Aug 2026· IEEE journal of biomedical and health informatics· Vol PP· 1 citation
Medicine
TL;DR
Experimental results show that CMAF-DDI improves multi-class DDI prediction compared with representative graph-based and multi-source fusion baselines and ablation, hyperparameter sensitivity, controlled protein perturbation, representation, and case-level analyses to examine the contribution and behavior of protein-enhanced cross-modal fusion.
Abstract
Accurate prediction of drug-drug interactions (DDIs) is crucial for medication safety and personalized treatment. Most existing methods primarily exploit molecular graphs or biomedical knowledge graphs, while target protein sequence information is often underused. This paper proposes CMAF-DDI, a multi-class DDI prediction framework that integrates protein sequence features, molecular graph features, and knowledge graph features. CMAF-DDI contains a bi-level cross-modal fusion module: an Attention Fusion (AF) level that models global dependencies among modalities using multi-head attention, and a Triple-feature Product Fusion (TPF) level that captures high-order cross-modal co-activation after projecting all modalities into a shared latent space. Experimental results on DrugBank and DRKG show that CMAF-DDI improves multi-class DDI prediction compared with representative graph-based and multi-source fusion baselines. We further provide ablation, hyperparameter sensitivity, controlled protein perturbation, representation, and case-level analyses to examine the contribution and behavior of protein-enhanced cross-modal fusion.
Experiments demonstrate that HSAF-DDI achieves superior overall performance compared to state-of-the-art methods, indicating the critical role of fine-grained biological features in improving the DDI prediction performance.
Xiaoli Lin, Si-Yuan Zhang, Bo Li et al.· Journal of Chemical Informat...· 0 citations
A novel multiview feature fusion-based graph representation model (MFF-GRM) for predicting DDI that integrates drug molecular graphs, SMILES sequences, DDI information networks, and drug biological features to learn drug features more comprehensively.
Mengyuan Jin, Dan Liu, E. Benfenati et al.· Applied intelligence (Boston...· 0 citations
This work establishes a principled paradigm shift toward reliability-aware multi-modal learning for drug discovery by performing integrated representation learning across multiple modalities, and proposes Cross-Modal Subspace Alignment (CMSA), which treats incomplete knowledge graphs as recoverable signals, synthesizin...
Xiaodong Zhu, Longjun Song, Shi-Ying Zeng et al.· IEEE journal of biomedical a...· 0 citations
IAMV-DDI is proposed, an interaction-aware multi-view molecular representation learning framework for DDI prediction and DDI event classification that achieves strong performance compared with representative network-based, chemical-structure-based, and hybrid baseline methods.
Huyen K. Nguyen, Quang H. Nguyen, D. Le· Journal of Chemical Informat...· 0 citations
DDI-MMAF is proposed, a lightweight cross-modal framework that avoids using explicit high-dimensional omics profiles as direct model inputs and enables accurate synergy prediction from raw minimalist inputs, offering a practical and efficient computational solution for cost-effective drug combination discovery.
Hao Li, Qianhui Jiang, Jiahui Guan et al.· European journal of medicina...· 0 citations
Results indicate that integrating heterogeneous structural cues through coarse- and fine-grained feature interaction provides an effective and scalable solution for DDI prediction.