Evidence map›Paper›PMID 42200278›Full record

ArticleCirculation. Cardiovascular imaging2026

Multimodal Artificial Intelligence for Cardiac Amyloidosis Diagnosis: Integrating Echocardiography With Clinical and Laboratory Data for Improved Detection.

Jeremy A Slivnick, Sze Chi Lim, Michael Randazzo, Mathew S Maurer, Stephen Helmke, Marielle Scherrer-Crosbie, Azin Vakilpour, Karolina M Zareba, Akash Goyal, Richard Cheng and 20 more

Abstract read
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Article in Circulation. Cardiovascular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Jeremy A SlivnickUniversity of Chicago, IL (J.A.S., N.S., K.A., R.M.L.).ORCID 0000-0002-2327-4544
Sze Chi LimUs2.AI, Singapore (S.C.L., M. Frost, C.L.S.P.).ORCID 0000-0001-8153-858X
Michael RandazzoHospital of the University of Pennsylvania, Philadelphia (M.R., M.S.-C., A.V.).
Mathew S MaurerHospital of the University of Pennsylvania, Philadelphia (M.R., M.S.-C., A.V.).ORCID 0000-0001-5400-5008
Stephen HelmkeColumbia University Irving Medical Center, New York (M.S.M., S.H.).ORCID 0000-0003-2764-3009
Marielle Scherrer-CrosbieHospital of the University of Pennsylvania, Philadelphia (M.R., M.S.-C., A.V.).ORCID 0000-0001-6375-9266
Azin VakilpourHospital of the University of Pennsylvania, Philadelphia (M.R., M.S.-C., A.V.).
Karolina M ZarebaThe Ohio State University Wexner Medical Center, Columbus (K.M.Z., A.G.).ORCID 0000-0002-4891-4106
Akash GoyalThe Ohio State University Wexner Medical Center, Columbus (K.M.Z., A.G.).ORCID 0000-0002-9293-3523
Richard ChengUniversity of Washington, Seattle (R.C., N.N.).
Nicole NakamatsuUniversity of Washington, Seattle (R.C., N.N.).ORCID 0009-0005-9567-3551
Tetsuji KitanoHospital of University of Occupational and Environmental Health, Japan (T.K., M.T.).ORCID 0000-0002-8539-5907
Masaaki TakeuchiHospital of University of Occupational and Environmental Health, Japan (T.K., M.T.).ORCID 0000-0001-7606-1537
Viviane Tiemi HottaHeart Institute (InCor), Sao Paolo, Brazil (V.T.H., M.L.C.V.).ORCID 0000-0002-9236-3815
Marcelo Luiz Campos VieiraHeart Institute (InCor), Sao Paolo, Brazil (V.T.H., M.L.C.V.).ORCID 0000-0002-4561-5717
Pablo ElissamburuICBA, Buenos Aires, Argentina (P.E., R.E.R.).ORCID 0009-0008-5760-9227
Ricardo E RonderosICBA, Buenos Aires, Argentina (P.E., R.E.R.).
Aldo PradoCentro Privado de Cardiología, Tucuman, Argentina (A. Prado).ORCID 0000-0002-6057-700X
Efstratios KoutroumpakisUniversity of Texas MD Anderson Cancer Center, Houston (E.K., A.D.).ORCID 0000-0002-6757-6480
Anita DeswalUniversity of Texas MD Anderson Cancer Center, Houston (E.K., A.D.).ORCID 0000-0002-6147-9591
Amit PursnaniEndeavor NorthShore, Evanston, IL (A. Pursnani).ORCID 0000-0001-5616-8839
Nitasha SarswatUniversity of Chicago, IL (J.A.S., N.S., K.A., R.M.L.).ORCID 0000-0003-0233-7881
Karima AddetiaUniversity of Chicago, IL (J.A.S., N.S., K.A., R.M.L.).
Juan CotellaAltos de Salta Swiss Medical Group, Tucuman, Argentina (J.C.).ORCID 0000-0003-4317-8725
Frederick L RubergBoston University Chobanian and Avedisian School of Medicine, MA (F.L.R.).ORCID 0000-0002-6424-4413
Matthew FrostUs2.AI, Singapore (S.C.L., M. Frost, C.L.S.P.).ORCID 0009-0006-9760-4784
Marianna FontanaNational Amyloidosis Center, London, United Kingdom (M. Fontana).ORCID 0000-0002-9233-9831
Carolyn Lam Su PingUs2.AI, Singapore (S.C.L., M. Frost, C.L.S.P.).ORCID 0000-0003-1903-0018
Roberto M LangUniversity of Chicago, IL (J.A.S., N.S., K.A., R.M.L.).
Federico M AschMedStar Health Research Institute, Washington, DC (F.M.A.).ORCID 0000-0002-1744-5271

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiac 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.

methodsWe 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.

resultsIn 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%;

conclusionsA 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.

Indexed as

AmyloidosisArtificial IntelligenceCardiomyopathiesEchocardiographyImmunoglobulin Light-chain AmyloidosisAgedAmyloid Neuropathies, FamilialBiomarkersFemaleHumansIntelligent SystemsMaleMiddle AgedPredictive Value of TestsRegistriesReproducibility of ResultsBiomarkersamyloidosisartificial intelligencebiomarkersdeep learningheart failureprealbumin

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.