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首页> 外文期刊>Nature biotechnology >A pipeline that integrates the discovery and verification of plasma protein biomarkers reveals candidate markers for cardiovascular disease
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A pipeline that integrates the discovery and verification of plasma protein biomarkers reveals candidate markers for cardiovascular disease

机译:整合血浆蛋白生物标志物发现和验证功能的管道揭示了心血管疾病的候选标志物

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摘要

We developed a pipeline to integrate the proteomic technologies used from the discovery to the verification stages of plasma biomarker identification and applied it to identify early biomarkers of cardiac injury from the blood of patients undergoing a therapeutic, planned myocardial infarction (PMI) for treatment of hypertrophic cardiomyopathy. Sampling of blood directly from patient hearts before, during and after controlled myocardial injury ensured enrichment for candidate biomarkers and allowed patients to serve as their own biological controls. LC-MS/MS analyses detected 121 highly differentially expressed proteins, including previously credentialed markers of cardiovascular disease and > 100 novel candidate biomarkers for myocardial infarction (MI). Accurate inclusion mass screening (AIMS) qualified a subset of the candidates based on highly specific, targeted detection in peripheral plasma, including some markers unlikely to have been identified without this step. Analyses of peripheral plasma from controls and patients with PMI or spontaneous MI by quantitative multiple reaction monitoring mass spectrometry or immunoassays suggest that the candidate biomarkers may be specific to MI. This study demonstrates that modern proteomic technologies, when coherently integrated, can yield novel cardiovascular biomarkers meriting further evaluation in large, heterogeneous cohorts.
机译:我们开发了一条管线,以整合从发现到血浆生物标志物鉴定的验证阶段所使用的蛋白质组学技术,并将其用于从接受治疗性计划性心肌梗死(PMI)的患者的血液中鉴定出心脏损伤的早期生物标志物,以治疗肥厚性心肌病。在受控的心肌损伤之前,之中和之后,直接从患者心脏中采集血液,以确保候选生物标记物的富集,并使患者可以作为自己的生物学对照。 LC-MS / MS分析检测到121种高度差异表达的蛋白质,其中包括先前已证明的心血管疾病标志物和100多种新的心肌梗死(MI)候选生物标志物。精确的包涵体质量筛选(AIMS)基于外周血浆中高度特异性的靶向检测,对候选物的一部分进行了鉴定,其中包括一些可能不经过此步骤即无法鉴定的标志物。通过定量多反应监测质谱或免疫测定法对来自对照组和患有PMI或自发性MI的患者的外周血浆进行分析,表明候选生物标志物可能对MI具有特异性。这项研究表明,当现代蛋白质组学技术紧密结合在一起时,可以产生新的心血管生物标志物,值得在大型,异质性队列研究中进一步评估。

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