DJ-1 和α-突触核蛋白在人脑脊液中作为帕金森病的生物标志物。
DJ-1 and alpha-synuclein in human cerebrospinal fluid as biomarkers of Parkinson's disease.
机构信息
Department of Pathology, University of Washington School of Medicine, HMC Box 359635, 325 9th Avenue, Seattle, WA 98104, USA.
出版信息
Brain. 2010 Mar;133(Pt 3):713-26. doi: 10.1093/brain/awq008. Epub 2010 Feb 15.
Biomarkers are urgently needed for the diagnosis and monitoring of disease progression in Parkinson's disease. Both DJ-1 and alpha-synuclein, two proteins critically involved in Parkinson's disease pathogenesis, have been tested as disease biomarkers in several recent studies with inconsistent results. These have been largely due to variation in the protein species detected by different antibodies, limited numbers of patients in some studies, or inadequate control of several important variables. In this study, the nature of DJ-1 and alpha-synuclein in human cerebrospinal fluid was studied by a combination of western blotting, gel filtration and mass spectrometry. Sensitive and quantitative Luminex assays detecting most, if not all, species of DJ-1 and alpha-synuclein in human cerebrospinal fluid were established. Cerebrospinal fluid concentrations of DJ-1 and alpha-synuclein from 117 patients with Parkinson's disease, 132 healthy individuals and 50 patients with Alzheimer's disease were analysed using newly developed, highly sensitive Luminex technology while controlling for several major confounders. A total of 299 individuals and 389 samples were analysed. The results showed that cerebrospinal fluid DJ-1 and alpha-synuclein levels were dependent on age and influenced by the extent of blood contamination in cerebrospinal fluid. Both DJ-1 and alpha-synuclein levels were decreased in Parkinson's patients versus controls or Alzheimer's patients when blood contamination was controlled for. In the population aged > or = 65 years, when cut-off values of 40 and 0.5 ng/ml were chosen for DJ-1 and alpha-synuclein, respectively, the sensitivity and specificity for patients with Parkinson's disease versus controls were 90 and 70% for DJ-1, and 92 and 58% for alpha-synuclein. A combination of the two markers did not enhance the test performance. There was no association between DJ-1 or alpha-synuclein and the severity of Parkinson's disease. Taken together, this represents the largest scale study for DJ-1 or alpha-synuclein in human cerebrospinal fluid so far, while using newly established sensitive Luminex assays, with controls for multiple variables. We have demonstrated that total DJ-1 and alpha-synuclein in human cerebrospinal fluid are helpful diagnostic markers for Parkinson's disease, if variables such as blood contamination and age are taken into consideration.
生物标志物对于帕金森病的诊断和疾病进展监测至关重要。DJ-1 和 alpha-突触核蛋白是两种与帕金森病发病机制密切相关的蛋白质,最近的几项研究已经将它们作为疾病生物标志物进行了测试,但结果不一致。这主要是由于不同抗体检测到的蛋白质种类不同、一些研究中的患者人数有限,或者几个重要变量的控制不足。在这项研究中,通过 Western blot、凝胶过滤和质谱联用的方法研究了 DJ-1 和 alpha-突触核蛋白在人脑脊液中的性质。建立了敏感和定量的 Luminex 检测法,可检测人脑脊液中 DJ-1 和 alpha-突触核蛋白的大多数(如果不是全部)种类。使用新开发的高灵敏度 Luminex 技术,在控制几个主要混杂因素的情况下,分析了来自 117 名帕金森病患者、132 名健康个体和 50 名阿尔茨海默病患者的脑脊液中 DJ-1 和 alpha-突触核蛋白的浓度。总共分析了 299 名个体和 389 个样本。结果表明,脑脊液 DJ-1 和 alpha-突触核蛋白水平与年龄有关,并受脑脊液中血液污染程度的影响。当控制血液污染时,与对照组或阿尔茨海默病患者相比,帕金森病患者的脑脊液 DJ-1 和 alpha-突触核蛋白水平降低。在年龄>或=65 岁的人群中,当分别选择 DJ-1 和 alpha-突触核蛋白的 40 和 0.5ng/ml 作为截断值时,DJ-1 和 alpha-突触核蛋白用于诊断帕金森病患者与对照组的敏感性和特异性分别为 90%和 70%,92%和 58%。两种标志物的组合并未提高检测性能。DJ-1 或 alpha-突触核蛋白与帕金森病的严重程度之间没有关联。总之,这是迄今为止针对人脑脊液中 DJ-1 或 alpha-突触核蛋白进行的最大规模研究,同时使用了新建立的敏感 Luminex 检测法,并对多个变量进行了控制。我们已经证明,如果考虑到血液污染和年龄等变量,脑脊液中的总 DJ-1 和 alpha-突触核蛋白是帕金森病的有用诊断标志物。