Desmoplakin Cardiomyopathy: Role of Inflammation and Potential Role of Disease-Modifying Therapies

Alessio Gasperetti*, Richard T. Carrick, Steven Muller, Brittney Murray, Luigi Adamo, Barbara Bauce, Elizabeth McNally, Adam Helms

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Purpose of Review: To summarize the available data on the use of immunosuppression therapies for the management of hot phases of disease and recurrent myocarditis in patients with desmoplakin cardiomyopathy (DSP-CMP). Recent Findings: Occurrence of myocarditis episodes has been associated with worsening of outcomes in DSP-CMP. Multiple case reports and small case series have described potential benefit in using anti-inflammatory and immunosuppressive medications for the treatment of those episodes. Recently published translational data has shown a clear link between DSP variants and a propensity to inflammation. Summary: The presence of acute myocarditis episodes have been clearly demonstrated as a manifestation of DSP-CMP. These episodes are marked by myocardial inflammation and subsequent fibrosis, and, moreover, contribute to a heightened future risk of subsequent arrhythmias and heart failure. Identifying optimal strategies to prevent and/or interrupt myocardial inflammation is therefore a critical priority of patients with DSP-CMP.

Original languageEnglish
Article number12
Number of pages8
JournalCurrent cardiology reports
Volume27
Issue number1
DOIs
Publication statusPublished - 9 Jan 2025

Keywords

  • Arrhythmogenic cardiomyopathy
  • DSP
  • DSP-cardiomyopathy
  • Immunosuppression
  • Myocarditis

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