Multi-label classification to predict antibiotic resistance from raw clinical MALDI-TOF mass spectrometry data

Antimicrobial resistance (AMR) poses a significant global health challenge, necessitating advanced predictive models to support clinical decision-making. In this study, we explore multi-label classification as a novel approach to predict antibiotic resistance across four clinically relevant bacteria...

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Veröffentlicht in:Scientific reports 2024-12, Vol.14 (1), p.31283-16, Article 31283
Hauptverfasser: Astudillo, César A., López-Cortés, Xaviera A., Ocque, Elias, Manríquez-Troncoso, José M.
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Sprache:eng
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Zusammenfassung:Antimicrobial resistance (AMR) poses a significant global health challenge, necessitating advanced predictive models to support clinical decision-making. In this study, we explore multi-label classification as a novel approach to predict antibiotic resistance across four clinically relevant bacteria: E. coli , S. aureus , K. pneumoniae , and P. aeruginosa . Using multiple datasets from the DRIAMS repository, we evaluated the performance of four algorithms – Multi-Layer Perceptron, Support Vector Classifier, Random Forest, and Extreme Gradient Boosting – under both single-label and multi-label frameworks. Our results demonstrate that the multi-label approach delivers competitive performance compared to traditional single-label models, with no statistically significant differences in most cases. The multi-label framework naturally captures the complex, interconnected nature of AMR data, reflecting real-world scenarios more accurately. We further validated the models on external datasets (DRIAMS B and C), confirming their generalizability and robustness. Additionally, we investigated the impact of oversampling techniques and provided a reproducible methodology for handling MALDI-TOF data, ensuring scalability for future studies. These findings underscore the potential of multi-label classification to enhance predictive accuracy in AMR research, offering valuable insights for developing diagnostic tools and guiding clinical interventions.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-024-82697-w