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Integrated action crossing method for Drug-Drug Interactions prediction in noncommunicable diseases based on neural networks

机译:基于神经网络的非传染性疾病中药物 - 药物相互作用预测的综合动作交叉方法

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Drug-Drug Interactions (DDI) is a cause of treatment inefficacy and toxicity. The most DDI involve drug metabolism which related to enzyme and transporter protein. Drug-enzyme actions that alter the metabolism of other drugs consist of substrate, inhibitor and inducer. Non-communicable diseases (NCDs) are the leading cause of death, drugs that are used in NCDs can increase interaction probability because their long-term usage. This paper proposes Integrated Action Crossing (IAC), a new attribute generation method for DDIs prediction in NCDs. Drugs attributes in NCDs categories were extracted. The actions of enzymes and transporter proteins were crossed for generating dataset for prediction model creation. Neural network (NN) and others machine learning were investigated. Five-fold cross validation was performed for evaluaing the prediction model performance. The results showed that 2 layers NN obtained the best performance of NCDs DDIs prediction model at the accuracy of 83.15%.
机译:药物 - 药物相互作用(DDI)是治疗的原因低效率和毒性。 大多数DDI涉及与酶和转运蛋白有关的药物代谢。 改变其他药物代谢的药物 - 酶作用包括底物,抑制剂和诱导剂。 非传染性疾病(NCDS)是死亡的主要原因,在NCD中使用的药物可以增加互动概率,因为它们的长期使用。 本文提出了NCD中DDIS预测的新属性生成方法的综合动作交叉(IAC)。 提取了NCDS类别中的药物属性。 酶和转运蛋白的作用被交叉以产生用于预测模型的数据集。 研究了神经网络和其他机器学习。 对评估预测模型性能进行五倍的交叉验证。 结果表明,2层NN以83.15%的准确度获得了NCDS DDIS预测模型的最佳性能。

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