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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Use of Saliva-Based Nano-Biochip Tests for Acute Myocardial Infarction at the Point of Care: A Feasibility Study
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Use of Saliva-Based Nano-Biochip Tests for Acute Myocardial Infarction at the Point of Care: A Feasibility Study

机译:基于唾液的纳米生物芯片测试在护理点对急性心肌梗死的可行性研究

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Background: For adults with chest pain, the electrocardiogram (ECG) and measures of serum biomarkers are used to screen and diagnose myocardial necrosis. These measurements require time that can delay therapy and affect prognosis. Our objective was to investigate the feasibility and utility of saliva as an alternative diagnostic fluid for identifying biomarkers of acute myocardial infarction (AMI).Methods: We used Luminex and lab-on-a-chip methods to assay 21 proteins in serum and unstimulated whole saliva procured from 41 AMI patients within 48 h of chest pain onset and from 43 apparently healthy controls. Data were analyzed by use of logistic regression and area under curve (AUC) for ROC analysis to evaluate the diagnostic utility of each biomarker, or combinations of biomarkers, in screening for AMI.Results: Both established and novel cardiac biomarkers demonstrated significant differences in concentrations between patients with AMI and controls without AMI. The saliva-based biomarker panel of C-reactive protein, myoglobin, and myeloperoxidase exhibited significant diagnostic capability (AUC = 0.85, P 0.0001) and in conjunction with ECG yielded strong screening capacity for AMI (AUC = 0.96) comparable to that of the panel (brain natriuretic peptide, troponin-I, creatine kinase-MB, myoglobin; AUC = 0.98) and far exceeded the screening capacity of ECG alone (AUC approximately 0.6). En route to translating these findings to clinical practice, we adapted these unstimulated whole saliva tests to a novel lab-on-a-chip platform for proof-of-principle screens for AMI.Conclusions: Complementary to ECG, saliva-based tests within lab-on-a-chip systems may provide a convenient and rapid screening method for cardiac events in prehospital stages for AMI patients.
机译:背景:对于患有胸痛的成年人,心电图(ECG)和血清生物标志物的测定可用于筛查和诊断心肌坏死。这些测量需要时间,可能会延迟治疗并影响预后。我们的目的是研究唾液作为替代诊断液鉴别急性心肌梗死(AMI)生物标志物的可行性和实用性。方法:我们使用Luminex和芯片实验室方法测定了血清中21种蛋白质和未刺激的整体蛋白质在胸痛发作后48小时内从41名AMI患者和43名显然健康的对照中获得唾液。通过逻辑回归和曲线下面积(AUC)进行ROC分析来分析数据,以评估每种生物标志物或生物标志物组合在筛查AMI中的诊断效用。结果:既有的和新型的心脏生物标志物均显示出浓度的显着差异在患有AMI的患者和没有AMI的对照组之间。 C反应蛋白,肌红蛋白和髓过氧化物酶的基于唾液的生物标志物组显示出显着的诊断能力(AUC = 0.85,P <0.0001),并且与ECG结合使用可产生与AMI相当的强大AMI筛查能力(AUC = 0.96)。图(脑利钠肽,肌钙蛋白-I,肌酸激酶-MB,肌红蛋白; AUC = 0.98),远远超出了单独ECG的筛查能力(AUC约为0.6)。在将这些发现转化为临床实践的过程中,我们将未经刺激的整个唾液测试改编为一个新型的芯片实验室平台,用于AMI的原理验证筛选。结论:与ECG互补,实验室内基于唾液的测试片上系统可以为AMI患者的院前阶段的心脏事件提供一种便捷的快速筛查方法。

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