Evidence map›Paper›PMID 41884351›Full record

ArticleMachine learning. Health2026

Machine learning models enhance detection of arrhythmogenic right ventricular cardiomyopathy.

Kwaku K Quansah, Sean A Murphy, Esther Kwon, Emma Anderson, Crystal Tichnell, Brittney Murray, Sean Gaines, Alessio Gasperetti, Cynthia A James, Hugh Calkins and 2 more

Abstract read
In one paragraph

Article in Machine learning. Health, 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
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Kwaku K QuansahDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.ORCID https://orcid.org/0000-0002-2981-5874
Sean A MurphyDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Esther KwonDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Emma AndersonDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Crystal TichnellDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Brittney MurrayDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Sean GainesDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Alessio GasperettiDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Cynthia A JamesDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Hugh CalkinsDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Richard T CarrickDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.
Chulan KwonDepartment of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21202, United States of America.

Funding

Microphysiological Model of Human Cardiac Sympathetic InnervationR01HL164936 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KIM, DEOK-HO, KWON, CHULAN · 2022 to 2025
$3.2M
Targeting Dysregulated Maturation Program in PSC-CardiomyocytesR01HL171205 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Chulan Kwon · 2024 to 2026
$2.2M
American Heart Association-American Stroke Association 23IPA1051956NHLBI NIH HHS R01 HL164936NHLBI NIH HHS R01 HL171205
6 · The paper itself

Abstract

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable cardiac disorder associated with sudden cardiac death, yet its diagnosis remains slow, resource-intensive, and dependent on expert interpretation of multimodal tests. Machine learning approaches may enable earlier and more standardized detection. Here, we sought to identify an optimal machine learning strategy for ARVC detection, and to define its role within the diagnostic pathway. A composite dataset of 688 patients from the Johns Hopkins ARVC Registry was used to train and evaluate eight models based on 31 clinical, electrocardiogram (ECG), imaging, and genetic variables. Following an 80/20 train-test split, models were developed on the train set using five-fold stratified cross-validation and evaluated on the hold-out test cohort. Performance was assessed using area under the curve (AUC), accuracy, sensitivity, specificity, and 95% confidence intervals. Model comparison was performed using the Friedman test with Nemenyi post-hoc analysis. Gradient boosted trees (GBT) achieved the highest overall performance (AUC = 0.943, 95% CI: 0.902-0.99; accuracy = 0.847, 95% CI: 0.786-0.907). Nemenyi testing showed GBT significantly outperformed Decision Tree and TabNet (

Indexed as

arrhythmogenic right ventricular cardiomyopathyclinical decision-makingdiagnostic supportgradient boosted treesmachine learningmatrix clinical datapredictive modeling

Identifiers

PMID41884351
PMCPMC13012209

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.