El-Agnaf Omar M A, Salem Sultan A, Paleologou Katerina E, Curran Martin D, Gibson Mark J, Court Jennifer A, Schlossmacher Michael G, Allsop David
Department of Biochemistry, Faculty of Medicine and Health Science, United Arab Emirates University, Al Ain P. O. Box 17666, United Arab Emirates.
FASEB J. 2006 Mar;20(3):419-25. doi: 10.1096/fj.03-1449com.
To date there is no accepted clinical diagnostic test for Parkinson's disease (PD) based on biochemical analysis of blood or cerebrospinal fluid (CSF). alpha-Synuclein (alpha-syn) protein has been linked to the pathogenesis of PD with the discovery of mutations in the gene encoding alpha-syn in familial cases with early-onset PD. Lewy bodies and Lewy neurites, which constitute the main pathological features in the brains of patients with sporadic PD and dementia with Lewy bodies, are formed by the conversion of soluble monomers of alpha-syn into insoluble aggregates. We recently reported the presence of alpha-syn in normal human blood plasma and in postmortem CSF. Here, we investigated whether alpha-syn can be used as a biomarker for PD. We have developed a novel ELISA method that detects only oligomeric "soluble aggregates" of alpha-syn. Using this ELISA, we report the presence of significantly elevated (P=0.002) levels of oligomeric forms of alpha-syn in plasma samples obtained from 34 PD patients compared with 27 controls; 52% (95% confidence intervals 0.353-0.687) of the PD patients displayed signals >0.5 OD with our ELISA assay in comparison to only 14.8% (95% confidence intervals 0.014-0.281) for the control cases. An analysis of the test's diagnostic value revealed a specificity of 0.852 (95% confidence intervals 0.662-0.958), sensitivity of 0.529 (95% confidence intervals 0.351-0.702) and a positive predictive value of 0.818 (95% confidence intervals 0.597-0.948). These observations offer new opportunities for developing diagnostic tests for PD and related diseases and for testing therapeutic agents aimed at preventing or reversing the aggregation of alpha-syn.
迄今为止,尚无基于血液或脑脊液(CSF)生化分析的被广泛认可的帕金森病(PD)临床诊断检测方法。随着早发性PD家族病例中编码α-突触核蛋白(α-syn)的基因突变的发现,α-突触核蛋白与PD的发病机制相关联。路易小体和路易神经突是散发性PD患者和路易体痴呆患者大脑中的主要病理特征,它们由α-syn的可溶性单体转化为不溶性聚集体形成。我们最近报道了正常人血浆和死后CSF中存在α-syn。在此,我们研究了α-syn是否可作为PD的生物标志物。我们开发了一种新型酶联免疫吸附测定(ELISA)方法,该方法仅检测α-syn的寡聚“可溶性聚集体”。使用这种ELISA,我们报告了与27名对照相比,从34名PD患者获得的血浆样本中α-syn寡聚体形式的水平显著升高(P = 0.002);与对照病例仅14.8%(95%置信区间0.014 - 0.281)相比,52%(95%置信区间0.353 - 0.687)的PD患者在我们的ELISA检测中显示信号>0.5 OD。对该检测诊断价值的分析显示特异性为0.852(95%置信区间0.662 - 0.958),敏感性为0.529(95%置信区间0.351 - 0.702),阳性预测值为0.818(95%置信区间0.597 - 0.948)。这些观察结果为开发PD及相关疾病的诊断检测方法以及测试旨在预防或逆转α-syn聚集的治疗药物提供了新机会。