ArticleBriefings in bioinformatics2026
MHAFR-DDI: a multimodal hierarchical attention fusion and relation-aware architecture for drug-drug interaction event prediction.
Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Drug-drug interactions (DDIs) can lead to severe adverse reactions, and accurate prediction of DDI events is crucial for ensuring the safety of combination therapies and supporting drug development. Although deep learning-based approaches have achieved promising progress, existing models remain limited in modeling local-global dependencies, integrating multimodal information, and capturing cross-level molecular relationships. To address these challenges, we propose Multi-modal Hierarchical Attention Fusion and Relation-aware Architecture for DDI Event Prediction (MHAFR-DDI), a multimodal hierarchical attention fusion and relation-aware framework that enables unified modeling from intra-molecular representation to inter-molecular interaction. MHAFR-DDI adopts a two-stage pretraining-finetuning paradigm. In the pretraining stage, the model learns complementary representations from molecular sequences, 2D topological structures, and 3D spatial conformations, with modality-specific encoding mechanisms designed to capture both local structural characteristics and global semantic dependencies. Localized chemical primitives within each modality are first stabilized and then integrated into higher-level representations to ensure intra-modality stability and representational completeness. Subsequently, by introducing attention-guided data augmentation and multi-level contrastive learning, the model establishes alignment constraints across different modalities and their augmented views, thereby achieving cross-modal semantic consistency and effectively alleviating data sparsity. During the finetuning stage, the pretrained molecular representations are hierarchically fused and propagated over the drug-drug interaction graph, enabling interaction-aware information sharing among drugs and improving prediction reliability for rare drugs and long-tail interaction types. Experiments on benchmarks with 65 and 86 DDI types show that MHAFR-DDI outperforms state-of-the-art methods under the standard split, achieving macro-F1 gains of 9.5% and 6.7%, while remaining robust in weakly supervised long-tail and cold-start settings.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.