基于图神经网络的多药副作用预测元融合模型

Aggelos Ragkousis, Olga Flogera, V. Megalooikonomou
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引用次数: 0

摘要

尽管是治疗复杂疾病的一种非常流行的方法,但多药可导致不良副作用的风险增加,其中许多副作用是在药物投放市场后观察到的。幸运的是,观察到的不良副作用的数据可用性的显著增加为机器学习方法帮助预测副作用铺平了道路。在这项工作中,我们首先提出了一个用图神经网络进行多关系链接预测的新框架。给定一个多关系图,我们为图的每个节点创建特定于关系的向量表示。通过这种方法,我们通过将外部分子和蛋白质靶点信息与直接从药物-药物相互作用预测图生成的药物信息相结合,创建了具有副作用特异性的药物载体表示。使用我们的新元融合方法,每种信息类型由基于G神经网络的编码器架构产生,然后根据预测的副作用类型进行集成。虽然最先进的模型报告最大AUROC分数为0.91,但我们的技术达到了0.95分。此外,我们还表明,我们的融合方法为预测图中具有较小节点度的药物节点提供了有价值的外部知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MFSE: A Meta-Fusion Model for Polypharmacy Side-Effect Prediction with Graph Neural Networks
Despite being a very popular approach for treating complex diseases, polypharmacy can lead to increased risk of adverse side effects, many of which are observed after the drugs have been released in the market. Luckily, the significant increase in data availability of observed adverse side-effects has paved the way for machine learning approaches to assist in their prediction. In this work, we first present a novel framework for multi-relational link prediction with graph neural networks. Given a multi-relational graph, we create relation-specific vector representations for each node of the graph. With this approach, we create drug vector representations that are side-effect specific, by integrating external molecular and protein-target information with the drug information that is generated directly from the drug-drug interaction prediction graph. With our new meta-fusion approach, each information type is produced from a distinct G NN - based encoder architecture and then the integration is performed according to the side-effect type being predicted. While state-of-the-art models report maximum AUROC scores of 0.91, our technique reaches a score of 0.95. Also, we show that our fusion approach provides valuable external knowledge particularly to drug nodes in the prediction graph that have a smaller node degree.
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