Department of Pathology, University of Washington School of Medicine, Seattle, WA 98104, USA.
Neurosci Lett. 2010 Aug 9;480(1):78-82. doi: 10.1016/j.neulet.2010.06.009. Epub 2010 Jun 9.
DJ-1 and alpha-synuclein are leading biomarkers for Parkinson's disease diagnosis and/or monitoring disease progression. A few recent investigations have determined DJ-1 and alpha-synuclein levels in plasma or serum, a more convenient sample source than cerebrospinal fluid; but the results were variable or even contradictory. Besides limitations in detection technology and limited number of cases in some studies, inadequate control of several important confounders likely has contributed to these inconsistent results. In this study, the relative contribution of each blood component to blood DJ-1 and alpha-synuclein was evaluated, followed by quantification of plasma levels of both markers in a larger cohort of patients/subjects ( approximately 300 cases) whose cerebrospinal fluid DJ-1 and alpha-synuclein levels have been determined recently. The results demonstrated that the DJ-1 and alpha-synuclein in blood resided predominantly in red blood cells (>95%), followed by platelets (1-4%), white blood cells and plasma (< or =1%), indicating that variations in hemolysis and/or platelet contamination could have a significant effect on plasma/serum DJ-1 and alpha-synuclein levels. Nonetheless, after adjusting for the age, although there was a trend of decrease in DJ-1 and alpha-synuclein in patients with Parkinson's or Alzheimer's disease compared with healthy controls, no statistical difference was observed in this cohort between any groups, even when the extent of hemolysis and platelet contamination were controlled for. Additionally, no correlation between DJ-1 or alpha-synuclein and Parkinson's disease severity was identified. In conclusion, unlike in cerebrospinal fluid, total DJ-1 or alpha-synuclein in plasma alone is not useful as biomarkers for Parkinson's disease diagnosis or progression/severity.
DJ-1 和 alpha-突触核蛋白是帕金森病诊断和/或监测疾病进展的主要生物标志物。一些最近的研究已经确定了血浆或血清中的 DJ-1 和 alpha-突触核蛋白水平,这是比脑脊液更方便的样本来源;但结果是可变的,甚至是矛盾的。除了检测技术的限制和一些研究中病例数量有限之外,一些重要混杂因素的控制不当可能导致了这些不一致的结果。在这项研究中,评估了每个血液成分对血液 DJ-1 和 alpha-突触核蛋白的相对贡献,然后在一个更大的患者/受试者队列中(约 300 例)定量测定了这两种标志物的血浆水平,这些患者/受试者的脑脊液 DJ-1 和 alpha-突触核蛋白水平最近已经确定。结果表明,血液中的 DJ-1 和 alpha-突触核蛋白主要存在于红细胞中(>95%),其次是血小板(1-4%)、白细胞和血浆(<或=1%),这表明溶血和/或血小板污染的变化可能对血浆/血清 DJ-1 和 alpha-突触核蛋白水平有显著影响。尽管如此,在调整年龄后,尽管与健康对照组相比,帕金森病或阿尔茨海默病患者的 DJ-1 和 alpha-突触核蛋白水平有下降趋势,但在这个队列中,任何组之间都没有观察到统计学差异,即使控制了溶血和血小板污染的程度。此外,在帕金森病患者中,DJ-1 或 alpha-突触核蛋白与疾病严重程度之间也没有相关性。总之,与脑脊液不同,血浆中总 DJ-1 或 alpha-突触核蛋白本身不能作为帕金森病诊断或进展/严重程度的生物标志物。