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冠状动脉疾病中的尿液蛋白质组学生物标志物

Urinary proteomic biomarkers in coronary artery disease.

作者信息

Zimmerli Lukas U, Schiffer Eric, Zürbig Petra, Good David M, Kellmann Markus, Mouls Laetitia, Pitt Andrew R, Coon Joshua J, Schmieder Roland E, Peter Karlheinz H, Mischak Harald, Kolch Walter, Delles Christian, Dominiczak Anna F

机构信息

British Heart Foundation (BHF) Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow G12 8TA, United Kingdom.

出版信息

Mol Cell Proteomics. 2008 Feb;7(2):290-8. doi: 10.1074/mcp.M700394-MCP200. Epub 2007 Oct 19.

Abstract

Urinary proteomics is emerging as a powerful non-invasive tool for diagnosis and monitoring of variety of human diseases. We tested whether signatures of urinary polypeptides can contribute to the existing biomarkers for coronary artery disease (CAD). We examined a total of 359 urine samples from 88 patients with severe CAD and 282 controls. Spot urine was analyzed using capillary electrophoresis on-line coupled to ESI-TOF-MS enabling characterization of more than 1000 polypeptides per sample. In a first step a "training set" for biomarker definition was created. Multiple biomarker patterns clearly distinguished healthy controls from CAD patients, and we extracted 15 peptides that define a characteristic CAD signature panel. In a second step, the ability of the CAD-specific panel to predict the presence of CAD was evaluated in a blinded study using a "test set." The signature panel showed sensitivity of 98% (95% confidence interval, 88.7-99.6) and 83% specificity (95% confidence interval, 51.6-97.4). Furthermore the peptide pattern significantly changed toward the healthy signature correlating with the level of physical activity after therapeutic intervention. Our results show that urinary proteomics can identify CAD patients with high confidence and might also play a role in monitoring the effects of therapeutic interventions. The workflow is amenable to clinical routine testing suggesting that non-invasive proteomics analysis can become a valuable addition to other biomarkers used in cardiovascular risk assessment.

摘要

尿液蛋白质组学正逐渐成为一种用于诊断和监测多种人类疾病的强大非侵入性工具。我们测试了尿液多肽特征是否有助于现有的冠状动脉疾病(CAD)生物标志物。我们共检测了来自88例重度CAD患者和282例对照的359份尿液样本。使用与电喷雾电离飞行时间质谱联用的毛细管电泳分析随机尿样,每个样本可鉴定1000多种多肽。第一步,创建用于生物标志物定义的“训练集”。多种生物标志物模式可清晰区分健康对照与CAD患者,我们提取了15种肽,它们定义了一个特征性的CAD特征组。第二步,在一项盲法研究中,使用“测试集”评估CAD特异性组预测CAD存在的能力。该特征组显示出98%的敏感性(95%置信区间,88.7 - 99.6)和83%的特异性(95%置信区间,51.6 - 97.4)。此外,治疗干预后,肽模式朝着与体力活动水平相关的健康特征显著变化。我们的结果表明,尿液蛋白质组学能够高度准确地识别CAD患者,并且可能在监测治疗干预效果方面发挥作用。该工作流程适用于临床常规检测,这表明非侵入性蛋白质组学分析可以成为心血管风险评估中其他生物标志物的有价值补充。

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