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Updated: Sep 4, 2025

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
Published on: January 31, 2022
DILI : An AI-Based Classifier to Search for Drug-Induced Liver Injury Literature
Sanjay Rathee1, Meabh MacMahon1,2, Anika Liu1,3
1Milner Therapeutics Institute, University of Cambridge, Cambridge, United Kingdom.
Abstract:
Drug-induced liver injury (DILI) is a class of adverse drug reactions (ADR) that causes problems in both clinical and research settings. It is the most frequent cause of acute liver failure in the majority of Western countries and is a major cause of attrition of novel drug candidates. Manual trawling of the literature is the main route of deriving information on DILI from research studies. This makes it an inefficient process prone to human error. Therefore, an automatized AI model capable of retrieving DILI-related articles from the huge ocean of literature could be invaluable for the drug discovery community. In this study, we built an artificial intelligence (AI) model combining the power of natural language processing (NLP) and machine learning (ML) to address this problem. This model uses NLP to filter out meaningless text (e.g., stop words) and uses customized functions to extract relevant keywords such as singleton, pair, and triplet. These keywords are processed by an apriori pattern mining algorithm to extract relevant patterns which are used to estimate initial weightings for a ML classifier. Along with pattern importance and frequency, an FDA-approved drug list mentioning DILI adds extra confidence in classification. The combined power of these methods builds a DILI classifier (DILI ), with 94.91% cross-validation and 94.14% external validation accuracy. To make DILI as accessible as possible, including to researchers without coding experience, an R Shiny app capable of classifying single or multiple entries for DILI is developed to enhance ease of user experience and made available at https://researchmind.co.uk/diliclassifier/. Additionally, a GitHub link (https://github.com/sanjaysinghrathi/DILI-Classifier) for app source code and ISMB extended video talk (https://www.youtube.com/watch?v=j305yIVi_f8) are available as supplementary materials.
Insights
An AI model accurately identifies drug-induced liver injury (DILI) from research literature, improving drug discovery. This tool aids researchers by automating DILI article retrieval, reducing errors and saving time.
Area of Science:
- Biomedical Informatics
- Pharmacology
- Artificial Intelligence
Background:
- Drug-induced liver injury (DILI) is a significant cause of acute liver failure and drug development attrition.
- Current methods for identifying DILI from literature are manual, inefficient, and prone to human error.
- Automated retrieval of DILI information is crucial for the drug discovery community.
Purpose of the Study:
- To develop an automated artificial intelligence (AI) model for efficient retrieval of DILI-related research articles.
- To enhance the accuracy and speed of identifying potential drug-induced liver injury cases from scientific literature.
Main Methods:
- Utilized natural language processing (NLP) for text filtering and keyword extraction (singletons, pairs, triplets).
- Employed an apriori pattern mining algorithm to identify relevant patterns for machine learning (ML) classification.
- Integrated pattern importance, frequency, and FDA-approved drug lists to train and validate the DILI classifier.
Main Results:
- Developed a DILI classifier (DILI) achieving 94.91% cross-validation accuracy.
- Attained 94.14% accuracy on external validation datasets.
- Created an accessible R Shiny app for user-friendly DILI classification of single or multiple entries.
Conclusions:
- The AI-powered DILI classifier significantly improves the efficiency and accuracy of identifying drug-induced liver injury from scientific literature.
- The developed R Shiny application provides a valuable, accessible tool for researchers, including those without coding expertise.
- This automated approach supports the drug discovery process by streamlining the identification of potential DILI risks.
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