计算机科学
嵌入
融合
情态动词
特征(语言学)
药品
人工智能
事件(粒子物理)
数据挖掘
算法
模式识别(心理学)
医学
物理
材料科学
哲学
语言学
量子力学
精神科
高分子化学
作者
Guishen Wang,Honghan Chen,Handan Wang,Hairong Gao,Xiaowen Hu,Chen Cao
标识
DOI:10.1109/jbhi.2025.3550019
摘要
Artificial intelligence techniques play a pivotal role in the accurate identification of drug-drug interaction (DDI) events, thereby informing clinical decisions and treatment regimens. While existing DDI prediction models have made significant progress by leveraging sequence features such as chemical substructures, targets, and enzymes, they often face limitations in integrating and effectively utilizing multi-modal drug representations. To address these limitations, this study proposes a novel multi-modal feature fusion model for DDI event prediction: MMDDI-SSE. Our approach integrates drug sequence modality with DDI graph representations through a novel architecture that employs static subgraph generation to capture structural properties. The model utilizes a graph autoencoder architecture to learn both local and global topological features from these subgraphs, while simultaneously processing diverse sequence-based characteristics including semantically enhanced pharmacodynamic features, chemical substructures, target proteins, and enzyme information. Through comprehensive evaluation on two distinct datasets, MMDDI-SSE demonstrates superior predictive performance compared to state-of-the-art baselines. Ablation studies further validate the effectiveness of each architectural component in enhancing DDI prediction accuracy.
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