Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at University of Gothenburg, Mölndal, Sweden.
PLoS One. 2013 Jun 14;8(6):e66381. doi: 10.1371/journal.pone.0066381. Print 2013.
The current study evaluated amyloid-β oligomers (Aβo) in cerebrospinal fluid as a clinical biomarker for Alzheimer's disease (AD). We developed a highly sensitive Aβo ELISA using the same N-terminal monoclonal antibody (82E1) for capture and detection. CSF samples from patients with AD, mild cognitive impairment (MCI), and healthy controls were examined. The assay was specific for oligomerized Aβ with a lower limit of quantification of 200 fg/ml, and the assay signal showed a tight correlation with synthetic Aβo levels. Three clinical materials of well characterized AD patients (n = 199) and cognitively healthy controls (n = 148) from different clinical centers were included, together with a clinical material of patients with MCI (n = 165). Aβo levels were elevated in the all three AD-control comparisons although with a large overlap and a separation from controls that was far from complete. Patients with MCI who later converted to AD had increased Aβo levels on a group level but several samples had undetectable levels. These results indicate that presence of high or measurable Aβo levels in CSF is clearly associated with AD, but the overlap is too large for the test to have any diagnostic potential on its own.
本研究评估了脑脊液中的淀粉样蛋白-β寡聚体(Aβo)作为阿尔茨海默病(AD)的临床生物标志物。我们使用相同的 N 端单克隆抗体(82E1)进行捕获和检测,开发了一种高灵敏度的 Aβo ELISA。检测了 AD、轻度认知障碍(MCI)和健康对照组患者的 CSF 样本。该测定法对寡聚化 Aβ具有特异性,定量下限为 200 fg/ml,测定信号与合成 Aβo 水平密切相关。该研究纳入了三个临床资料良好的 AD 患者(n=199)和认知健康对照组(n=148),以及一个 MCI 患者的临床资料(n=165)。虽然存在很大的重叠,但 Aβo 水平在所有三个 AD-对照组比较中均升高,与对照组的分离也远未完全。后来发展为 AD 的 MCI 患者的 Aβo 水平在组水平上升高,但有几个样本的水平无法检测到。这些结果表明,CSF 中存在高水平或可测量的 Aβo 水平与 AD 明显相关,但重叠太大,仅凭该检测无法具有任何诊断潜力。