Evidence map›Paper›PMID 39873945›Full record

ArticleInterdisciplinary sciences, computational life sciences2025

Adaptive Multi-Kernel Graph Neural Network for Drug-Drug Interaction Prediction.

Linqian Zhao, Junliang Shang, Xianghan Meng, Xin He, Yuanyuan Zhang, Jin-Xing Liu

Abstract read
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In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Linqian ZhaoSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Junliang ShangSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China. shangjunliang110@163.com.ORCID http://orcid.org/0000-0002-8488-2228
Xianghan MengSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Xin HeSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Yuanyuan ZhangSchool of Information and Control Engineering, Qingdao University of Technology, Qingdao, 266520, China.
Jin-Xing LiuSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.

Funding

National Natural Science Foundation of China 61972226National Natural Science Foundation of China 62172254National Natural Science Foundation of China 62472250
6 · The paper itself

Abstract

Combination therapy, which synergistically enhances treatment efficacy and inhibits disease progression through the combined effects of multiple drugs, has emerged as a mainstream approach for treating complex diseases and alleviating symptoms. However, drug-drug interactions (DDIs) can sometimes lead to adverse reactions, potentially endangering lives. Therefore, developing efficient and accurate DDI prediction methods is crucial for elucidating drug mechanisms and preventing side effects. Current prediction methods often focus solely on the presence of interactions between drugs when constructing DDI graphs, neglecting the specific types of DDIs. This oversight can result in a decline in predictive performance. To address this issue, we propose an Adaptive Multi-Kernel Graph Neural Network (AMKGNN) for DDI prediction. AMKGNN differentiates DDIs into increase-type and decrease-type interactions, constructing separate increased DDI and decreased DDI graphs as convolutional kernels. AMKGNN employs a graph kernel learning mechanism that adaptively determines the optimal threshold between high-frequency and low-frequency signals in the network to capture node embeddings. Initially, AMKGNN learns drug embedding representations based on these two graph convolutional kernels and various drug features. These representations are then concatenated and input into a deep neural network to predict potential DDIs. The results show that our model achieved AUC and AUPR values above 90% across three sub-tasks on two datasets, significantly outperforming the other five comparison models. Furthermore, ablation experiments and case studies validate the superiority of AMKGNN.

Indexed as

Neural Networks, ComputerAlgorithmsDrug InteractionsGraph Neural NetworksHumansAttention mechanismDeep learningDrug-drug interactionGraph neural networkGraph representation learning

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Registered trials

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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 OpenQuestion graph.