Evidence map›Paper›PMID 42479339›Full record

ArticleThe international journal of cardiovascular imaging2026

Machine learning algorithms for predicting arrhythmic events in Hypertrophic Cardiomyopathy: limited enhancement beyond late gadolinium enhancement.

Joana Certo Pereira, Rita Amador, Armando Vieira, Rita Almeida Carvalho, Bruno Castilho, Edmundo Arteaga, Carlos Rochitte, Bruno Rocha, Pedro Lopes, João Abecasis and 3 more

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Article in The international journal of cardiovascular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

13 authors.

Joana Certo PereiraDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal. joanacerto@gmail.com.ORCID http://orcid.org/0000-0002-3632-4459
Rita AmadorDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
Armando VieiraMEDgicalAI Company, Lisbon, Portugal.
Rita Almeida CarvalhoDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
Bruno CastilhoMEDgicalAI Company, Lisbon, Portugal.
Edmundo ArteagaDepartment of Cardiology, Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brasil.
Carlos RochitteDepartment of Cardiology, Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brasil.
Bruno RochaDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
Pedro LopesDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
João AbecasisDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
Pedro FreitasDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
Pedro AdragãoDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.
António M FerreiraDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to develop and assess the performance of a Machine learning (ML) model integrating common clinical features to predict arrhythmic events in patients with Hypertrophic Cardiomyopathy (HCM). Post-hoc analysis of an international multicenter registry of 531 HCM patients (49 years (IQR 35-61), 57% male) who underwent cardiac magnetic resonance (CMR). The dataset comprised clinical, echocardiographic, and CMR variables, including quantification of late gadolinium enhancement (LGE) using the + 6 SD method. The endpoint was a composite of sudden cardiac death (SCD), aborted SCD, and sustained ventricular tachycardia (VT). A total of 28 events occurred over a median follow-up of 4.1 (IQR 1.8-7.3) years. Several ML models were developed and the predictive performance of the best model was compared to the ESC HCM risk score and to the amount of LGE. The Random Forest (RF) was the most effective method showing a good performance for predicting arrhythmic events [AUC of 0.78 (95% CI: 0.76-0.82, p < 0.001)], substantially outperforming the ESC HCM risk score [AUC of 0.64 (95% CI 0.62-0.67; p < 0.001), p < 0.001 for comparison]. However, when compared to LGE alone [AUC of 0.76 (95% CI: 0.73-0.84, p < 0.001)], the RF model did not provide significant improvement in predicting the endpoint (p = 0.817 for comparison). A ML model using available clinical variables significantly outperformed the ESC HCM risk score in predicting arrhythmic events in HCM. However, its incremental value over LGE alone was weak, underscoring the strong predictive value of this imaging marker. This findings should be interpreted as exploratory and hypothesis-generating.

Indexed as

Arrhythmic risk predictionHypertrophic cardiomyopathyLate gadolinium enhancementMachine learningRandom forestSudden cardiac death

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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.