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Acute Myocarditis Associated With Desmosomal Gene Variants.

Authors :
Ammirati E
Raimondi F
Piriou N
Sardo Infirri L
Mohiddin SA
Mazzanti A
Shenoy C
Cavallari UA
Imazio M
Aquaro GD
Olivotto I
Pedrotti P
Sekhri N
Van de Heyning CM
Broeckx G
Peretto G
Guttmann O
Dellegrottaglie S
Scatteia A
Gentile P
Merlo M
Goldberg RI
Reyentovich A
Sciamanna C
Klaassen S
Poller W
Trankle CR
Abbate A
Keren A
Horowitz-Cederboim S
Cadrin-Tourigny J
Tadros R
Annoni GA
Bonoldi E
Toquet C
Marteau L
Probst V
Trochu JN
Kissopoulou A
Grosu A
Kukavica D
Trancuccio A
Gil C
Tini G
Pedrazzini M
Torchio M
Sinagra G
Gimeno JR
Bernasconi D
Valsecchi MG
Klingel K
Adler ED
Camici PG
Cooper LT Jr
Source :
JACC. Heart failure [JACC Heart Fail] 2022 Oct; Vol. 10 (10), pp. 714-727. Date of Electronic Publication: 2022 Sep 07.
Publication Year :
2022

Abstract

Background: The risk of adverse cardiovascular events in patients with acute myocarditis (AM) and desmosomal gene variants (DGV) remains unknown.<br />Objectives: The purpose of this study was to ascertain the risk of death, ventricular arrhythmias, recurrent myocarditis, and heart failure (main endpoint) in patients with AM and pathogenic or likely pathogenetic DGV.<br />Methods: In a retrospective international study from 23 hospitals, 97 patients were included: 36 with AM and DGV (DGV[+]), 25 with AM and negative gene testing (DGV[-]), and 36 with AM without genetics testing. All patients had troponin elevation plus findings consistent with AM on histology or at cardiac magnetic resonance (CMR). In 86 patients, CMR changes in function and structure were re-assessed at follow-up.<br />Results: In the DGV(+) AM group (88.9% DSP variants), median age was 24 years, 91.7% presented with chest pain, and median left ventricular ejection fraction (LVEF) was 56% on CMR (P = NS vs the other 2 groups). Kaplan-Meier curves demonstrated a higher risk of the main endpoint in DGV(+) AM compared with DGV(-) and without genetics testing patients (62.3% vs 17.5% vs 5.3% at 5 years, respectively; P < 0.0001), driven by myocarditis recurrence and ventricular arrhythmias. At follow-up CMR, a higher number of late gadolinium enhanced segments was found in DGV(+) AM.<br />Conclusions: Patients with AM and evidence of DGV have a higher incidence of adverse cardiovascular events compared with patients with AM without DGV. Further prospective studies are needed to ascertain if genetic testing might improve risk stratification of patients with AM who are considered at low risk.<br />Competing Interests: Funding Support and Author Disclosures Dr Ammirati has received a grant from the Italian Ministry of Health (GR-2019-12368506) and is a consultant for Kiniksa and Cytokinetics. Dr Adler is a consultant for Abbott, Abiomed, AstraZeneca, Endotronix, Ionis, Medtronic, and Novartis; is on the board of directors of Genstem Therapeutics; and is a shareholder of Rocket Pharmaceuticals. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.<br /> (Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2213-1787
Volume :
10
Issue :
10
Database :
MEDLINE
Journal :
JACC. Heart failure
Publication Type :
Academic Journal
Accession number :
36175056
Full Text :
https://doi.org/10.1016/j.jchf.2022.06.013