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Improving Stroke Outcome Prediction Using Molecular and Machine Learning Approaches in Large Vessel Occlusion
Madhusmita Rout1, April Vaughan2, Evgeny V Sidorov2
1Department of Pediatrics, College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Insights
This study reveals that specific circulating miRNAs and metabolites can predict stroke outcomes in large vessel occlusion (LVO) patients. Integrating these molecular markers with clinical data significantly improves prediction accuracy for acute ischemic stroke (AIS).
Area of Science:
- Biomarkers
- Neuroscience
- Metabolomics
- Genomics
Background:
- Predicting stroke outcomes in acute ischemic stroke (AIS), particularly with large vessel occlusion (LVO), remains challenging.
- Current tools like infarct volume and NIHSS have limited accuracy for LVO patients.
- Blood-brain barrier (BBB) disruption in LVO may cause detectable metabolic and RNA changes.
Purpose of the Study:
- To determine if metabolic and RNA differences in circulation correlate with infarct size in LVO strokes.
- To assess if combining molecular markers with clinical/imaging data improves outcome prediction in LVO.
Main Methods:
- Infarct volume measured by MRI; 90-day outcomes assessed by modified Rankin Scale (mRS).
- Serum exosome microRNAs (miRNAs) analyzed via RNA sequencing.
- Metabolites identified using Nuclear Magnetic Resonance (NMR) spectroscopy.
Main Results:
- 41 miRNAs and 11 metabolites significantly associated with infarct volume.
- 8 miRNAs and ketone bodies correlated with infarct volume, NIHSS, and mRS.
- Machine learning integrating clinical, imaging, and omics data achieved 0.81 accuracy and 0.91 AUC for outcome prediction.
Conclusions:
- Molecular markers (miRNAs, metabolites) offer insights into stroke pathophysiology and outcome.
- Integrating omics data with clinical and imaging tools enhances predictive accuracy for LVO stroke.
- This approach provides a framework for improved stroke therapeutics and patient outcomes.
Abstract:
Introduction: Predicting stroke outcomes in acute ischemic stroke (AIS) can be challenging, especially for patients with large vessel occlusion (LVO). Available tools such as infarct volume and the National Institute of Health Stroke Scale (NIHSS) have shown limited accuracy in predicting outcomes for this specific patient population. The present study aimed to confirm whether sudden metabolic changes due to blood-brain barrier (BBB) disruption during LVO reflect differences in circulating metabolites and RNA between small and large core strokes. The second objective was to evaluate whether integrating molecular markers with existing neurological and imaging tools can enhance outcome predictions in LVO strokes. Methods: The infarction volume in patients was measured using magnetic resonance diffusion-weighted images, and the 90-day stroke outcome was defined by a modified Rankin Scale (mRS). Differential expression patterns of miRNAs were identified by RNA sequencing of serum-driven exosomes. Nuclear magnetic resonance (NMR) spectroscopy was used to identify metabolites associated with AIS with small and large infarctions. Results: We identified 41 miRNAs and 11 metabolites to be significantly associated with infarct volume in a multivariate regression analysis after adjusting for the confounders. Eight miRNAs and ketone bodies correlated significantly with infarct volume, NIHSS (severity), and mRS (outcome). Through integrative analysis of clinical, radiological, and omics data using machine learning, our study identified 11 top features for predicting stroke outcomes with an accuracy of 0.81 and AUC of 0.91. Conclusions: Our study provides a future framework for advancing stroke therapeutics by incorporating molecular markers into the existing neurological and imaging tools to improve predictive efficacy and enhance patient outcomes.
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