AI-enhanced emulators identified sex-specific QT prolongation thresholds for loperamide, predicting mean absolute errors below 4 ms in risk assessment.
Can an AI-enhanced framework integrating high-fidelity electrophysiology simulations with machine-learning emulators predict sex-specific QT prolongation and arrhythmic risk from loperamide overexposure?
AI-driven emulators trained on mechanistic electrophysiology models can rapidly and accurately predict sex-specific drug-induced QT prolongation, enhancing preclinical cardiac safety assessments.
Absolute Event Rate: 0% vs 0%
Abstract Background Drug-induced QT interval prolongation remains a leading indicator of proarrhythmic risk and a major challenge in cardiac safety pharmacology. While regulatory guidelines (ICH S7B/E14) call for improved non-clinical methods 2, mechanistic in silico models offer a powerful yet underused tool for early safety evaluation. Purpose This work aims to present an AI-enhanced framework that integrates high-fidelity electrophysiology simulations with machine-learning–based emulators to assess drug-induced QT prolongation in a sex-specific manner. Methods Sex-specific virtual populations were generated using 3D finite-element cardiac electrophysiology models 1, simulating drug effects via a multi-channel pore-block model across key ion currents. From these simulations, pseudo-ECGs were extracted to quantify QT changes. To enable rapid risk evaluation, we developed Gaussian Process Regression emulators trained on over 900 3D simulations 3. These emulators allow real-time predictions of QT prolongation with uncertainty quantification, achieving mean absolute errors below 4 ms. Results As a proof of concept, we applied this framework to loperamide, a drug associated with abuse-related cardiotoxicity. The emulators were used to explore a wide concentration range beyond therapeutic exposure, identifying thresholds of arrhythmic risk across male and female profiles. Figure 1 illustrates the relationship between total concentration and QT prolongation (ΔQT), highlighting sex-specific risk thresholds and arrhythmic outcomes. Conclusions This case study demonstrates how AI-driven emulators can extend the reach of mechanistic models to high-throughput safety assessment, even in scenarios that would be unethical or infeasible to test clinically. This framework supports more efficient and comprehensive drug safety evaluations.Predicted ΔQT under loperamide effect
Dominguez-Gomez et al. (Thu,) reported a other. AI-enhanced emulators identified sex-specific QT prolongation thresholds for loperamide, predicting mean absolute errors below 4 ms in risk assessment.