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Identification of ischemic stroke risk in patients with left ventricular non-compaction using echocardiography, deep
Jiangtao Wang1, Wensheng Tao2,3, Zhenzhen Wang4
1Department of Ultrasound Medicine, The First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui, 241001, China.
Insights
A new model accurately predicts ischemic stroke (IS) risk in patients with left ventricular non-compaction (LVNC). This tool helps identify high-risk individuals for targeted prevention strategies.
Area of Science:
- Cardiology
- Medical Imaging
- Artificial Intelligence
Background:
- Left ventricular non-compaction (LVNC) is associated with ischemic stroke (IS).
- No current predictive models exist to assess IS risk in LVNC patients.
Purpose of the Study:
- To develop and validate a predictive model for assessing ischemic stroke risk in patients with left ventricular non-compaction.
Main Methods:
- A multicenter retrospective study involving 309 LVNC patients.
- Deep transfer learning (ResNet101) and radiomics features were extracted.
- A machine learning model (Res101-RAD-XGB) was constructed using LASSO and XGBoost.
Main Results:
- The Res101-RAD-XGB model demonstrated high predictive performance with AUCs of 0.942 (training), 0.913 (internal validation), and 0.921 (external validation).
- The model outperformed models using single feature types and existing clinical criteria.
Conclusions:
- The Res101-RAD-XGB model accurately identifies LVNC patients at risk for IS.
- This enables targeted preventive strategies for high-risk individuals.
Background:
There is a certain correlation between left ventricular non-compaction (LVNC) and ischemic stroke (IS); however, there are currently no predictive models available to assess the risk of IS in LVNC patients.
Methods:
A multicenter retrospective study included 309 LVNC patients from two institutions. Institution 1 (228 patients) provided a training and internal validation set, while institution 2 (81 patients) served as the external validation set. The deep transfer learning features were extracted using a ResNet101-based model, and the radiomics features were extracted using Pyradiomics. Feature selection was done with LASSO, the selected features were input into XGBoost to construct the Res101-RAD-XGB model. Model performance was evaluated using receiver operating characteristic (ROC) curves and decision curve analysis (DCA), and the model's interpretability was assessed using SHAP analysis and the Grad-CAM method. Finally, the performance of the Res101-RAD-XGB model was compared with that of clinical criteria to assess its effectiveness.
Results:
The Res101-RAD-XGB model achieved area under the curve (AUCs) of 0.942, 0.913, and 0.921 for the training, internal validation, and external validation sets, outperforming models using only one type of feature and clinical criteria.
Conclusion:
The Res101-RAD-XGB model can accurately identify LVNC patients who are at risk of IS, enabling specialists to develop targeted preventive strategies for high-risk individuals.
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