Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers

J Am Coll Cardiol. 2013 Nov 5;62(19):1761-9. doi: 10.1016/j.jacc.2012.11.087. Epub 2013 Jun 27.

Abstract

Objectives: The aim of this study was to identify the incremental value and optimal role of cardiac magnetic resonance (CMR) imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C)-associated desmosomal mutation carriers without histories of sustained ventricular arrhythmia.

Background: Risk stratification of ARVD/C mutation carriers is challenging.

Methods: Sixty-nine patients (mean age 27.0 ± 15.3 years, 42% men) harboring ARVD/C-associated pathogenic mutations (83% plakophilin 2) without prior sustained ventricular arrhythmias were included. Electrocardiographic and 24-h Holter monitoring findings closest to presentation were analyzed for electrical abnormalities per revised task force criteria. CMR studies were done to identify abnormal cardiac structure and function according to the revised task force criteria.

Results: Overall, 42 patients (61%) presented with electrical abnormalities on the basis of electrocardiography and Holter monitoring, of whom 20 (48%) had abnormal results on CMR. Only 1 of 27 patients (4%) without electrical abnormalities at initial evaluation had abnormal CMR results. Over a mean follow-up period of 5.8 ± 4.4 years, 11 patients (16%) experienced sustained ventricular arrhythmias, exclusively in patients with both electrical abnormalities (electrocardiography and/or Holter monitoring) and abnormal CMR results.

Conclusions: These results suggest that electrical abnormalities on electrocardiography and Holter monitoring precede detectable structural abnormalities in ARVD/C mutation carriers. Therefore, evaluation of cardiac structure and function using CMR is probably not necessary in the absence of baseline electrical abnormalities. Among ARVD/C mutation carriers, the presence of both electrical and CMR abnormalities identifies patients at high risk for events and thus patients who might benefit from prophylactic implantable cardioverter-defibrillator placement.

Keywords: ARVD/C; CI; CMR; ECG; ICD; RV; TFC; VT; arrhythmogenic right ventricular dysplasia/cardiomyopathy; cardiac magnetic resonance; cardiomyopathy; confidence interval; electrocardiographic; electrocardiography; implantable cardioverter-defibrillator; magnetic resonance imaging; right ventricular; risk stratification; tachyarrhythmias; task force criteria; ventricular tachycardia.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arrhythmogenic Right Ventricular Dysplasia / diagnosis*
  • Arrhythmogenic Right Ventricular Dysplasia / epidemiology
  • Arrhythmogenic Right Ventricular Dysplasia / genetics
  • DNA / genetics
  • DNA Mutational Analysis
  • Desmosomes / genetics*
  • Electrocardiography, Ambulatory
  • Female
  • Follow-Up Studies
  • Genetic Predisposition to Disease*
  • Heterozygote
  • Humans
  • Incidence
  • Magnetic Resonance Imaging, Cine / methods*
  • Male
  • Maryland / epidemiology
  • Mutation*
  • Plakophilins / genetics
  • Retrospective Studies
  • Risk Assessment / methods*
  • Young Adult

Substances

  • Plakophilins
  • DNA