RT Journal Article
SR Electronic
T1 Coexistence of cardiac sarcoidosis and arrhythmogenic cardiomyopathy-associated genetic variants: a multicentre case-control study
JF Heart
JO Heart
FD BMJ Publishing Group Ltd and British Cardiovascular Society
SP 480
OP 486
DO 10.1136/heartjnl-2024-324525
VO 111
IS 10
A1 Rossi, Valentina Alice
A1 Palazzini, Matteo
A1 Ammirati, Enrico
A1 Gasperetti, Alessio
A1 Grubler, Martin
A1 Brunckhorst, Corinna
A1 Manka, Robert
A1 Giannopoulos, Andreas
A1 Tanner, Felix C
A1 Medeiros-Domingo, Argelia
A1 Gentile, Piero
A1 Bramerio, Manuela
A1 Schmidt, Dörthe
A1 Tondo, Claudio
A1 Flammer, Andreas J
A1 Ruschitzka, Frank
A1 Duru, Firat
A1 Saguner, Ardan Muammer
YR 2025
UL http://heart.bmj.com/content/111/10/480.abstract
AB Background Cardiac sarcoidosis (CS) is a chronic inflammatory disease characterised by non-caseating granulomas, while arrhythmogenic cardiomyopathy (ACM) is a genetic condition mainly affecting desmosomal proteins. The coexistence of CS and genetic variants associated with ACM is not well understood, creating challenges in diagnosis and management. This study aimed to describe the clinical, imaging and genetic features of patients with both conditions.Methods This was a multicentre retrospective case-control study involving three groups of patients: those with biopsy-proven CS and pathogenic or likely pathogenic genetic variants linked to ACM (n=5); patients with genetic variants but no CS (n=5); and patients with CS without genetic variants (n=5). Clinical data, including symptoms, electrocardiographic findings and imaging results from echocardiography, cardiac magnetic resonance and positron-emission tomography, were analysed.Results Patients with CS and genetic variants were more likely to exhibit atrioventricular block (100%), PR prolongation (204 ms vs 160 ms) and paroxysmal atrial fibrillation (80%) compared with those with genetic variants alone (0% for both). Imaging findings showed a higher prevalence of septal involvement in patients with both conditions (80%) than in those with genetic variants alone (20%). No significant differences were observed between patients with CS and genetic variants and those with CS without genetic variants. The genetic variants identified included variants in PKP2 (40%), DSG2 (20%), DSP (20%) and TTN (20%).Conclusions The coexistence of CS and ACM-associated genetic variants is associated with distinct clinical features, including PR prolongation, AVB1°, septal involvement and paroxysmal atrial fibrillation. These findings emphasise the need to evaluate for CS in individuals with ACM and associated genetic variants who present with conduction abnormalities or septal involvement, guiding tailored diagnostic and therapeutic strategies.Data are available upon reasonable request.