Finding Markers in Amyotrophic Lateral Sclerosis Diagnosis

B. Hern, Ez
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Abstract

Amyotrophic Lateral Sclerosis (ALS) is an uncommon illness, it is caused by moto neuron degeneration, upper, lower and bulbar muscles are affected. Some research also report degeneration in no motor structures of the brain. We proposed to evaluate Electrophysiological and Image techniques like markers in ALS diagnosis and correlate these results. During January 2015 to January 2017, twenty patients with ALS diagnosis and twenty health subjects were evaluated. Sensory and by motor nerve conduction studies, Electromyography, Somato- Sensory Evoked Potentials were done to the patients. 3T MRI image were obtained from the patients and from the health subjects. Post processing MRI techniques like voxel based morphometric, diffusion techniques and corticospinal tract and corpus callosum tractography were applied at different levels of the brain structures. Nerve conduction study was positive in 90% of the patients, SSEP were positive in 60% and EMG abnormalities were observed in 100% of patients. Anatomic MRI was positive in 50% of the patients. Fractional Anisotropy was reduced in ALS group in comparison with health group, more significant at cortex, internal capsule and corpus callosum. Fibers number of cortico-spinal tract and corpus callosum were diminished in ALS group in relation to health group. Also grey and white matter were reduce in ALS group, in areas such as: cingulate gyrus, anterior portion of occipital lobe, left caudate and putamen nucleus, right claustrum nucleus, lower and medium temporal gyrus bilateral, left precentral and post-central gyrus, corpus callosum, corticospinal tract, bilateral internal capsule, bilateral optical radiation, bilateral lower longitudinal fascicle, bilateral hippocampal fimbriae, bilateral radiated corona and pontocerebellar fibers. Electrophysiological studies confirmed ALS diagnosis in 100% of cases. MRI methods show abnormalities in motor and not motor structures of brain in ALS patients. They could be markers in early ALS diagnostic.
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寻找肌萎缩侧索硬化诊断标志物
肌萎缩性侧索硬化症(ALS)是一种罕见的疾病,它是由运动神经元变性引起的,上、下、球肌均受到影响。一些研究也报告了大脑无运动结构的退化。我们建议评估电生理和图像技术如标记物在ALS诊断中的作用,并将这些结果联系起来。2015年1月至2017年1月,对20例ALS诊断患者和20例健康受试者进行评估。对患者进行感觉及运动神经传导、肌电图、躯体-感觉诱发电位等检查。分别对患者和健康人进行3T MRI成像。基于体素的形态测量、扩散技术、皮质脊髓束和胼胝体束成像等后处理MRI技术在脑结构的不同层次上应用。90%的患者神经传导阳性,60%的患者SSEP阳性,100%的患者肌电图异常。50%的患者解剖MRI呈阳性。与健康组相比,肌萎缩侧索硬化症组的各向异性分数降低,在皮质、内囊和胼胝体上更为显著。肌萎缩侧索硬化症组皮质脊髓束和胼胝体纤维数量较健康组减少。ALS组脑灰质和白质减少的区域包括:扣带回、枕叶前部、左侧尾状核和壳核、右侧闭状核、双侧颞下回和中回、左侧中央前回和中央后回、胼胝体、皮质脊髓束、双侧内囊、双侧光辐射、双侧下纵束、双侧海马纤维、双侧辐射冠和桥小脑纤维。电生理研究100%证实了ALS的诊断。MRI方法显示ALS患者的大脑运动和非运动结构异常。它们可能是早期ALS诊断的标志。
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