Evidence map›Paper›PMID 42667014›Full record

ArticleEuropean heart journal. Digital health2026

Subtype specific artificial intelligence modelling of cardiac amyloidosis using echocardiography and electrocardiography.

Jose K James, Surendra Dasari, Jennifer M Amadio, Christopher G Scott, Eli Muchtar, Morie A Gertz, Shaji Kumar, Francis K Buadi, David Dingli, Taxiarchis V Kourelis and 7 more

Abstract read
In one paragraph

Article in European heart journal. Digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Jose K JamesDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0003-0482-7307
Surendra DasariDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Jennifer M AmadioDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0002-6826-5596
Christopher G ScottDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Eli MuchtarDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0003-2210-2174
Morie A GertzDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0002-3853-5196
Shaji KumarDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0001-5392-9284
Francis K BuadiDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0003-3214-0203
David DingliDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0001-7477-3004
Taxiarchis V KourelisDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0001-8573-9434
Itzhak Z AttiaDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Francisco Lopez-JimenezDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0001-5788-9734
Omar AbouEzzeddineDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0003-3256-3660
Dennis H MurphreeDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0002-7800-455X
Paul A FriedmanDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0001-5052-2948
Martha GroganDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0002-2541-4440
Angela DispenzieriDepartment of Hematology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.ORCID https://orcid.org/0000-0001-8780-9512

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: We aimed to develop and validate echocardiography-based prediction models for light chain (AL) and transthyretin (ATTR) cardiac amyloidosis and to quantify the incremental value of integrating artificial intelligence-derived electrocardiography (ECG) probabilities. Methods and results: We conducted a retrospective, multisite study within a single health system including patients with AL or ATTR cardiac amyloidosis and matched control subjects. AL and ATTR cohorts were handled independently. For each subtype, patients were randomly split into training and test cohorts, with an additional temporally distinct test cohort. Logistic regression models were developed using structured echocardiographic variables with parsimonious core and extended feature sets, as well as models integrating these features with a previously validated AI ECG probability. Model performance was assessed using receiver operating characteristic and precision-recall (PR) analyses. In AL amyloidosis, echocardiography-based models demonstrated moderate discrimination in the primary test cohort (area under the PR curve, AUPRC 0.674) but were inferior to ECG alone (AUPRC 0.824, Conclusion: Subtype-specific echocardiography-based models demonstrate robust discrimination for cardiac amyloidosis, with divergent contributions of echocardiographic features by subtype. These results support tailored modelling strategies and prospective concurrent deployment of AL and ATTR models.

Indexed as

AmyloidosisArtificial intelligenceEchocardiography

Identifiers

PMID42667014
PMCPMC13524381

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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.