Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/47479
Title: Paddling through palpitations: when genes, myocardial inflammation and exercise collide-a case report of arrhythmogenic cardiomyopathy in a young competitive rower
Authors: DELPIRE, Boris 
GHEKIERE, Olivier 
Dilling-Boer, Dagmara
KOOPMAN, Pieter 
CLAESSEN, Guido 
Editors: Sommer, Philipp
Duncker, David
Sohns, Christian
Ranganathan, Deepti
Issue Date: 2025
Publisher: OXFORD UNIV PRESS
Source: European heart journal. Case reports, 9 (9) (Art N° ytaf442)
Abstract: Background Arrhythmogenic cardiomyopathy (ACM) is characterized by fibrofatty replacement of myocardium, predisposing to ventricular arrhythmias and sudden cardiac death. Arrhythmogenic cardiomyopathy is often linked to desmosomal gene mutations, particularly PKP2, which encodes plakophilin-2, a key structural protein in cardiac intercalated discs. In individuals with PKP2 mutations, exercise has been shown to accelerate disease progression.Case summary A 22-year-old male semi-professional rower presented with palpitations, pre-syncope, and a history of presumed myocarditis with subepicardial fibrosis on cardiac magnetic resonance (CMR). Workup revealed anterior T-wave inversions on resting ECG and sustained monomorphic right ventricular (RV) outflow tract tachycardia, induced during exercise testing. Repeat CMR showed RV dysfunction and non-ischaemic RV and LV fibrosis with fibrofatty replacement. The patient met diagnostic criteria for biventricular ACM and underwent catheter ablation targeting the arrhythmic substrate. A multidisciplinary team carefully considered ICD therapy. However, due to the limited extent of the arrhythmic substrate, the exercise-induced nature of the ventricular tachycardia, and the successful ablation, ICD implantation was deferred at this stage. An ILR was implanted for continuous rhythm monitoring, with a low threshold for future ICD placement. High-intensity sports restriction, pharmacological therapy, and genetic counselling were initiated. Genetic testing identified a pathogenic PKP2 mutation.Discussion This case highlights the complex interplay of genetic predisposition, myocardial inflammation, and exercise in ACM expression. The presumed myocarditis likely represented a 'hot phase' of ACM, accelerating structural cardiac changes. High-intensity exercise then acted as a 'second hit,' triggering phenotypic expression. Multidisciplinary evaluation combining rhythm monitoring, imaging, and genetic testing was key to diagnosis and management.
Notes: Delpire, B (corresponding author), Jessa Hosp, Dept Cardiol, Hartctr, Stadsomvaart 11, B-3500 Hasselt, Belgium.; Delpire, B (corresponding author), UHasselt, LCRC, Fac Med & Life Sci, B-3590 Diepenbeek, Belgium.; Delpire, B (corresponding author), Katholieke Univ Leuven, Dept Cardiovasc Sci, Herestr 49, B-3000 Leuven, Belgium.; Delpire, B (corresponding author), UZ Leuven, Dept Cardiovasc Dis, Herestr 49, B-3000 Leuven, Belgium.
boris.delpire@uhasselt.be
Keywords: Sports cardiology;Ventricular arrhythmias;Arrhythmogenic cardiomyopathy;Myocarditis;PKP2;Case report
Document URI: http://hdl.handle.net/1942/47479
e-ISSN: 2514-2119
DOI: 10.1093/ehjcr/ytaf442
ISI #: 001576487800001
Rights: The Author(s) 2025. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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