Breath Signatures of Antiseizure Medication Response and Tolerability in Adults With Epilepsy
Kai Fricke, Diego Manuel Baur, Kapil Dev Singh, Felix Schmidt, Kathrin Müsch, Noriane Andrina Sievi, Marco Di Donato, Anton Schmick, Silvia Ulrich, Pablo Sinues, Marian Galovic, Malcolm KohlerABSTRACT
Purpose
Achieving seizure control without intolerable adverse effects remains a major challenge in adult epilepsy, and serum concentrations of antiseizure medications correlate poorly with clinical outcomes. Metabolic processes influencing treatment response are not captured by blood monitoring. This study evaluates whether exhaled breath metabolomic profiles reflect treatment response and adverse effects in adults receiving antiseizure therapy, using epilepsy as a model for pharmacodynamic phenotyping.
Materials and Methods
A single‐center observational cohort of 117 adults provided 127 breath samples during stable antiseizure treatment. Exhaled breath samples were analyzed using secondary electrospray ionization high‐resolution mass spectrometry. Machine‐learning models with nested cross‐validation were used to classify treatment response and adverse effects, and pathway‐level analyses were performed to provide biological context. Findings were compared with an independent, predominantly pediatric cohort analyzed using the same workflow.
Results
Breath metabolomic profiles distinguished responders from nonresponders and individuals with and without adverse effects, whereas serum drug concentrations showed no meaningful association. Classification models achieved areas under the curve of 0.84 for treatment response and 0.88 for adverse effects, with good calibration. Pathway‐level alterations were directionally consistent across cohorts.
Conclusion
Breath metabolomics supports a non‐invasive approach to pharmacodynamic phenotyping that captures treatment‐related metabolic states not reflected by serum drug concentrations.