Department of Psychiatry, University of Oxford, UK.
Maurice Wohl Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK.
J Alzheimers Dis. 2020;74(1):213-225. doi: 10.3233/JAD-190434.
We have previously investigated, discovered, and replicated plasma protein biomarkers for use to triage potential trials participants for PET or cerebrospinal fluid measures of Alzheimer's disease (AD) pathology. This study sought to undertake validation of these candidate plasma biomarkers in a large, multi-center sample collection. Targeted plasma analyses of 34 proteins with prior evidence for prediction of in vivo pathology were conducted in up to 1,000 samples from cognitively healthy elderly individuals, people with mild cognitive impairment, and in patients with AD-type dementia, selected from the EMIF-AD catalogue. Proteins were measured using Luminex xMAP, ELISA, and Meso Scale Discovery assays. Seven proteins replicated in their ability to predict in vivo amyloid pathology. These proteins form a biomarker panel that, along with age, could significantly discriminate between individuals with high and low amyloid pathology with an area under the curve of 0.74. The performance of this biomarker panel remained consistent when tested in apolipoprotein E ɛ4 non-carrier individuals only. This blood-based panel is biologically relevant, measurable using practical immunocapture arrays, and could significantly reduce the cost incurred to clinical trials through screen failure.
我们之前已经研究、发现和复制了用于对潜在试验参与者进行 PET 或脑脊液阿尔茨海默病(AD)病理测量的分诊的血浆蛋白生物标志物。本研究旨在在一个大型的多中心样本集中对这些候选血浆生物标志物进行验证。对来自认知健康老年人、轻度认知障碍患者和 AD 型痴呆患者的多达 1000 个样本进行了具有预测体内病理证据的 34 种蛋白质的靶向血浆分析,这些患者选自 EMIF-AD 目录。使用 Luminex xMAP、ELISA 和 Meso Scale Discovery 测定法测量蛋白质。有 7 种蛋白质能够复制其预测体内淀粉样蛋白病理的能力。这些蛋白质形成了一个生物标志物面板,与年龄一起,可以显著区分具有高和低淀粉样蛋白病理的个体,曲线下面积为 0.74。当仅在载脂蛋白 Eɛ4 非携带者中进行测试时,该生物标志物面板的性能保持一致。该基于血液的面板具有生物学相关性,可使用实用的免疫捕获阵列进行测量,并可通过筛选失败显著降低临床试验的成本。