Predicting Drug-Drug Interactions Using Deep Neural Network

Xinyu Hou, Jiaying You, P. Hu
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引用次数: 8

Abstract

Drug-drug interactions (DDIs) can trigger unexpected pharmacological effects, including adverse drug events (ADEs), with causal mechanisms often unknown. Recently, deep neural network (DNN) models have achieved great success in many applications, including predicting pharmacological properties of drugs and drug repurposing. In this study, we generated features produced by SMILES (simplified molecular-input line-entry system) codes for more than 5,000 drugs downloaded from DrugBank. We built a deep neural network model to predict 80 DDI types using the features. We reached an overall accuracy and AUC (area under the curve) of receiver operating characteristic of 93.2% and 94.2% of the test data set and 94.9% and 95.6% of the validation data set, respectively. The trained model was applied to predict the DDI types of 13,155,885 drug-drug pairs combined by 5,130 drugs. The prediction results were applied to analyze the drugs currently used for treating inflammatory bowel disease (IBD). The potential drug combinations for treating IBD were discussed. These results can provide important insights on drug repurposing and guidelines during drug development.
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使用深度神经网络预测药物-药物相互作用
药物-药物相互作用(ddi)可引发意想不到的药理作用,包括药物不良事件(ADEs),其因果机制通常未知。近年来,深度神经网络(deep neural network, DNN)模型在预测药物的药理学性质和药物再利用等方面取得了巨大的成功。在这项研究中,我们为从DrugBank下载的5000多种药物生成了由SMILES(简化分子输入行输入系统)代码生成的特征。我们利用这些特征建立了一个深度神经网络模型来预测80种直拨类型。我们的总体准确度和曲线下面积(AUC)分别达到测试数据集的93.2%和94.2%,验证数据集的94.9%和95.6%。将训练好的模型应用于5130种药物组合的13155885对药物-药物对的DDI类型预测。预测结果被用于分析目前用于治疗炎症性肠病(IBD)的药物。讨论了治疗IBD的潜在药物组合。这些结果可以为药物开发过程中的药物再利用和指导提供重要的见解。
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