Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Mov Disord. 2014 Mar;29(3):375-9. doi: 10.1002/mds.25688. Epub 2013 Sep 30.
Multiple system atrophy, a sporadic neurodegenerative disease, is characterized by the presence of high numbers of glial cytoplasmic inclusions mainly formed by α-synuclein protein, which is encoded by the SNCA gene. To date, however, few studies have investigated the plasma α-synuclein levels in patients with multiple system atrophy. We studied plasma α-synuclein concentrations by using an enzyme-linked immunosorbent assay in 74 patients with multiple system atrophy and 90 healthy controls. The plasma α-synuclein levels were significantly elevated in patients who had multiple system atrophy compared with the control group (P = 0.000). In a subgroup of 48 patients who had probable multiple system atrophy, there was a weakly negative correlation between plasma α-synuclein levels and subscores on Unified Multiple System Atrophy Rating Scale item VI (r(s) = -0.307; P = 0.034). Plasma α-synuclein levels were elevated in patients with multiple system atrophy, and these levels may be decreased with the development of disease.
多系统萎缩是一种散发性神经退行性疾病,其特征是存在大量由α-突触核蛋白组成的神经胶质细胞质包涵体,该蛋白由 SNCA 基因编码。然而,迄今为止,很少有研究调查多系统萎缩患者的血浆α-突触核蛋白水平。我们使用酶联免疫吸附试验研究了 74 例多系统萎缩患者和 90 例健康对照者的血浆α-突触核蛋白浓度。与对照组相比,多系统萎缩患者的血浆α-突触核蛋白水平显著升高(P=0.000)。在 48 例可能患有多系统萎缩的患者亚组中,血浆α-突触核蛋白水平与统一多系统萎缩评定量表项目 VI 的亚评分之间存在弱负相关(r(s)=-0.307;P=0.034)。多系统萎缩患者的血浆α-突触核蛋白水平升高,并且这些水平可能随着疾病的发展而降低。