Predicting adverse drug effects: A heterogeneous graph convolution network with a multi-layer perceptron approach

被引:3
作者
Chen, Y-H [1 ,2 ]
Shih, Y-T [3 ]
Chien, C-S [3 ]
Tsai, C-S [4 ]
机构
[1] Taichung Tzu Chi Hosp, Dept Nephrol, Taichung, Taiwan
[2] Tzu Chi Univ, Sch Med, Hualien, Taiwan
[3] Natl Chung Hsing Univ, Dept Appl Math, Taichung, Taiwan
[4] Natl Chung Hsing Univ, Dept Management Informat Syst, Taichung, Taiwan
来源
PLOS ONE | 2022年 / 17卷 / 12期
关键词
IDENTIFICATION; VANCOMYCIN; ALGORITHM; MODELS; SYSTEM; SAFETY;
D O I
10.1371/journal.pone.0266435
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We apply a heterogeneous graph convolution network (GCN) combined with a multi-layer perceptron (MLP) denoted by GCNMLP to explore the potential side effects of drugs. Here the SIDER, OFFSIDERS, and FAERS are used as the datasets. We integrate the drug information with similar characteristics from the datasets of known drugs and side effect networks. The heterogeneous graph networks explore the potential side effects of drugs by inferring the relationship between similar drugs and related side effects. This novel in silico method will shorten the time spent in uncovering the unseen side effects within routine drug prescriptions while highlighting the relevance of exploring drug mechanisms from well-documented drugs. In our experiments, we inquire about the drugs Vancomycin, Amlodipine, Cisplatin, and Glimepiride from a trained model, where the parameters are acquired from the dataset SIDER after training. Our results show that the performance of the GCNMLP on these three datasets is superior to the non-negative matrix factorization method (NMF) and some well-known machine learning methods with respect to various evaluation scales. Moreover, new side effects of drugs can be obtained using the GCNMLP.
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页数:16
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