Wang Sumei, Melhem Elias R
Department of Radiology, Division of Neuroradiology, Hospital of the University of Pennsylvania, 3400 Spruce Street, Second Floor Dulles, Philadelphia, PA 19104, USA.
Ann N Y Acad Sci. 2005 Dec;1064:61-77. doi: 10.1196/annals.1340.013.
Amyotrophic lateral sclerosis (ALS), also called Lou Gehrig's disease, is a motor neuron disease characterized by progressive degeneration of upper motor neuron (UMN) and lower motor neuron (LMN), while primary lateral sclerosis (PLS) is defined by pure UMN involvement. A reliable objective marker of UMN involvement is critical for the early diagnosis and monitoring of disease progression in patients with ALS and PLS. Diffusion tensor imaging (DTI), magnetization transfer imaging (MTI), and magnetic resonance spectroscopy (MRS), which provide insight into the pathophysiological process of ALS and PLS, show great promise in this regard. Further investigation is needed to determine and to compare the utility of various neuroimaging markers.
肌萎缩侧索硬化症(ALS),也称为卢伽雷氏病,是一种运动神经元疾病,其特征是上运动神经元(UMN)和下运动神经元(LMN)进行性退化,而原发性侧索硬化症(PLS)则由单纯的UMN受累所定义。UMN受累的可靠客观标志物对于ALS和PLS患者的早期诊断和疾病进展监测至关重要。扩散张量成像(DTI)、磁化传递成像(MTI)和磁共振波谱(MRS)能够深入了解ALS和PLS的病理生理过程,在这方面显示出巨大的前景。需要进一步研究以确定并比较各种神经影像学标志物的效用。