Deep Learning-Based Classification of Apical Hypertrophic Cardiomyopathy Using Left Ventricular Opacification and Enhanced LV Apex Imaging.

INTRODUCTION Accurate classification of apical hypertrophic cardiomyopathy (ApHCM) subtypes is challenging due to morphological variability and overlapping phenotypes. Conventional echocardiography provides limited visualization of the apex. Artifacts induced during left ventricular opacification (LVO) complicate diagnostic interpretation. A deep learning-based framework enhances image quality and improves subtype classification.

Materials And Methods

In this work, a deep learning-based framework is used for ApHCM subtype classification. Apical four-chamber end-diastolic frames from 3,200 individual patients were extracted from the EchoNet-Dynamic Dataset. Two cardiology experts manually annotated images into pure ApHCM, relative ApHCM, mixed ApHCM, and normal classes, based on apical wall thickness and morphological characteristics, using a computer vision annotation tool. A deep learning pipeline integrated multilevel graph-based adaptive particle swarm optimization with a deep denoised convolutional neural network (MG-APSO-DnCNN) to suppress reverberation and clutter artifacts from LVO echocardiograms. Enhanced images were then segmented using a U-Net-based levelset model to delineate the left ventricular (LV) apex. Morphological and LV wall features were extracted from the segmented region, and a graph isomorphism network (GIN) was trained to capture both local hypertrophic patterns and global ventricular morphology for subtype classification. The framework was designed to distinguish among pure ApHCM, relative ApHCM, and mixed ApHCM.

Results

The framework achieved a classification accuracy of 96.2%, with a precision, recall, and F1-score of approximately 95%. Cross-validation results indicate stable performance (95.8% ± 0.4%, p < 0.001), and ablation experiments confirmed the contribution of each pipeline component.

Discussion

By combining denoising, segmentation, and graph-based learning, the framework addressed limitations caused by LVO artifacts and improved the recognition of subtle ApHCM subtypes. These results demonstrate the clinical potential of integrating morphological feature extraction with deep learning in echocardiography.

Conclusion

The framework integrating MG-APSO-DnCNN and GIN enables accurate and robust ApHCM subtype classification, supporting cardiologists in early diagnosis, patient risk stratification, and treatment planning.