Computer and Control Engineering College, Qiqihar University, Qiqihar, 161006, China.
Sci Rep. 2024 Sep 27;14(1):22327. doi: 10.1038/s41598-024-71834-0.
The human microbiome plays a key role in drug development and precision medicine, but understanding its complex interactions with drugs remains a challenge. Identifying microbe-drug associations not only enhances our understanding of their mechanisms but also aids in drug discovery and repurposing. Traditional experiments are expensive and time-consuming, making computational methods for predicting microbe-drug associations a new trend. Currently, computational methods specifically designed for this task are still scarce. Therefore, to address the shortcomings of traditional experimental methods in predicting potential microbe-drug associations, this paper proposes a new prediction model named GCNATMDA. The model combines two deep learning models, Graph Convolutional Network and Graph Attention Network, and aims to reveal potential relationships between microbes and drugs by learning related features. Thus improve the efficiency and accuracy of prediction. We first integrated the microbe-drug association matrix from the existing dataset, and then combined the calculated microbe-drug characteristic matrix as the model input. The GCN module is used to dig deeper into the potential characterization of microbes and drugs, while the GAT module further learns the more complex interactions between them and generates the corresponding score matrix. The experimental results show that the GCNATMDA model achieves 96.59% and 93.01% in AUC and AUPR evaluation indexes, respectively, which is significantly better than the existing prediction models. In addition, the reliability of the prediction results is verified by a series of experiments.
人类微生物组在药物开发和精准医学中发挥着关键作用,但理解其与药物的复杂相互作用仍然是一个挑战。识别微生物-药物关联不仅可以增强我们对其机制的理解,还有助于药物发现和再利用。传统实验既昂贵又耗时,因此,用于预测微生物-药物关联的计算方法成为一种新趋势。目前,专门为此任务设计的计算方法仍然很少。因此,为了解决传统实验方法在预测潜在微生物-药物关联方面的缺点,本文提出了一种名为 GCNATMDA 的新预测模型。该模型结合了两种深度学习模型,即图卷积网络和图注意网络,旨在通过学习相关特征来揭示微生物和药物之间的潜在关系。从而提高预测的效率和准确性。我们首先整合了来自现有数据集的微生物-药物关联矩阵,然后将计算出的微生物-药物特征矩阵组合作为模型输入。GCN 模块用于更深入地挖掘微生物和药物的潜在特征,而 GAT 模块则进一步学习它们之间更复杂的相互作用,并生成相应的评分矩阵。实验结果表明,GCNATMDA 模型在 AUC 和 AUPR 评估指标上分别达到 96.59%和 93.01%,明显优于现有预测模型。此外,通过一系列实验验证了预测结果的可靠性。