Department of Neurology Research, Beaumont Health System, Royal Oak, Michigan, USA.
PLoS One. 2012;7(12):e52285. doi: 10.1371/journal.pone.0052285. Epub 2012 Dec 17.
α-synuclein is thought to play a key role in Parkinson's disease (PD) because it is the major protein in Lewy bodies, and because its gene mutations, duplication, and triplication are associated with early-onset PD. There are conflicting reports as to whether serum and plasma concentrations of α-synuclein and anti-α-synuclein antibodies differ between PD and control subjects. The objectives of this study were to compare the levels of α-synuclein and its antibodies between individuals with typical PD (n=14), atypical Parkinson syndromes (n=11), idiopathic rapid eye movement sleep behavior disorder (n=10), and healthy controls (n=9), to assess the strength of association between these serum proteins, and to determine group sizes needed for a high probability (80% power) of detecting statistical significance for 25% or 50% differences between typical PD and control subjects for these measurements. Analysis of log-transformed data found no statistically significant differences between groups for either α-synuclein or its antibodies. The concentrations of these proteins were weakly correlated (Spearman rho=0.16). In subjects with typical PD and atypical Parkinson syndromes, anti-α-synuclein antibody levels above 1.5 µg/ml were detected only in subjects with no more than four years of clinical disease. Power analysis indicated that 236 and 73 samples per group would be required for an 80% probability that 25% and 50% differences, respectively, in mean α-synuclein levels between typical PD and control subjects would be statistically significant; for anti-α-synuclein antibodies, 283 and 87 samples per group would be required. Our findings are consistent with those previous studies which suggested that serum concentrations of α-synuclein and its antibodies are not significantly altered in PD.
α-突触核蛋白被认为在帕金森病(PD)中起关键作用,因为它是路易体中的主要蛋白,并且其基因突变、重复和三重复与早发性 PD 相关。关于 PD 和对照组之间血清和血浆中α-突触核蛋白和抗α-突触核蛋白抗体的浓度是否存在差异,存在相互矛盾的报告。本研究的目的是比较典型 PD(n=14)、非典型帕金森综合征(n=11)、特发性快速眼动睡眠行为障碍(n=10)和健康对照组(n=9)个体之间的α-突触核蛋白及其抗体水平,评估这些血清蛋白之间的关联强度,并确定需要多大的样本量才能有 80%的概率检测到这些测量值在典型 PD 和对照组之间的 25%或 50%差异具有统计学意义。对对数转换后的数据进行分析,发现各组之间的α-突触核蛋白或其抗体均无统计学差异。这些蛋白质的浓度呈弱相关(Spearman rho=0.16)。在典型 PD 和非典型帕金森综合征患者中,只有临床疾病不超过四年的患者才检测到抗α-突触核蛋白抗体水平高于 1.5µg/ml。功效分析表明,每组需要 236 和 73 个样本,才能有 80%的概率检测到典型 PD 和对照组之间平均α-突触核蛋白水平的 25%和 50%差异分别具有统计学意义;对于抗α-突触核蛋白抗体,每组需要 283 和 87 个样本。我们的研究结果与之前的研究一致,这些研究表明 PD 患者血清中α-突触核蛋白及其抗体的浓度没有明显改变。