Department of Neurology, Bongseng Memorial Hospital, Busan, Korea.
J Clin Neurol. 2011 Dec;7(4):215-22. doi: 10.3988/jcn.2011.7.4.215. Epub 2011 Dec 29.
The detection of α-synuclein in the body fluids of patients with synucleinopathy has yielded promising but inconclusive results, in part because of conformational changes of α-synuclein in response to environmental conditions. The aim of this study was to determine the feasibility of using α-synuclein as a biological marker for Parkinson's disease (PD).
Twenty-three drug-naïve patients with PD (age 62.4±12.7 years, mean±SD; 11 males) and 29 age- and sex-matched neurologic control subjects (age 60.1±16.2 years; 16 males) were recruited. The levels of oligomeric and total α-synuclein in the cerebrospinal fluid (CSF) and plasma were measured using two simultaneous enzyme-linked immunosorbent assays.
The level of α-synuclein oligomer in the CSF of PD patients was significantly higher in PD patients than in neurological controls, but other findings (plasma α-synuclein oligomer and total α-synuclein in CSF and plasma) did not differ significantly between the two groups. When the control subjects were divided into a symptomatic control group (11 patients who complained of parkinsonian symptoms and were diagnosed with hydrocephalus and drug-induced or vascular parkinsonism) and a neurologic control group (10 normal subjects and 8 patients with diabetic ophthalmoplegia), the level of α-synuclein oligomer in the CSF was still significantly higher in PD patients than in both of the control subgroups.
These findings provide further evidence for a pathogenic role of the α-synuclein oligomer and suggest that CSF levels of α-synuclein oligomer can be a reliable marker for PD.
在突触核蛋白病患者的体液中检测到α-突触核蛋白,结果有一定前景但尚无定论,部分原因是α-突触核蛋白在环境条件下发生构象改变。本研究旨在确定α-突触核蛋白是否可作为帕金森病(PD)的生物标志物。
纳入 23 例未经药物治疗的 PD 患者(年龄 62.4±12.7 岁,均值±标准差;11 例男性)和 29 例年龄和性别匹配的神经科对照组(年龄 60.1±16.2 岁;16 例男性)。使用两种同步酶联免疫吸附测定法检测脑脊液(CSF)和血浆中寡聚体和总α-突触核蛋白的水平。
PD 患者 CSF 中α-突触核蛋白寡聚体的水平明显高于神经科对照组,但其他发现(血浆α-突触核蛋白寡聚体和 CSF 及血浆中的总α-突触核蛋白)在两组之间无显著差异。当对照组分为有症状对照组(11 例主诉帕金森症状,诊断为脑积水和药物诱导或血管性帕金森病)和神经对照组(10 例正常人和 8 例糖尿病性眼肌麻痹患者)时,PD 患者 CSF 中α-突触核蛋白寡聚体的水平仍明显高于两个对照组亚组。
这些发现进一步证实了α-突触核蛋白寡聚体的致病作用,并提示 CSF 中α-突触核蛋白寡聚体的水平可能是 PD 的可靠标志物。