusion-tensor MR imaging metrics. Patients with ALS showed cortical thinning of the motor-related cortices and a distributed involvement of the prefrontal, temporal, and parietal gyri (P < .05, false discovery rate corrected). Patients with ALS also showed white matter damage along motor and extramotor tracts compared with control subjects and patients with LMN-predominant disease (tract-based spatial statistics: P < .05, family-wise error corrected; tractography: P values < .001 to .05, false discovery rate corrected). In patients with LMN-predominant disease, cognitive deficits correlated with alterations in diffusivity in the left cingulum (r = -0.66, P = .01) and superior longitudinal fasciculus (r = -0.65, P = .05). Conclusion Motor and extramotor cortical thinning and diffusion-tensor MR imaging alterations were specific for motor neuron disease phenotypes, with clinically overt upper motor neuron involvement. However, the lack of significant differences in cortical thickness between subjects with LMN-predominant disease and those with ALS and cognitive deficits associated with alterations in diffusivity in patients with LMN-predominant disease suggest that investigating brain structural and microstructural MR imaging features may provide markers of central nervous system damage in patients with rare motor neuron disease. (©) RSNA, 2016 Online supplemental material is available for this article.
目的 研究与健康对照组及经典肌萎缩侧索硬化症(ALS)患者相比,下运动神经元(LMN)为主型疾病患者的皮质变薄和白质束损伤模式,并评估这些患者脑结构变化与临床和认知特征之间的关系。 材料与方法 本研究经当地伦理委员会批准,所有入组患者均签署书面知情同意书。将 28 例 LMN 为主型疾病患者与 55 例 ALS 患者和 56 例健康对照组进行比较。所有患者均接受临床和神经心理学评估及 T1 加权和弥散张量磁共振(MR)成像检查。采用基于表面的形态计量学评估皮质厚度,基于束的空间统计和束追踪技术评估白质束损伤。 结果 LMN 为主型疾病患者的皮质厚度和弥散张量 MR 成像指标与健康对照组相比差异无统计学意义。ALS 患者表现为与运动相关皮质的皮质变薄和额、颞、顶叶脑回的分布性受累(P <.05,经假发现率校正)。与对照组和 LMN 为主型疾病患者相比,ALS 患者还表现出沿运动和运动外束的白质损伤(基于束的空间统计:P <.05,经全脑错误校正;束追踪:P 值<.001 至<.05,经假发现率校正)。在 LMN 为主型疾病患者中,认知缺陷与左侧扣带回(r = -0.66,P =.01)和上纵束(r = -0.65,P =.05)弥散率改变相关。 结论 运动和运动外皮质变薄及弥散张量 MR 成像改变与运动神经元病表型有关,且伴有明显的上运动神经元受累。然而,与 ALS 患者相比,LMN 为主型疾病患者皮质厚度无显著差异,且 LMN 为主型疾病患者的认知缺陷与弥散率改变有关,提示对脑结构和微观结构磁共振成像特征进行研究可能为罕见运动神经元病患者中枢神经系统损伤提供标志物。 (©)RSNA,2016 在线补充材料可在本文中获得。