TY - JOUR
T1 - Multimodal Artificial Intelligence for Cardiac Amyloidosis Diagnosis
T2 - Integrating Echocardiography With Clinical and Laboratory Data for Improved Detection
AU - Slivnick, Jeremy A.
AU - Lim, Sze Chi
AU - Randazzo, Michael
AU - Maurer, Mathew S.
AU - Helmke, Stephen
AU - Scherrer-Crosbie, Marielle
AU - Vakilpour, Azin
AU - Zareba, Karolina M.
AU - Goyal, Akash
AU - Cheng, Richard
AU - Nakamatsu, Nicole
AU - Kitano, Tetsuji
AU - Takeuchi, Masaaki
AU - Hotta, Viviane Tiemi
AU - Campos Vieira, Marcelo Luiz
AU - Elissamburu, Pablo
AU - Ronderos, Ricardo E.
AU - Prado, Aldo
AU - Koutroumpakis, Efstratios
AU - Deswal, Anita
AU - Pursnani, Amit
AU - Sarswat, Nitasha
AU - Addetia, Karima
AU - Cotella, Juan
AU - Ruberg, Frederick L.
AU - Frost, Matthew
AU - Fontana, Marianna
AU - Lam Su Ping, Carolyn
AU - Lang, Roberto M.
AU - Asch, Federico M.
N1 - Publisher Copyright:
© 2026 American Heart Association, Inc.
PY - 2026/6
Y1 - 2026/6
N2 - BACKGROUND: – Cardiac amyloidosis (CA) is an underdiagnosed yet treatable cause of heart failure in which timely diagnosis is essential to initiate life-prolonging therapies. While artificial intelligence (AI)-based tools using transthoracic echocardiography (TTE), electrocardiography, or electronic health records have demonstrated promise for CA detection, most rely on single data sources. We aimed to evaluate whether integrating clinical, laboratory, and TTE biomarkers improves the performance of an existing TTE-based AI model for CA detection. METHODS: – We developed and tested a combined AI echo-clinical model (AI-ECM) incorporating demographics, laboratory biomarkers, and TTE parameters into a previously validated TTE-only AI model (Us2.Ca). Model training and internal validation were performed using the Amyloidosis Imaging International Consortium, a global multiethnic registry comprised of 727 patients with CA and 316 controls, including 202 with suspected transthyretin-CA with negative diagnostic evaluation and 114 patients with biopsy-proven extracardiac light chain amyloidosis without cardiac involvement. Ground truth CA diagnosis was adjudicated per consensus criteria. AI-ECM and Us2.Ca performance was assessed using area under the curve, accuracy, sensitivity, and specificity. RESULTS: – In building the AI-ECM, feature importance analysis showed that having the Us2.Ca prediction scores, relative wall thickness, sex, and estimated glomerular filtration rate contributed most to performance. The AI-ECM demonstrated superior performance (area under the curve, 0.94; accuracy, 90%; sensitivity, 93%; specificity, 85%) compared with the Us2.Ca (area under the curve, 0.89; accuracy, 80%; sensitivity, 76%; specificity, 91%; P=0.006). While the Us2.Ca model classification was indeterminate in 9% of the cases, the AI-ECM allowed classification of all cases. The AI-ECM improved sensitivity for light chain-CA detection and maintained high accuracy across subtypes and control groups. CONCLUSIONS: – A multiparametric AI model integrating basic clinical, laboratory, and TTE data with the deep learning Us2.Ca improved performance for CA detection over Us2.Ca alone. This approach represents a step toward scalable, AI-guided precision diagnostics for CA in diverse populations.
AB - BACKGROUND: – Cardiac amyloidosis (CA) is an underdiagnosed yet treatable cause of heart failure in which timely diagnosis is essential to initiate life-prolonging therapies. While artificial intelligence (AI)-based tools using transthoracic echocardiography (TTE), electrocardiography, or electronic health records have demonstrated promise for CA detection, most rely on single data sources. We aimed to evaluate whether integrating clinical, laboratory, and TTE biomarkers improves the performance of an existing TTE-based AI model for CA detection. METHODS: – We developed and tested a combined AI echo-clinical model (AI-ECM) incorporating demographics, laboratory biomarkers, and TTE parameters into a previously validated TTE-only AI model (Us2.Ca). Model training and internal validation were performed using the Amyloidosis Imaging International Consortium, a global multiethnic registry comprised of 727 patients with CA and 316 controls, including 202 with suspected transthyretin-CA with negative diagnostic evaluation and 114 patients with biopsy-proven extracardiac light chain amyloidosis without cardiac involvement. Ground truth CA diagnosis was adjudicated per consensus criteria. AI-ECM and Us2.Ca performance was assessed using area under the curve, accuracy, sensitivity, and specificity. RESULTS: – In building the AI-ECM, feature importance analysis showed that having the Us2.Ca prediction scores, relative wall thickness, sex, and estimated glomerular filtration rate contributed most to performance. The AI-ECM demonstrated superior performance (area under the curve, 0.94; accuracy, 90%; sensitivity, 93%; specificity, 85%) compared with the Us2.Ca (area under the curve, 0.89; accuracy, 80%; sensitivity, 76%; specificity, 91%; P=0.006). While the Us2.Ca model classification was indeterminate in 9% of the cases, the AI-ECM allowed classification of all cases. The AI-ECM improved sensitivity for light chain-CA detection and maintained high accuracy across subtypes and control groups. CONCLUSIONS: – A multiparametric AI model integrating basic clinical, laboratory, and TTE data with the deep learning Us2.Ca improved performance for CA detection over Us2.Ca alone. This approach represents a step toward scalable, AI-guided precision diagnostics for CA in diverse populations.
KW - amyloidosis
KW - artificial intelligence
KW - biomarkers
KW - deep learning
KW - heart failure
KW - prealbumin
UR - https://www.scopus.com/pages/publications/105042293010
UR - https://www.scopus.com/pages/publications/105042293010#tab=citedBy
U2 - 10.1161/CIRCIMAGING.126.019610
DO - 10.1161/CIRCIMAGING.126.019610
M3 - Article
C2 - 42200278
AN - SCOPUS:105042293010
SN - 1941-9651
VL - 19
SP - e019610
JO - Circulation: Cardiovascular Imaging
JF - Circulation: Cardiovascular Imaging
IS - 6
ER -