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Abstract
We aimed to develop a novel prediction model for early neurological deterioration (END) based on an interpretable machine learning (ML) algorithm for atrial fibrillation (AF)-related stroke and to evaluate the prediction accuracy and feature importance of ML models. Data from multicenter prospective stroke registries in South Korea were collected. After stepwise data preprocessing, we utilized logistic regression, support vector machine, extreme gradient boosting, light gradient boosting machine (LightGBM), and multilayer perceptron models. We used the Shapley additive explanation (SHAP) method to evaluate feature importance. Of the 3,213 stroke patients, the 2,363 who had arrived at the hospital within 24 h of symptom onset and had available information regarding END were included. Of these, 318 (13.5%) had END. The LightGBM model showed the highest area under the receiver operating characteristic curve (0.772; 95% confidence interval, 0.715–0.829). The feature importance analysis revealed that fasting glucose level and the National Institute of Health Stroke Scale score were the most influential factors. Among ML algorithms, the LightGBM model was particularly useful for predicting END, as it revealed new and diverse predictors. Additionally, the effects of the features on the predictive power of the model were individualized using the SHAP method.
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1 Korea University College of Medicine, Department of Neurology, Korea University Ansan Hospital, Ansan-Si, South Korea (GRID:grid.222754.4) (ISNI:0000 0001 0840 2678)
2 Korea University College of Medicine, Department of Neurology, Korea University Anam Hospital, Seoul, South Korea (GRID:grid.222754.4) (ISNI:0000 0001 0840 2678)
3 Korea University College of Medicine, Department of Neurology, Korea University Guro Hospital, Seoul, South Korea (GRID:grid.222754.4) (ISNI:0000 0001 0840 2678)
4 Ewha University College of Medicine, Department of Neurology, Seoul Hospital, Seoul, South Korea (GRID:grid.255649.9) (ISNI:0000 0001 2171 7754)
5 The Catholic University of Korea, Department of Neurology, Eunpyeong St. Mary’s Hospital, Seoul, Korea (GRID:grid.411947.e) (ISNI:0000 0004 0470 4224)
6 Kyung Hee University College of Medicine, Department of Neurology, Seoul, South Korea (GRID:grid.289247.2) (ISNI:0000 0001 2171 7818)
7 Chung-Ang University Hospital, Department of Neurology, Chung-Ang University College of Medicine, Seoul, South Korea (GRID:grid.411651.6) (ISNI:0000 0004 0647 4960)
8 Hanyang University Myongji Hospital Seoul, Department of Neurology, Seoul, South Korea (GRID:grid.49606.3d) (ISNI:0000 0001 1364 9317)
9 Jeju National University, Department of Neurology, Jeju, South Korea (GRID:grid.411277.6) (ISNI:0000 0001 0725 5207)
10 Chonnam National University Hospital, Department of Neurology, Chonnam, South Korea (GRID:grid.411597.f) (ISNI:0000 0004 0647 2471)
11 Chonnam National University Hwasun Hospital, Department of Neurology, Hwasun, South Korea (GRID:grid.411602.0) (ISNI:0000 0004 0647 9534)
12 Kyungpook National University Hospital, Department of Neurology, Dae-gu, South Korea (GRID:grid.411235.0) (ISNI:0000 0004 0647 192X)
13 University of Ulsan College of Medicine, Department of Neurology, Asan Medical Center, Seoul, South Korea (GRID:grid.267370.7) (ISNI:0000 0004 0533 4667)
14 Samsung Medical Center, Department of Neurology and Stroke Center, Seoul, South Korea (GRID:grid.414964.a) (ISNI:0000 0001 0640 5613)
15 Korea University College of Medicine, Department of Neurology, Korea University Ansan Hospital, Ansan-Si, South Korea (GRID:grid.222754.4) (ISNI:0000 0001 0840 2678); Korea University Zebrafish Translational Medical Research Center, Ansan, South Korea (GRID:grid.222754.4) (ISNI:0000 0001 0840 2678)