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Validation of Plasma Proteomic Biomarkers Relating to Brain Amyloid Burden in the EMIF-Alzheimer’s Disease Multimodal Biomarker Discovery Cohort

机译:验证与EMIF-阿尔茨海默氏病多模式生物标志物发现队列中与脑淀粉样蛋白负荷有关的血浆蛋白质组学标志物

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摘要

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 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 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 4 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.
机译:我们之前已经研究,发现和复制了血浆蛋白生物标志物,用于对潜在的阿尔茨海默氏病(AD)病理PET或脑脊液测量试验参与者进行分类。这项研究试图对大型,多中心样本中的这些候选血浆生物标志物进行验证。从EMIF-AD目录中,从多达1,000名认知健康的老年个体,轻度认知障碍者和AD型痴呆患者中进行了多达1,000个样本的34种蛋白质的靶向血浆分析,这些样本具有预测病理的先兆。使用Luminex xMAP,ELISA和Meso Scale Discovery分析法测量蛋白质。七种蛋白质以预测淀粉样蛋白病理的能力复制。这些蛋白质形成了一个生物标志物组,随着年龄的增长,可以明显区分淀粉样蛋白病高低的个体,其曲线下面积为0.74。仅在载脂蛋白E 4非携带者个体中进行测试时,该生物标志物组的性能保持一致。这种基于血液的检测组具有生物学相关性,可以使用实用的免疫捕获阵列进行测量,并且可以显着降低因筛查失败而导致的临床试验费用。

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