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Diagnosis of Coronary Heart Diseases Using Gene Expression Profiling; Stable Coronary Artery Disease Cardiac Ischemia with and without Myocardial Necrosis

机译:使用基因表达谱分析诊断冠心病;稳定的冠状动脉疾病有或没有心肌坏死的心脏缺血

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摘要

Cardiovascular disease (including coronary artery disease and myocardial infarction) is one of the leading causes of death in Europe, and is influenced by both environmental and genetic factors. With the recent advances in genomic tools and technologies there is potential to predict and diagnose heart disease using molecular data from analysis of blood cells. We analyzed gene expression data from blood samples taken from normal people (n = 21), non-significant coronary artery disease (n = 93), patients with unstable angina (n = 16), stable coronary artery disease (n = 14) and myocardial infarction (MI; n = 207). We used a feature selection approach to identify a set of gene expression variables which successfully differentiate different cardiovascular diseases. The initial features were discovered by fitting a linear model for each probe set across all arrays of normal individuals and patients with myocardial infarction. Three different feature optimisation algorithms were devised which identified two discriminating sets of genes, one using MI and normal controls (total genes = 6) and another one using MI and unstable angina patients (total genes = 7). In all our classification approaches we used a non-parametric k-nearest neighbour (KNN) classification method (k = 3). The results proved the diagnostic robustness of the final feature sets in discriminating patients with myocardial infarction from healthy controls. Interestingly it also showed efficacy in discriminating myocardial infarction patients from patients with clinical symptoms of cardiac ischemia but no myocardial necrosis or stable coronary artery disease, despite the influence of batch effects and different microarray gene chips and platforms.
机译:心血管疾病(包括冠状动脉疾病和心肌梗塞)是欧洲主要的死亡原因之一,并且受环境和遗传因素的影响。随着基因组学工具和技术的最新发展,利用血细胞分析中的分子数据可以预测和诊断心脏病。我们分析了从正常人(n = 21),非重大冠状动脉疾病(n = 93),不稳定型心绞痛(n = 16),稳定型冠状动脉疾病(n = 14)和心肌梗塞(MI; n = 207)。我们使用一种特征选择方法来识别一组基因表达变量,这些变量可以成功地区分不同的心血管疾病。通过为所有正常个体和患有心肌梗塞的患者中的每组探针拟合线性模型,发现了初始特征。设计了三种不同的特征优化算法,这些算法可识别两组可区分的基因,一组使用MI和正常对照(总基因= 6),另一组使用MI和不稳定型心绞痛患者(总基因= 7)。在所有分类方法中,我们都使用了非参数的k最近邻(KNN)分类方法(k = 3)。结果证明了最终特征集在区分心肌梗死患者和健康对照者方面的诊断稳健性。有趣的是,尽管分批作用和不同的微阵列基因芯片和平台的影响,它也显示出了区分心肌梗塞患者和具有心肌缺血但无心肌坏死或稳定冠状动脉疾病的临床症状的功效。

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  • 作者

    Nabila Kazmi; Tom R. Gaunt;

  • 作者单位
  • 年(卷),期 -1(11),3
  • 年度 -1
  • 页码 e0149475
  • 总页数 16
  • 原文格式 PDF
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