Key result
View-agnostic deep learning model identifies mitral valve prolapse with ~95% accuracy on multi-view echocardiography.
Why the study?
Traditional diagnostic methods for mitral valve prolapse phenotypes, specifically fibroelastic deficiency and Barlow's disease, have limitations that automated multi-view echocardiography approaches may address.
Does a view-agnostic deep neural network trained on multi-view echocardiographic sequences improve the diagnostic accuracy of classifying mitral valve prolapse phenotypes (Barlow's disease and fibroelastic deficiency)?
Observational (n=473)
No
Does a view-agnostic deep neural network trained on multi-view echocardiographic sequences improve the diagnostic accuracy of classifying mitral valve prolapse phenotypes (Barlow's disease and fibroelastic deficiency)?
A deep learning algorithm utilizing multi-view echocardiographic sequences can accurately and efficiently differentiate between mitral valve prolapse phenotypes, providing a feasible automated tool for evaluating valvular heart disease.
Supports automated MVP phenotyping on echocardiography; leaves open prospective validation before clinical use.
Aims: To address the limitations of traditional diagnostic methods for mitral valve prolapse (MVP), specifically fibroelastic deficiency (FED) and Barlow's disease (BD), by introducing an automated diagnostic approach utilizing multi-view echocardiographic sequences and deep learning. Methods and results: An echocardiographic data set, collected from Zhongshan Hospital, Fudan University, containing apical 2 chambers (A2C), apical 3 chambers (A3C), and apical 4 chambers (A4C) views, was employed to train the deep learning models. We separately trained view-specific and view-agnostic deep neural network models, which were denoted as MVP-VS and MVP view-agonistic (VA), for MVP diagnosis. Diagnostic accuracy, precision, sensitivity, F1-score, and specificity were evaluated for both BD and FED phenotypes. MVP-VS demonstrated an overall diagnostic accuracy of 0.94 for MVP. In the context of BD diagnosis, precision, sensitivity, F1-score, and specificity were 0.83, 1.00, 0.90, and 0.92, respectively. For FED diagnosis, the metrics were 1.00, 0.83, 0.91, and 1.00. MVP-VA exhibited an overall accuracy of 0.95, with BD-specific metrics of 0.85, 1.00, 0.92, and 0.94 and FED-specific metrics of 1.00, 0.83, 0.91, and 1.00. In particular, the MVP-VA model using mixed views for training demonstrated efficient diagnostic performance, eliminating the need for repeated development of MVP-VS models and improving the efficiency of the clinical pipeline by using arbitrary views in the deep learning model. Conclusion: This study pioneers the integration of artificial intelligence into MVP diagnosis and demonstrates the effectiveness of deep neural networks in overcoming the challenges of traditional diagnostic methods. The efficiency and accuracy of the proposed automated approach suggest its potential for clinical applications in the diagnosis of valvular heart disease.
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Wu et al. (2024) conducted an observational in Mitral Valve Prolapse (Barlow's disease and Fibroelastic deficiency) (n=473). Deep neural network (MVP-VA and MVP-VS models) vs. Expert echocardiographic diagnosis (Reference standard) was evaluated on Overall diagnostic accuracy for mitral valve prolapse. The view-agnostic deep neural network model (MVP-VA) using multi-view echocardiographic sequences achieved an overall diagnostic accuracy of 0.95 for identifying mitral valve prolapse.
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