DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort

Author:

Di Lorenzo Francesca1ORCID,Marchionni Enrica2ORCID,Ferradini Valentina1,Latini Andrea1,Pezzoli Laura3ORCID,Martino Annamaria4,Romeo Fabiana4ORCID,Iorio Annamaria5,Bianchi Stefano6,Iascone Maria3ORCID,Calò Leonardo4,Novelli Giuseppe1ORCID,Mango Ruggiero7,Sangiuolo Federica1ORCID

Affiliation:

1. Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy

2. Medical Genetics, Policlinico Tor Vergata, 00133 Rome, Italy

3. Laboratory of Medical Genetics, ASST Papa Giovanni XXIII, 24127 Bergamo, Italy

4. Department of Cardiology, Policlinico Casilino, 00169 Rome, Italy

5. Cardiology Department, ASST Papa Giovanni XXIII Bergamo, 24127 Bergamo, Italy

6. UOC Cardiologia, Ospedale Fatebenefratelli Isola Tiberina, 00186 Rome, Italy

7. House of Care D4, Local Health Authority Roma 2, 00185 Rome, Italy

Abstract

Variants in desmoplakin gene (DSP MIM *125647) have been usually associated with Arrhythmogenic Cardiomyopathy (ACM), or Dilated Cardiomyopathy (DCM) inherited in an autosomal dominant manner. A cohort of 18 probands, characterized as heterozygotes for DSP variants by a target Next Generation Sequencing (NGS) cardiomyopathy panel, was analyzed. Cardiological, genetic data, and imaging features were retrospectively collected. A total of 16 DSP heterozygous pathogenic or likely pathogenic variants were identified, 75% (n = 12) truncating variants, n = 2 missense variants, n = 1 splicing variant, and n = 1 duplication variant. The mean age at diagnosis was 40.61 years (IQR 31–47.25), 61% of patients being asymptomatic (n = 11, New York Heart Association (NYHA) class I) and 39% mildly symptomatic (n = 7, NYHA class II). Notably, 39% of patients (n = 7) presented with a clinical history of presumed myocarditis episodes, characterized by chest pain, myocardial enzyme release, 12-lead electrocardiogram abnormalities with normal coronary arteries, which were recurrent in 57% of cases (n = 4). About half of the patients (55%, n = 10) presented with a varied degree of left ventricular enlargement (LVE), four showing biventricular involvement. Eleven patients (61%) underwent implantable cardioverter defibrillator (ICD) implantation, with a mean age of 46.81 years (IQR 36.00–64.00). Cardiac magnetic resonance imaging (CMRI) identified in all 18 patients a delayed enhancement (DE) area consistent with left ventricular (LV) myocardial fibrosis, with a larger localization and extent in patients presenting with recurrent episodes of myocardial injury. These clinical and genetic data confirm that DSP-related cardiomyopathy may represent a distinct clinical entity characterized by a high arrhythmic burden, variable degrees of LVE, Late Gadolinium Enhancement (LGE) with subepicardial distribution and episodes of myocarditis-like picture.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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