Predicting Drug-Drug Interactions Using Meta-path Based Similarities

Farhan Tanvir, Muhammad Ifte Khairul Islam, Esra Akbas
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引用次数: 6

Abstract

Drug-drug interaction (DDI) indicates the event where a particular drug's desired course of action is modified when taken together with other drugs (s). DDIs may hamper, enhance, or reduce the expected effect of either drug or, at the worst possible scenario, cause an adverse side effect. While it is crucial to identify drug-drug interactions, it is quite impossible to detect all possible DDIs for a new drug during the clinical trial. Therefore, many computational methods are proposed for this task. In this paper, we propose a novel method, HIN-DDI for discovering DDIs. This method considers drugs and other biomedical entities like proteins, pathways, and side effects, for DDI prediction. We design a heterogeneous information network (HIN) to model relations between these entities. Afterward, we extract the rich semantic relationships among these entities using different meta-path-based topological features. An extensive set of features are fed to different classifiers for DDI prediction. Moreover, we run extensive experiments to compare and evaluate the effectiveness of HIN-DD I with other methods. Results exhibit that HIN-DDI is quite effective in predicting new drugs as well as existing drugs. Unlike existing works, HIN-DDI can predict new drugs, and more importantly, it can impressively outmatch baseline methods by up to 63%.
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使用基于元路径的相似性预测药物-药物相互作用
药物-药物相互作用(DDI)是指某一特定药物与其他药物一起服用时,其预期作用过程发生改变的事件。DDI可能会阻碍、增强或降低任何一种药物的预期效果,在最坏的情况下,还可能导致不良副作用。虽然确定药物-药物相互作用是至关重要的,但在临床试验期间,不可能检测到一种新药的所有可能的ddi。因此,针对这一任务提出了许多计算方法。本文提出了一种新的ddi发现方法——HIN-DDI。该方法考虑药物和其他生物医学实体,如蛋白质、途径和副作用,用于DDI预测。我们设计了一个异构信息网络(HIN)来建模这些实体之间的关系。然后,我们使用不同的基于元路径的拓扑特征提取这些实体之间丰富的语义关系。一组广泛的特征被馈送到不同的分类器进行DDI预测。此外,我们进行了大量的实验来比较和评估HIN-DD I与其他方法的有效性。结果表明,HIN-DDI对新药和现有药物的预测均有较好的效果。与现有的工作不同,HIN-DDI可以预测新药,更重要的是,它比基线方法高出63%。
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