4.6 Article

DILI-Stk: An Ensemble Model for the Prediction of Drug-induced Liver Injury of Drug Candidates

Journal

CURRENT BIOINFORMATICS
Volume 17, Issue 3, Pages 296-303

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1574893617666211228113939

Keywords

Drug discovery; hepatotoxicity; machine learning; quantitative structure-activity relationship model; drug-induced liver injury; xenobiotics metabolism; xenobiotic metabolism

Funding

  1. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health and Welfare, Republic of Korea [HI21C1659]
  2. Chung-Ang University

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The study developed an ensemble model consisting of three high-performance DILI prediction models, which showed high predictive performance and is expected to provide a more reliable prediction model for drug discovery, reducing the rate of drug withdrawal.
Background: Drug-induced Liver Injury (DILI) is a leading cause of drug failure, accounting for nearly 20% of drug withdrawal. Thus, there has been a great demand for in silica DILI prediction models for successful drug discovery. To date, various models have been developed for DILI prediction; however, building an accurate model for practical use in drug discovery remains challenging. Methods: We constructed an ensemble model composed of three high-performance DILI prediction models to utilize the unique advantage of each machine learning algorithm. Results: The ensemble model exhibited high predictive performance, with an area under the curve of 0.88, sensitivity of 0.83, specificity of 0.77, F1-score of 0.82, and accuracy of 0.80. When a test dataset collected from the literature was used to compare the performance of our model with publicly available DILI prediction models, our model achieved an accuracy of 0.77, sensitivity of 0.82, specificity of 0.72, and F1-score of 0.79, which were higher than those of the other DILI prediction models. As many published DILI prediction models are not available for public access, which hinders in silico drug discovery, we made our DILI prediction model publicly accessible (http://ssbio.cau.ac.kr/software/dili/). Conclusion: We expect that our ensemble model may facilitate advancements in drug discovery by providing a highly predictive model and reducing the drug withdrawal rate.

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