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A Novel Feature Selection Method to Choose Protein Biomarkers for CHD

机译:一种选择冠心病蛋白质生物标志物的新特征选择方法

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Coronary heart disease is now a severe burden on society and family in both industrialized and developing countries, but the traditional related factors can not explain the whole situations. The effect of treatment is very limited. Determination of treatment based on the symptoms and signs in Traditional Chinese Medicine (TCM) have certain curative effect. But the objective of the syndrome diagnose is a very urgent and difficult problem in TCM. Under the foundation work we had done, the aim of this study was to search for a novel feature selection method for the chose of protein biomarkers for unstable angina (UA) with blood stasis syndrome. Plasma samples were obtained from twenty-four unstable angina patients and twelve healthy volunteers. A polyclonal antibody affinity column was used to remove the six most abundant proteins. Then, the two classes of samples were separated by Twodimensional difference gel electrophoresis (2D-DIGE). The differentially expressed protein spots were selected and identified with matrix-assisted laser desorption /ionization time-of-flight mass spectrometry (MALDI-TOF-MS) or MS-MS. Using multilayer perceptron, we choose the protein biomarkers for UA with blood stasis syndrome. By using a back elimination method integrated with classification methods, it is found that the optimal number of proteins is six, i.e., α1-Antitrypsin 2, HP cleaved β, α1Antitrypsin, ApoA-I, DBP4, Fg β 2. The proteins are biomarkers to separate UA with blood stasis syndrome from health control. The UA with blood stasis syndrome diagnosis accuracy could reach 96%. The obtained patterns are validated by 3-fold cross validation. The multi-layer perceptron may be a useful novel feature selection method for the choosing of protein biomarkers for CHD.
机译:在工业化国家和发展中国家,冠心病现在已成为社会和家庭的沉重负担,但是传统的相关因素并不能解释整个情况。治疗效果非常有限。根据症状和体征确定治疗方法在中医(TCM)中有一定疗效。但是,中医对症候群的诊断是一个非常紧迫而又困难的问题。在我们所做的基础工作下,本研究的目的是寻找一种新的特征选择方法,以选择具有血瘀综合征的不稳定型心绞痛(UA)的蛋白质生物标志物。从二十四名不稳定型心绞痛患者和十二名健康志愿者获得血浆样品。多克隆抗体亲和柱用于去除六个最丰富的蛋白质。然后,通过二维差异凝胶电泳(2D-DIGE)分离两类样品。选择差异表达的蛋白质斑点,并通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)或MS-MS进行鉴定。使用多层感知器,我们选择具有血瘀综合征的UA的蛋白质生物标志物。通过与分类方法相结合的反向消除方法,发现蛋白质的最佳数目为6种,即α1-抗胰蛋白酶2,HP裂解的β,α1抗胰蛋白酶,ApoA-I,DBP4,Fgβ2。将具有血瘀综合征的UA与健康控制区分开来。血瘀证的UA诊断准确率可达96%。通过三重交叉验证来验证所获得的模式。多层感知器可能是一种有用的新颖的特征选择方法,用于选择CHD的蛋白质生物标志物。

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