A novel machine learning model based on sparse structure learning with adaptive graph regularization for predicting drug side effects.
Drug side effects are closely related to the success and failure of drug development. Here we present a novel machine learning method for side effect prediction. The proposed method treats side effect prediction as a multi-label learning problem and uses sparse structure learning to model the relati...
| Publicado en: | Journal of Biomedical Informatics Vol. 132 |
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| Autores principales: | , , , , , |
| Formato: | research Journal Article |
| Publicado: |
Academic Press Inc.
Aug2022
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=158403803&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 158403803 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 15320464 OMB jtl: Journal of Biomedical Informatics issn: 15320464 maglogo: N pubinfo: dt: Aug2022 vid: 132 pid: 735 pub: Academic Press Inc. place: Burlington, Massachusetts artinfo: ui: 158403803 158403803 NLM35840061 158403803 10.1016/j.jbi.2022.104131 NLM35840061 158403803 ppct: 1 formats: tig: atl: A novel machine learning model based on sparse structure learning with adaptive graph regularization for predicting drug side effects. aug: au: Liang, Xujun Li, Jun Fu, Ying Qu, Lingzhi Tan, Yuying Zhang, Pengfei affil: NHC Key Laboratory of Cancer Proteomics, Department of Oncology, PR China sug: subj: Adverse Drug Event Study Design Algorithms Human ab: Drug side effects are closely related to the success and failure of drug development. Here we present a novel machine learning method for side effect prediction. The proposed method treats side effect prediction as a multi-label learning problem and uses sparse structure learning to model the relationships between side effects. Additionally, the proposed method adopts the adaptive graph regularization strategy to explore the local structure in drug data and fuse multiple types of drug features. An alternating optimization algorithm is proposed to solve the optimization problem. We collected chemical structures and biological pathway features of drugs as the inputs of our method to predict drug side effects. The results of the cross-validation experiment showed that our method could significantly improve the prediction performance compared to the other state-of-the-art methods. Besides, our model is highly interpretable. It could learn the drug neighbourhood relationships, side effect relationships, and drug features related to side effects. We systematically validated the information extracted by the model with independent data. Some prediction results could also be supported by literature reports. The proposed method could be applied to integrate both chemical and biological data to predict side effects and helps improve drug safety. pubtype: Academic Journal doctype: research Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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