Abstract

Prediction of adverse drug reactions is an important problem in drug discovery endeavors which can be addressed with data-driven strategies. SIDER is one of the most reliable and frequently used datasets for identification of key features as well as building machine learning models for side effects prediction. The inherently unbalanced nature of this data presents with a difficult multi-label multi-class problem towards prediction of drug side effects. We highlight the intrinsic issue with SIDER data and methodological flaws in relying on performance measures such as AUC while attempting to predict side effects.We argue for the use of metrics that are robust to class imbalance for evaluation of classifiers. Importantly, we present a ‘hierarchical anatomical classification schema’ which aggregates side effects into organs, sub-systems, and systems. With the help of a weighted performance measure, using 5-fold cross-validation we show that this strategy facilitates biologically meaningful side effects prediction at different levels of anatomical hierarchy. By implementing various machine learning classifiers we show that Random Forest model yields best classification accuracy at each level of coarse-graining. The manually curated, hierarchical schema for side effects can also serve as the basis of future studies towards prediction of adverse reactions and identification of key features linked to specific organ systems. Our study provides a strategy for hierarchical classification of side effects rooted in the anatomy and can pave the way for calibrated expert systems for multi-level prediction of side effects.

Highlights

  • Drugs produce a myriad of effects by virtue of their interactions with cellular mechanisms

  • A hierarchical anatomical classification schema for prediction of phenotypic side effects described at five different levels of concepts: System Organ Class (SOC), High Level Group Term (HLGT), High Level Term (HLT), Preferred Term (PT), and Lowest Level Term (LLT)

  • When seen from the perspective of drugs, the data were skewed with drugs that were presented with exceptionally large number of adverse reactions (Fig 3A)

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Summary

Introduction

Drugs produce a myriad of effects by virtue of their interactions with cellular mechanisms. Beyond their therapeutic effects, drugs are known to cause adverse reactions. Drugs are known to cause adverse reactions A hierarchical anatomical classification schema for prediction of phenotypic side effects hindered because of high attrition of candidate drugs due to adverse drug reactions. The complex nature of mechanisms involving interaction of drugs with cellular processes makes it challenging to model this phenomenon. Availability of empirical data of drug features and known side effects provides a basis for building data-driven models aimed at prediction of side effects

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