Tracking the Preclinical Progression of Transthyretin Amyloid Cardiomyopathy Using Artificial Intelligence-Enabled Electrocardiography and Echocardiography
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Background and Aims: The diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM) requires advanced imaging, precluding large-scale pre-clinical testing. Artificial intelligence (AI)-enabled transthoracic echocardiography (TTE) and electrocardiography (ECG) may provide a scalable strategy for pre-clinical monitoring. Methods: This was a retrospective analysis of individuals referred for nuclear cardiac amyloid testing at Yale-New Haven Health System (YNHHS, internal cohort) and Houston Methodist Hospitals (HMH, external cohort). Deep learning models trained to discriminate ATTR-CM from age/sex-matched controls on TTE videos (AI-Echo) and ECG images (AI-ECG) were deployed to generate study-level ATTR-CM probabilities (0-100%). Longitudinal trends in AI-derived probabilities were examined using age/sex-adjusted linear mixed models, and their discrimination of future disease was evaluated across preclinical stages. Results: Among 984 participants at YNHHS (median age 74 years, 44.3% female) and 806 at HMH (69 years, 34.5% female), 112 (11.4%) and 174 (21.6%) tested positive for ATTR-CM, respectively. Across cohorts and modalities, AI-derived ATTR-CM probabilities from 7,352 TTEs and 32,205 ECGs diverged as early as 3 years before diagnosis in cases versus controls ( p time(x)group interaction ≤ 0.004). Among those with both AI-Echo and AI-ECG available one-to-three years before nuclear testing (n=433 [YNHHS] and 174 [HMH]), a double-negative screen at a 0.05 threshold (164 [37.9%] and 66 [37.9%], vs all else) had 90.9% and 85.7% sensitivity (specificity of 40.3% and 41.2%), whereas a double-positive screen (78 [18.0%] and 26 [14.9%], vs all else) had 85.5% and 88.9% specificity (sensitivity of 60.6% and 42.9%). Conclusions: AI-enabled echocardiography and electrocardiography may enable scalable risk stratification of ATTR-CM during its pre-clinical course. Abstract Figure: Structured Graphical Abstract. Artificial intelligence (AI)-enhanced interpretation of standard echocardiographic videos and electrocardiographic (ECG) images may serve as digital biomarkers of disease progression during the early pre-clinical and clinical stages of transthyretin amyloid cardiomyopathy. We show that across two geographically distinct cohorts of individuals referred for nuclear cardiac amyloid testing, cases exhibit significantly faster progression in their AI-defined probabilities in the years before nuclear cardiac amyloid testing, compared with controls, a finding that was consistent across cohorts and modalities. These findings suggest that AI-enabled echocardiography and ECG may be able to identify those at risk for ATTR-CM up to 3 years before clinical diagnosis through standard clinical pathways. AI: artificial intelligence; ATTR-CM: transthyretin amyloid cardiomyopathy; ECG: electrocardiography; TTE: transthoracic echocardiography.
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The use of ECG images as input and a flexible strategy that allows for varying formats supports the scalability of the approach across resource settings.
“Moreover, the use of ECG images as the input, and a flexible strategy that allows for varying formats, supports the scalability of the approach across resources settings.38”
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Detection of Left Ventricular Systolic Dysfunction From Electrocardiographic Images
Sangha, V., Nargesi, A. A., Dhingra, L. S., Khunte, A., Mortazavi, B. J., Ribeiro, A. H., Banina, E., Adeola, O., Garg, N., Brandt, C. A., et al. (2023) · Circulation · doi:10.1161/circulationaha.122.062646 · Cited by 150 · see citing works
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- [1]Writing Committee, Kittleson MM, Ruberg FL, Ambardekar AV, Brannagan TH, Cheng RK, 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis: A Report of the AmericanCollege of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol 2023; 81: 1076– 1126. 36697326
- [2]Tanskanen M, Peuralinna T, Polvikoski T, Notkola I-L, Sulkava R, Hardy J, Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study. Ann Med 2008; 40: 232– 239. 18382889
- [3]Scully PR, Treibel TA, Fontana M, Lloyd G, Mullen M, Pugliese F, Prevalence of Cardiac Amyloidosis in Patients Referred for Transcatheter Aortic Valve Replacement. J Am Coll Cardiol 2018; 71: 463– 464. 29389364 PMC5780297
- [4]Castaño A, Narotsky DL, Hamid N, Khalique OK, Morgenstern R, DeLuca A, Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement. Eur Heart J 2017; 38: 2879– 2887. 29019612 PMC5837725
- [5]AbouEzzeddine OF, Davies DR, Scott CG, Fayyaz AU, Askew JW, McKie PM, Prevalence of Transthyretin Amyloid Cardiomyopathy in Heart Failure With Preserved Ejection Fraction. JAMA Cardiol 2021; 6: 1267– 1274. 34431962 PMC8387947
- [6]González-López E, Gallego-Delgado M, Guzzo-Merello G, Haro-Del Moral FJ de, Cobo-Marcos M, Robles C, Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. Eur Heart J 2015; 36: 2585– 2594. 26224076
- [7]Maurer MS, Schwartz JH, Gundapaneni B, Elliott PM, Merlini G, Waddington-Cruz M, Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy. N Engl J Med 2018; 379: 1007– 1016. 30145929
- [8]Gillmore JD, Judge DP, Cappelli F, Fontana M, Garcia-Pavia P, Gibbs S, Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy. N Engl J Med 2024; 390: 132– 142. 38197816
- [9]Fontana M, Berk JL, Gillmore JD, Witteles RM, Grogan M, Drachman B, Vutrisiran in patients with transthyretin amyloidosis with cardiomyopathy. N Engl J Med 2025; 392: 33– 44. 39213194
- [10]Maurer MS, Kale P, Fontana M, Berk JL, Grogan M, Gustafsson F, Patisiran Treatment in Patients with Transthyretin Cardiac Amyloidosis. N Engl J Med 2023; 389: 1553– 1565. 37888916 PMC10757426
- [11]Benson Merrill D., Waddington-Cruz Márcia, Berk John L., Polydefkis Michael, Dyck Peter J., Wang Annabel K., Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis. N Engl J Med 2018; 379: 22– 31. 29972757 PMC12611561
- [12]Pablo Garcia-Pavia, aus dem Siepen Fabian, Donal Erwan, Lairez Olivier, van der Meer Peter, Kristen Arnt V., Phase 1 Trial of Antibody NI006 for Depletion of Cardiac Transthyretin Amyloid. N Engl J Med 2023; 389: 239– 250. 37212440
- [13]Ioannou A, Patel RK, Razvi Y, Porcari A, Sinagra G, Venneri L, Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years. Circulation 2022; 146: 1657– 1670. 36325894 PMC9698091
- [14]Spielvogel CP, Haberl D, Mascherbauer K, Ning J, Kluge K, Traub-Weidinger T, Diagnosis and prognosis of abnormal cardiac scintigraphy uptake suggestive of cardiac amyloidosis using artificial intelligence: a retrospective, international, multicentre, cross-tracer development and validation study. Lancet Digit Health 2024; 6: e251– e260. 38519153
- [15]Sangha V, Oikonomou EK, Khera R. Artificial Intelligence Applied to Electrocardiographic Images for Scalable Screening of Transthyretin Amyloid Cardiomyopathy. medRxiv. 2024. p. 2024.09.30.24314651.
- [16]Oikonomou EK, Vaid A, Holste G, Coppi A, McNamara RL, Baloescu C, Artificial intelligence-guided detection of under-recognised cardiomyopathies on point-of-care cardiac ultrasonography: a multicentre study. Lancet Digit Health 2025; 7: e113– e123. 39890242 PMC12084816
- [17]Holste G, Oikonomou EK, Mortazavi BJ, Wang Z, Khera R. Efficient deep learning-based automated diagnosis from echocardiography with contrastive self-supervised learning. Commun Med (Lond) 2024; 4: 133. 38971887 PMC11227494
- [18]Holste G, Oikonomou EK, Mortazavi BJ, Coppi A, Faridi KF, Miller EJ, Severe aortic stenosis detection by deep learning applied to echocardiography. Eur Heart J 2023; 44: 4592– 4604. 37611002 PMC11004929
- [19]Dorbala S, Ando Y, Bokhari S, Dispenzieri A, Falk RH, Ferrari VA, ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI Expert Consensus Recommendations for Multimodality Imaging in Cardiac Amyloidosis: Part 1 of 2-Evidence Base and Standardized Methods of Imaging. Circ Cardiovasc Imaging 2021; 14: e000029. 34196223
- [20]Ladefoged B, Dybro A, Povlsen JA, Vase H, Clemmensen TS, Poulsen SH. Diagnostic delay in wild type transthyretin cardiac amyloidosis - A clinical challenge. Int J Cardiol 2020; 304: 138– 143. 32033783
- [21]Oikonomou EK, Holste G, Yuan N, Coppi A, McNamara RL, Haynes NA, A multimodal video-based AI biomarker for aortic stenosis development and progression. JAMA Cardiol 2024; 9: 534– 544. 38581644 PMC10999005
- [23]Sangha V, Khunte A, Holste G, Mortazavi BJ, Wang Z, Oikonomou EK, Biometric contrastive learning for data-efficient deep learning from electrocardiographic images. J Am Med Inform Assoc 2024; 31: 855– 865. 38269618 PMC10990541
- [24]Sangha V, Mortazavi BJ, Haimovich AD, Ribeiro AH, Brandt CA, Jacoby DL, Automated multilabel diagnosis on electrocardiographic images and signals. Nat Commun 2022; 13: 1583. 35332137 PMC8948243
- [25]Coelho T, Dispenzieri A, Grogan M, Conceição I, Waddington-Cruz M, Kristen AV, Patients with transthyretin amyloidosis enrolled in THAOS between 2018 and 2021 continue to experience substantial diagnostic delay. Amyloid 2023; 30: 445– 448. 37459334
- [26]Ioannou A, Cappelli F, Emdin M, Nitsche C, Longhi S, Masri A, Stratifying Disease Progression in Patients With Cardiac ATTR Amyloidosis. J Am Coll Cardiol 2024; 83: 1276– 1291. 38530684 PMC11004588
- [27]Rauf MU, Hawkins PN, Cappelli F, Perfetto F, Zampieri M, Argiro A, Tc-99m labelled bone scintigraphy in suspected cardiac amyloidosis. Eur Heart J 2023; 44: 2187– 2198. 36946431 PMC10290871
- [28]Bokhari S, Castaño A, Pozniakoff T, Deslisle S, Latif F, Maurer MS. 99mTc-Pyrophosphate Scintigraphy for Differentiating Light-Chain Cardiac Amyloidosis From the Transthyretin-Related Familial and Senile Cardiac Amyloidoses. Circ Cardiovasc Imaging 2013; 6: 195– 201. 23400849 PMC3727049
- [29]Duffy G, Cheng PP, Yuan N, He B, Kwan AC, Shun-Shin MJ, High-Throughput Precision Phenotyping of Left Ventricular Hypertrophy With Cardiovascular Deep Learning. JAMA Cardiol 2022; 7: 386– 395. 35195663 PMC9008505
- [30]Goto S, Mahara K, Beussink-Nelson L, Ikura H, Katsumata Y, Endo J, Artificial intelligence-enabled fully automated detection of cardiac amyloidosis using electrocardiograms and echocardiograms. Nat Commun 2021; 12: 2726. 33976142 PMC8113484
- [31]Grogan M, Lopez-Jimenez F, Cohen-Shelly M, Dispenzieri A, Attia ZI, Abou Ezzedine OF, Artificial Intelligence-Enhanced Electrocardiogram for the Early Detection of Cardiac Amyloidosis. Mayo Clin Proc 2021; 96: 2768– 2778. 34218880
- [32]Witteles RM, Bokhari S, Damy T, Elliott PM, Falk RH, Fine NM, Screening for transthyretin amyloid cardiomyopathy in everyday practice. JACC Heart Fail 2019; 7: 709– 716. 31302046
- [33]Damrauer SM, Chaudhary K, Cho JH, Liang LW, Argulian E, Chan L, Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry. JAMA 2019; 322: 2191– 2202. 31821430 PMC7081752
- [34]Selvaraj S, Claggett BL, Quarta CC, Yu B, Inciardi RM, Buxbaum JN, Age Dependency of Cardiovascular Outcomes With the Amyloidogenic pV142I Transthyretin Variant Among Black Individuals in the US. JAMA Cardiol 2023; 8: 784– 788. 37212191 PMC10203968
- [35]Selvaraj S, Claggett B, Shah SH, Mentz RJ, Khouri MG, Manichaikul AW, Cardiovascular Burden of the V142I Transthyretin Variant. JAMA 2024; 331: 1824– 1833. 38734952 PMC11089467
- [36]Kittleson MM, Maurer MS, Ambardekar AV, Bullock-Palmer RP, Chang PP, Eisen HJ, Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association. Circulation 2020; 142: e7– e22. 32476490
- [37]Soman P, Garcia-Pavia P, Gillmore JD, Adams D, Conceicao I, Coelho T, Rationale & design of ACT-EARLY, the acoramidis transthyretin amyloidosis prevention trial: Early detection using cardiac radionuclide imaging. J Nucl Cardiol 2024; 38: 101948.
- [38]Spencer-Bonilla G, Njoroge JN, Pearson K, Witteles RM, Aras MA, Alexander KM. Racial and ethnic disparities in transthyretin cardiac amyloidosis. Curr Cardiovasc Risk Rep 2021; 15. PMC8916707 35280930
- [39]Oikonomou EK, Khera R. Artificial intelligence-enhanced patient evaluation: bridging art and science. Eur Heart J 2024; 45: 3204– 3218. 38976371 PMC11400875
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Dhingra, L. S., Aminorroaya, A., Sangha, V., Pedroso, A. F., Shankar, S. V., Coppi, A., Foppa, M., Brant, L. C. C., Barreto, S. M., Ribeiro, A. L. P., et al. (2025) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2025.01.030 · Cited by 53 · see citing works
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- Authors
- Oikonomou, E. K., Sangha, V., Vasisht Shankar, S., Coppi, A., Krumholz, H. M., Nasir, K., Miller, E. J., Gallegos-Kattan, C., Al-Mallah, M. H., Al-Kindi, S., & Khera, R.
- Affiliations
- Yale University (US)
- Yale New Haven Hospital (US)
- Houston Methodist (US)
- Corresponding author
- Khera, Rohan
- ORCID
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- medRxiv
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- openRxiv
- Published
- 2024-08-26
- PMC
- PMC11383475
- OpenAlex
- W4401881914
- Cited by
- 7
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- 1
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- 2025: 6 · 2024: 1
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- doi.org
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- medRxiv (acceptedVersion, cc-by-nd)
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- Funders
- National Institutes of Health (1r01ag089981-01)
- National Heart, Lung, and Blood Institute (F32HL170592, R01HL167858, K23HL153775)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Amyloidosis: Diagnosis, Treatment, Outcomes
- Health Sciences › Medicine › Health Informatics › Artificial Intelligence in Healthcare and Education
- Health Sciences › Health Professions › Health Information Management › Artificial Intelligence in Healthcare
- Keywords
- transthyretin amyloid cardiomyopathy, electrocardiogram, deep learning, transthoracic echocardiography, longitudinal disease monitoring, cardiac imaging biomarkers
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