Interpretable multi-modality consensus QSAR framework: integrating machine and deep learning for enhanced multi-endpoint toxicity assessment

Accurate toxicity assessment is essential for chemical safety, but experimental testing is costly, slow, and ethically constrained, motivating the adoption of computational approaches such as quantitative structure-activity relationship (QSAR). However, many QSAR models still rely on a single descriptor type or algorithm and relatively small, endpoint‑specific datasets, which limits robustness, interpretability, and broader applicability. To overcome these limitations, this study develops an interpretable multi‑modality consensus QSAR framework that integrates multiple molecular representations with both machine learning (ML) and deep learning to predict eight mechanistically diverse toxicity endpoints - skin sensitization, respiratory toxicity, AMES mutagenicity, hepatotoxicity, developmental toxicity, cardiotoxicity, drug‑induced nephrotoxicity, and neurotoxicity - across 30 160 unique compounds. Models for each descriptor-algorithm combination were optimized using 10-fold cross-validation, and top-performing models were combined into weighted multi-modality consensus predictors based on cross-validated area under the receiver operating characteristic curve (AUC) weights. Across all endpoints, multi-modality consensus models consistently achieved moderate to excellent performance on unseen and external sets (AUC 0.80-0.99, balanced accuracy (BACC) 0.76-0.90). DeLong's test confirmed that multi-modality consensus models outperformed the best individual models, with significant AUC improvements (<i>p</i> < 0.05) in seven of eight endpoints. Chemical space and applicability domain analyses demonstrated broad coverage of diverse compounds, with in-domain predictions consistently achieving higher and more stable performance, while SHapley Additive exPlanations (SHAP) analysis highlighted global features and mechanistic-level motifs, supporting the model's biological plausibility and reliability. Overall, this multi-modality consensus framework provides a reliability aware and interpretable approach for broad-spectrum toxicity prediction and multi-endpoint chemical safety assessment.

Authors

Institutions

Publication Details

Journal
Toxicology Mechanisms and Methods
Published
2026-03-17
DOI
https://doi.org/10.1080/15376516.2026.2643659
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Interpretable multi-modality consensus QSAR framework: integrating machine and deep learning for enhanced multi-endpoint toxicity assessment

Muhammad Adnan Pramudito, Yunendah Nur Fuadah, Ki Moo Lim, Fauzan Syarif Nursyafi
Toxicology Mechanisms and Methods
Computational Drug Discovery Methods
article

Interpretable multi-modality consensus QSAR framework: integrating machine and deep learning for enhanced multi-endpoint toxicity assessment

Muhammad Adnan Pramudito, Yunendah Nur Fuadah, Ki Moo Lim, Fauzan Syarif Nursyafi
article en

Abstract

Accurate toxicity assessment is essential for chemical safety, but experimental testing is costly, slow, and ethically constrained, motivating the adoption of computational approaches such as quantitative structure-activity relationship (QSAR). However, many QSAR models still rely on a single descriptor type or algorithm and relatively small, endpoint‑specific datasets, which limits robustness, interpretability, and broader applicability. To overcome these limitations, this study develops an interpretable multi‑modality consensus QSAR framework that integrates multiple molecular representations with both machine learning (ML) and deep learning to predict eight mechanistically diverse toxicity endpoints - skin sensitization, respiratory toxicity, AMES mutagenicity, hepatotoxicity, developmental toxicity, cardiotoxicity, drug‑induced nephrotoxicity, and neurotoxicity - across 30 160 unique compounds. Models for each descriptor-algorithm combination were optimized using 10-fold cross-validation, and top-performing models were combined into weighted multi-modality consensus predictors based on cross-validated area under the receiver operating characteristic curve (AUC) weights. Across all endpoints, multi-modality consensus models consistently achieved moderate to excellent performance on unseen and external sets (AUC 0.80-0.99, balanced accuracy (BACC) 0.76-0.90). DeLong's test confirmed that multi-modality consensus models outperformed the best individual models, with significant AUC improvements (<i>p</i> < 0.05) in seven of eight endpoints. Chemical space and applicability domain analyses demonstrated broad coverage of diverse compounds, with in-domain predictions consistently achieving higher and more stable performance, while SHapley Additive exPlanations (SHAP) analysis highlighted global features and mechanistic-level motifs, supporting the model's biological plausibility and reliability. Overall, this multi-modality consensus framework provides a reliability aware and interpretable approach for broad-spectrum toxicity prediction and multi-endpoint chemical safety assessment.

Toxicology Mechanisms and Methods
Kumoh National Institute of Technology (KR), Heart Foundation (US), Telkom University (ID)
Openalex Percentile: Top 18%
Computational Drug Discovery Methods
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.