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α-Synuclein and Anti-α-Synuclein Antibodies in Parkinson’s Disease, Atypical Parkinson Syndromes, REM Sleep Behavior Disorder, and Healthy Controls

机译:帕金森病,非典型帕金森综合征,REM睡眠行为障碍和健康对照中的α-突触核蛋白和抗α-突触核蛋白抗体

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摘要

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.
机译:人们认为,α-突触核蛋白在帕金森氏病(PD)中起关键作用,因为它是路易氏体中的主要蛋白质,并且其基因突变,重复和重复与早发性PD相关。关于PD和对照受试者之间α-突触核蛋白和抗α-突触核蛋白抗体的血清和血浆浓度是否存在矛盾的报道。这项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),个体之间的α-突触核蛋白及其抗体水平,和健康对照组(n = 9),以评估这些血清蛋白之间的结合强度,并确定高概率(80%功效)需要检测的典型PD与25%或50%差异的统计学显着性所需的组大小。对照对象进行这些测量。对数转换数据的分析发现,α-突触核蛋白或其抗体在两组之间没有统计学上的显着差异。这些蛋白质的浓度之间的相关性很弱(Spearman rho = 0.16)。在患有典型PD和非典型帕金森综合症的受试者中,仅在患有不超过四年临床疾病的受试者中检测到超过1.5 µg / ml的抗α-突触核蛋白抗体水平。功效分析表明,每组需要236和73个样本,才能有80%的概率,典型的PD和对照组之间的平均α-突触核蛋白水平分别有25%和50%的差异具有统计学意义;对于抗α-突触核蛋白抗体,每组需要283和87个样品。我们的发现与先前的研究一致,这些研究表明,PD中血清α-突触核蛋白及其抗体的浓度没有明显改变。

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