Department of Electronics and Information Engineering, Jeonbuk National University, Jeonju, 54896, South Korea.
Khalifa University Center for Autonomous Robotic Systems (KUCARS), Khalifa University, United Arab Emirates.
Comput Biol Med. 2024 Sep;179:108729. doi: 10.1016/j.compbiomed.2024.108729. Epub 2024 Jul 1.
Recent studies have illuminated the critical role of the human microbiome in maintaining health and influencing the pharmacological responses of drugs. Clinical trials, encompassing approximately 150 drugs, have unveiled interactions with the gastrointestinal microbiome, resulting in the conversion of these drugs into inactive metabolites. It is imperative to explore the field of pharmacomicrobiomics during the early stages of drug discovery, prior to clinical trials. To achieve this, the utilization of machine learning and deep learning models is highly desirable. In this study, we have proposed graph-based neural network models, namely GCN, GAT, and GINCOV models, utilizing the SMILES dataset of drug microbiome. Our primary objective was to classify the susceptibility of drugs to depletion by gut microbiota. Our results indicate that the GINCOV surpassed the other models, achieving impressive performance metrics, with an accuracy of 93% on the test dataset. This proposed Graph Neural Network (GNN) model offers a rapid and efficient method for screening drugs susceptible to gut microbiota depletion and also encourages the improvement of patient-specific dosage responses and formulations.
最近的研究揭示了人类微生物组在维持健康和影响药物药理反应方面的关键作用。涵盖约 150 种药物的临床试验揭示了与胃肠道微生物组的相互作用,导致这些药物转化为无活性的代谢物。在药物发现的早期阶段,即在临床试验之前,探索药物微生物组学领域至关重要。为此,强烈需要使用机器学习和深度学习模型。在这项研究中,我们提出了基于图的神经网络模型,即 GCN、GAT 和 GINCOV 模型,利用药物微生物组的 SMILES 数据集。我们的主要目标是对药物对肠道微生物群消耗的易感性进行分类。我们的结果表明,GINCOV 优于其他模型,在测试数据集上实现了令人印象深刻的性能指标,准确率达到 93%。所提出的图神经网络 (GNN) 模型为筛选易受肠道微生物群消耗影响的药物提供了一种快速有效的方法,也鼓励改善患者特异性剂量反应和配方。