Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus

Heart Rhythm. 2016 Apr;13(4):905-12. doi: 10.1016/j.hrthm.2015.12.006. Epub 2015 Dec 8.

Abstract

Background: Familial idiopathic ventricular fibrillation (IVF) is a severe disease entity and is notoriously difficult to manage because there are no clinical risk indicators for premature cardiac arrest. Previously, we identified a link between familial IVF and a risk haplotype on chromosome 7q36 (involving the arrhythmia gene DPP6).

Objective: The purpose of this study was to expand our knowledge of familial IVF and to discuss its (extended) clinical characteristics.

Methods: We studied 601 family members and probands: 286 DPP6 risk-haplotype positive (haplotype-positive) and 315 DPP6 risk-haplotype negative (haplotype-negative) individuals. Clinical parameters, a combination of all-cause mortality and (aborted) cardiac arrest and differences between haplotype-positives and haplotype-negatives, were evaluated.

Results: There were no differences in electrocardiographic indices between haplotype-positives and haplotype-negatives, or between haplotype-positives with or without events. Cardiac magnetic resonance documented slightly larger ventricular volumes in haplotype-positives compared to controls (P <.05), but these were not clinically useful. Mortality and/or cardiac arrest occurred in 85 haplotype-positives (30%) and 18 haplotype-negatives (6%). Twenty-four haplotype-positives (8% male) were resuscitated from ventricular fibrillation (VF). Documented VF was always elicited by monomorphic short-coupled extrasystoles from the right ventricular apex/lower free wall. Median survival in risk-haplotype haplotype-positives was 70 vs. 93 years for haplotype-negatives (P < .01), with a worse phenotype in males (median survival 63 vs. 83 years in females, P < .01). Implantable cardioverter-defibrillators were implanted in 99 patients (76 [77%] for primary prevention). Two arrhythmic events occurred in the primary prevention group during follow-up (5 ± 3 years).

Conclusion: Despite our extensive analysis, the complexity in identifying asymptomatic IVF family members at risk for future arrhythmias based on clinical parameters is once more demonstrated.

Keywords: DPP6; Idiopathic ventricular fibrillation; Sudden cardiac death.

MeSH terms

  • Cardiac Resynchronization Therapy
  • DNA / genetics*
  • Death, Sudden, Cardiac / epidemiology*
  • Death, Sudden, Cardiac / prevention & control
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / genetics*
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / metabolism
  • Electrocardiography*
  • Female
  • Haplotypes
  • Heart Ventricles / diagnostic imaging
  • Heart Ventricles / physiopathology*
  • Humans
  • Incidence
  • Magnetic Resonance Imaging, Cine / methods*
  • Male
  • Middle Aged
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Netherlands / epidemiology
  • Polymorphism, Genetic*
  • Potassium Channels / genetics*
  • Potassium Channels / metabolism
  • Primary Prevention / methods
  • Risk Factors
  • Survival Rate / trends
  • Ventricular Fibrillation / diagnosis
  • Ventricular Fibrillation / genetics*
  • Ventricular Fibrillation / physiopathology

Substances

  • Nerve Tissue Proteins
  • Potassium Channels
  • DNA
  • DPP6 protein, human
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases

Supplementary concepts

  • Paroxysmal ventricular fibrillation