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Diagnosis of Cardiac Amyloidosis on Echocardiography Using Artificial Intelligence
Adam Ioannou1, Michel G Khouri2, Takeshi Kitai3
1National Amyloidosis Centre, University College London, Royal Free Campus, London, United Kingdom (A.I., J.M., A.S., L.V., Y.R., A.P., A.M.-N., M.U.R., H.L., P.N.H., A.W., J.D.G., M. Fontana).
Insights
Artificial intelligence (AI) improves cardiac amyloidosis (CA) diagnosis on echocardiography. An AI deep-learning model achieved 88.4% accuracy in external validation, outperforming traditional scoring systems for detecting CA.
Area of Science:
- Cardiology
- Medical Imaging
- Artificial Intelligence
Background:
- Diagnosing cardiac amyloidosis (CA) using echocardiography is challenging due to overlapping imaging features with other hypertrophic conditions.
- Existing multiparametric echocardiographic scoring systems require improvement for accurate CA detection.
Purpose of the Study:
- To evaluate artificial intelligence (AI)-derived measurements within existing echocardiographic scoring systems for CA detection.
- To develop and validate an AI-based deep-learning model for video-based CA diagnosis on echocardiography.
Main Methods:
- Utilized a large dataset of 5776 patients (2756 with CA, 3020 controls) from multiple international centers for training and validation.
- Developed a deep-learning model for video-based echocardiogram analysis and compared its performance against an AI-enhanced multiparametric score.
Main Results:
- The AI-enhanced multiparametric score achieved accuracies of 79.5% (US) and 79.7% (Japan).
- The AI deep-learning model demonstrated high internal accuracies (96.2%) and external validation accuracies (87.5% in US, 88.4% in Japan).
- The deep-learning model showed superior diagnostic performance (AUC, 0.93) compared to the AI-enhanced score (AUC, 0.88) and accurately differentiated CA from other hypertrophic phenocopies.
Conclusions:
- Both AI-derived measurements and the deep-learning model accurately identify CA across diverse global populations.
- The fully automated deep-learning model offers superior diagnostic accuracy for cardiac amyloidosis detection via echocardiography.
Background:
Diagnosing cardiac amyloidosis (CA) on echocardiography can be challenging due to the imaging overlap between CA and more prevalent causes of a hypertrophic phenotype. This study sought to (1) evaluate the performance of artificial-intelligence (AI) derived measurements incorporated into the established multiparametric echocardiographic scoring system to detect CA; (2) develop and validate an AI-based deep-learning model for video-based detection of CA on echocardiography.
Methods:
The study population comprised 5776 patients (CA, 2756; controls, 3020). The training data set included patients from the UK National Amyloidosis Center and Taiwan MacKay Memorial Hospital (CA, 2241; controls, 2130). External test data sets were obtained from the US Duke University Health System (CA, 334; left ventricular hypertrophy controls, 668) and Japan National Cerebral and Cardiovascular Center (CA, 181; left ventricular hypertrophy controls, 222).
Results:
The multiparametric echocardiographic score computed using AI-derived measurements achieved an accuracy of 79.5% (sensitivity, 75.4%; specificity, 81.5%) in the United States cohort and 79.7% (sensitivity, 81.6%; specificity, 78.1%) in the Japan cohort. The deep-learning model demonstrated accuracies of 96.2% (sensitivity, 96.8%; specificity, 95.7%) and 95.8% (sensitivity, 97.3%; specificity, 94.3%) in the internal validation and internal test sets, respectively. External validation of the deep-learning model showed accuracies of 87.5% (sensitivity, 86.6%; specificity, 87.9%) in the United States and 88.4% (sensitivity, 92.3%; specificity, 85.3%) in the Japanese cohort. Subgroup analysis demonstrated that the deep-learning model showed robust discrimination of CA from other hypertrophic phenocopies: CA versus hypertension (area under the curve [AUC], 0.92 [95% CI, 0.91-0.94]), CA versus hypertrophic cardiomyopathy (AUC, 0.91 [95% CI, 0.87-0.94]), CA versus aortic stenosis (AUC, 0.93 [95% CI, 0.90-0.95]), CA versus chronic kidney disease (AUC, 0.93 [95% CI, 0.91-0.95]). The deep-learning model was able to classify a greater proportion of patients compared with the AI-derived multiparametric echocardiographic score and achieved superior diagnostic accuracy (AUC, 0.93 [95% CI, 0.91-0.95] versus AUC, 0.88 [95% CI, 0.85-0.90]; P<0.001).
Conclusions:
Both the multiparametric echocardiographic score computed from AI-derived measurements and the fully automated deep-learning model can accurately identify patients with CA in globally diverse cohorts, with the deep-learning model providing superior performance.
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