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Metabolomics-Based Study of Clinical and Animal Plasma Samples in Coronary Heart Disease with Blood Stasis Syndrome

机译:基于代谢组学的冠心病合并血瘀证的血浆和动物血浆研究

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摘要

The aim of this study is to explore a bridge connecting the mechanism basis and macro syndromes of coronary heart disease with experimental animal models. GC-MS technique was used to detect the metabolites of plasma samples in mini swine models with myocardial infarction (MI) and patients with unstable angina (UA). 30 metabolites were detected in the plasma samples of more than 50 percent of model group and control group in swine, while 37 metabolites were found in the plasma samples of UA patients and healthy control group. 21 metabolites in the plasma samples of swine model and 20 metabolites in patients with UA were found of significant value. Among which, 8 shared metabolites were found of low level expression in both swine model and UA patients. Independent Student's t-test, principal component analysis (PCA), and hierarchicalcluster analysis (HCA) were orderly applied to comprehend inner rules of variables in the data. The 8 shared metabolites could take place of the 21 or 20 metabolites in classification of swine model with MI and UA patients, which could be considered as a bridge connecting the mechanism basis and macrosyndromes of swine model with MI and UA patients.
机译:这项研究的目的是探索连接冠状动脉心脏病的机理基础和宏观综合症与实验动物模型的桥梁。使用GC-MS技术检测患有心肌梗塞(MI)的小型猪模型和不稳定型心绞痛(UA)患者的血浆样品中的代谢物。在模型组和对照组的50%以上的猪血浆中检测到30种代谢物,而在UA患者和健康对照组的血浆中发现37种代谢物。猪模型血浆样品中有21种代谢物,UA患者中有20种代谢物具有重要价值。其中,在猪模型和UA患者中发现8种共有的代谢产物低水平表达。独立学生的t检验,主成分分析(PCA)和层次聚类分析(HCA)被有序地应用于理解数据中变量的内部规则。在MI和UA患者的猪模型分类中,这8种共有代谢物可以代替21或20种代谢物,这可以看作是将MI和UA患者的猪模型的机理基础和宏观综合征连接起来的桥梁。

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