AI Article Synopsis

  • The timing of stroke onset is crucial for treatment, but identifying this in unknown onset strokes is challenging due to a lack of reliable methods, leading to inconsistent treatment choices.
  • Recent studies suggest that serum biomarkers may help in determining stroke onset time, but no effective specific biomarkers or methods currently exist for unknown onset strokes.
  • This study introduces a machine learning approach using XGBoost to analyze serum metabolites, successfully identifying five key metabolites that can detect acute ischemic stroke and estimate its onset time, which may have implications for clinical evaluations and treatment strategies despite being based on animal experiments.

Article Abstract

The time window from stroke onset is critical for the treatment decision. However, in unknown onset stroke, it is often difficult to determine the exact onset time because of the lack of assessment methods, which can result in controversial and random treatment decisions. Previous studies have shown that serum biomarkers, in addition to imaging assessment, are useful for determining the stroke onset time. However, as yet there are no specific biomarkers or corresponding methodologies that are accurate and effective for determining the onset time of unknown onset stroke. Herein, we describe our novel advanced metabolites-based machine learning method (termed extreme gradient boost [XGBoost]) combined with recursive feature elimination, which accurately screened five metabolites from 1124 metabolites detected in serum. These metabolites were capable of both detecting acute ischemic stroke and backtracking the acute ischemic stroke onset time. To further investigate the pathological mechanisms of acute ischemic stroke, we also examined characteristic metabolites in different brain regions, and found two metabolites that could distinguish the core infarct area from the ischemic penumbra. Although this study is based on animal experiments, our machine learning framework and selected metabolites may provide a basis for clinical stroke evaluation and treatment.

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http://dx.doi.org/10.1016/j.biopha.2022.113641DOI Listing

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