Predicting drug-induced liver injury: The importance of data curation

被引:51
作者
Kotsampasakou, Eleni [1 ]
Montanari, Floriane [1 ]
Ecker, Gerhard F. [1 ]
机构
[1] Univ Vienna, Dept Pharmaceut Chem, Althanstr 14, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
Drug-induced liver injury; Random Forest; 2-class classification; Liver transporters; Data curation; Toxicity reports; IN-VITRO INHIBITION; HUMAN HEPATOTOXICITY; ABC TRANSPORTERS; MODELS; RISK; HEPATOBILIARY; DISPOSITION; METABOLISM; PHARMACEUTICALS; IDENTIFICATION;
D O I
10.1016/j.tox.2017.06.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug-induced liver injury (DILI) is a major issue for both patients and pharmaceutical industry due to insufficient means of prevention/prediction. In the current work we present a 2-class classification model for DILI, generated with Random Forest and 2D molecular descriptors on a dataset of 966 compounds. In addition, predicted transporter inhibition profiles were also included into the models. The initially compiled dataset of 1773 compounds was reduced via a 2-step approach to 966 compounds, resulting in a significant increase (p-value < 0.05) in model performance. The models have been validated via 10-fold cross-validation and against three external test sets of 921, 341 and 96 compounds, respectively. The final model showed an accuracy of 64% (AUC 68%) for 10-fold cross-validation (average of 50 iterations) and comparable values for two test sets (AUC 59%, 71% and 66%, respectively). In the study we also examined whether the predictions of our in-house transporter inhibition models for BSEP, BCRP, P-glycoprotein, and OATP1B1 and 1B3 contributed in improvement of the DILI mode. Finally, the model was implemented with open-source 2D RDKit descriptors in order to be provided to the community as a Python script.
引用
收藏
页码:139 / 145
页数:7
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