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DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort.
Di Lorenzo, Francesca; Marchionni, Enrica; Ferradini, Valentina; Latini, Andrea; Pezzoli, Laura; Martino, Annamaria; Romeo, Fabiana; Iorio, Annamaria; Bianchi, Stefano; Iascone, Maria; Calò, Leonardo; Novelli, Giuseppe; Mango, Ruggiero; Sangiuolo, Federica.
Afiliación
  • Di Lorenzo F; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Marchionni E; Medical Genetics, Policlinico Tor Vergata, 00133 Rome, Italy.
  • Ferradini V; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Latini A; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Pezzoli L; Laboratory of Medical Genetics, ASST Papa Giovanni XXIII, 24127 Bergamo, Italy.
  • Martino A; Department of Cardiology, Policlinico Casilino, 00169 Rome, Italy.
  • Romeo F; Department of Cardiology, Policlinico Casilino, 00169 Rome, Italy.
  • Iorio A; Cardiology Department, ASST Papa Giovanni XXIII Bergamo, 24127 Bergamo, Italy.
  • Bianchi S; UOC Cardiologia, Ospedale Fatebenefratelli Isola Tiberina, 00186 Rome, Italy.
  • Iascone M; Laboratory of Medical Genetics, ASST Papa Giovanni XXIII, 24127 Bergamo, Italy.
  • Calò L; Department of Cardiology, Policlinico Casilino, 00169 Rome, Italy.
  • Novelli G; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Mango R; House of Care D4, Local Health Authority Roma 2, 00185 Rome, Italy.
  • Sangiuolo F; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
Int J Mol Sci ; 24(3)2023 Jan 27.
Article en En | MEDLINE | ID: mdl-36768812
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cardiomiopatías / Miocarditis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cardiomiopatías / Miocarditis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article