使用改进的遗传算法发现心血管事件风险分层的生物标志物

Xiaobo Thou, Honghui Wang, Jun Wang, G. Hoehn, J. Azok, M. Brennan, S. Hazen, King C. Li, Stephen T. C. Wong
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引用次数: 14

摘要

检测一组能够预测患者主要心脏不良事件(MACE)风险的最佳生物标志物具有临床意义。由于人体血液中蛋白质浓度的高动态范围,应用蛋白质组学技术进行蛋白质分析可以产生大量数据,用于开发优化的临床生物标志物面板。本研究的目的是发现一组生物标志物,以可靠地预测受试者的MACE风险。免疫测定的发展只能容忍少于10个选定的生物标志物的预测模型的复杂性。因此,传统的优化方法,如遗传算法,无法在这样的高维空间中推导出解。在本文中,我们提出了一种改进的遗传算法,结合局部浮动搜索技术来发现具有改进预后价值的生物标志物子集,用于预测MACE。通过MACE预测实验,将该方法与标准遗传算法和其他特征选择方法进行了比较
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomarker Discovery for Risk Stratification of Cardiovascular Events using an Improved Genetic Algorithm
Detection of an optimal panel of biomarkers capable of predicting a patient's risk of major adverse cardiac events (MACE) is of clinical significance. Due to the high dynamic range of the protein concentration in human blood, applying proteomics techniques for protein profiling can generate large arrays of data for development of optimized clinical biomarker panels. The objective of this study is to discover a panel of biomarkers for predicting risk of MACE in subjects reliably. The development of immunoassay can only tolerate the complexity of the prediction model with less than ten selected biomarkers. Hence, traditional optimization methods, such as genetic algorithm, cannot be used to derive a solution in such a high-dimensional space. In this paper, we propose an improved genetic algorithm with the local floating searching technique to discover a subset of biomarkers with improved prognostic values for prediction of MACE. The proposed method has been compared with standard genetic algorithm and other feature selection approaches based on the MACE prediction experiments
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