Evidence map›Paper›PMID 40832996›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2025

Different underlying aetiologies in patients presenting with ventricular tachycardia fulfilling task force criteria for arrhythmogenic right ventricular cardiomyopathy: initial suspicion based on the 12-lead electrocardiogram.

Jarieke C Hoogendoorn, Laurens P Bosman, Jeroen F van der Heijden, Arthur A Wilde, Maarten P van den Berg, Sing-Chien Yap, J Peter van Tintelen, Dennis Dooijes, Anneline S J M Te Riele, Katja Zeppenfeld

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Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jarieke C HoogendoornDepartment of Cardiology, Willem Einthoven Center for Cardiac Arrhythmia Research and Management (WECAM), Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-8090-2447
Laurens P BosmanDepartment of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.ORCID 0000-0001-5037-1158
Jeroen F van der HeijdenDepartment of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.
Arthur A WildeDepartment of Cardiology, Heart Centre, Amsterdam UMC Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.ORCID 0000-0002-0528-0852
Maarten P van den BergDepartment of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0000-0002-1493-2998
Sing-Chien YapEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart ).ORCID 0000-0003-4520-2725
J Peter van TintelenDepartment of Genetics, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-3854-6749
Dennis DooijesDepartment of Genetics, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-0312-5354
Anneline S J M Te RieleDepartment of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.ORCID 0000-0002-4694-4790
Katja ZeppenfeldDepartment of Cardiology, Willem Einthoven Center for Cardiac Arrhythmia Research and Management (WECAM), Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-7034-1017

Funding

Biosense WebsterBiotronikBoston ScientificEdwards LifesciencesHorizon IMPACT #101115536MedtronicZonMw
6 · The paper itself

Abstract

aimsThe task force criteria (TFC) for arrhythmogenic right ventricular cardiomyopathy (ARVC) are highly sensitive but lack specificity. Atypical RV involvement (aRVi) may indicate different underlying aetiologies and prognosis, requiring specific therapeutic interventions. We aimed to evaluate the role of the baseline 12-lead ECG for initial suspicion of aRVi.

methodsFrom the Netherlands Heart Institute Arrhythmogenic Cardiomyopathy (NHI-ACM) registry, patients were selected who (i) fulfilled TFC for definite ARVC, (ii) presented with sustained ventricular tachycardia (VT), and (iii) underwent genetic testing. The first available ECG after VT was evaluated. PR prolongation ≥220 ms and/or a surface area of the maximum R'-wave in V1-V3 of ≥1.65 mm2 was defined as an aRVi-ECG. Patients with an ARVC-related pathogenic/likely pathogenic variant (P/LP+) were classified as 'ARVC'. Data of P/LP- were reviewed by an expert panel and classified as either 'ARVC' or 'different aetiology' based on consensus.

resultsA total of 159 patients were included (122 P/LP+ and 37 P/LP- patients). Nineteen patients had an aRVi-ECG [11 (9%) P/LP+ vs. 8 (22%) P/LP-, P = 0.038]. Of the P/LP- patients, 17 (46%) were classified as 'different aetiology' (e.g. myocarditis, ischaemia, sarcoidosis), including all 8 patients with an aRVi-ECG. Among the P/LP+ patients with an aRVi-ECG, 46% carried the p.Arg14del phospholamban pathogenic variant, and 64% died compared to 15 and 19% of P/LP+ patients without an aRVi-ECG, respectively (both P < 0.01).

conclusionIn P/LP- patients presenting with VT and fulfilling TFC, an aRVi-ECG should raise suspicion for a different underlying aetiology. In P/LP+ patients, an aRVi-ECG may identify those with poor outcome.

Indexed as

Arrhythmogenic Right Ventricular DysplasiaElectrocardiographyTachycardia, VentricularAction PotentialsAdultFemaleGenetic TestingHeart RateHumansMaleMiddle AgedNetherlandsPredictive Value of TestsRegistriesArrhythmogenic right ventricular cardiomyopathyCardiac sarcoidosisElectrocardiogramVentricular tachycardia

Identifiers

PMID40832996
PMCPMC12365759

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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.