About this trial

Short-coupled ventricular fibrillation (SCVF) is a lethal, primary electrical disorder and an important cause of unexplained cardiac arrest.1 Recent work from our group suggests that a substantial proportion of SCVF cases is associated to circulating autoantibodies targeting TREK-1, a cardiac potassium channel, resulting in an abnormal gain-of-function which is the prerequisite for the SCVF phenotype.2 This proposal is a translational multicenter study to validate anti-TREK-1 autoantibodies as a diagnostic and prognostic biomarker in a large, diversified cohort of SCVF patients (Figure 1). Functional, cellular experiments in patient-derived hiPSC cardiomyocytes and Purkinje cells will be performed to explore the cell type-specific role of TREK-1 in arrhythmogenesis, while single-nuclear RNA sequencing (snRNA-seq) will allow us to establish the transcriptomic profile (Figure 1). These results will identify the cellular substrate for SCVF.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Diagnosis of SCVF as per current criteria

Willingness to provide written informed consent

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Repeat plasma screening for the presence or absence of anti-TREK-1 autoantibodies
  • DPP6 risk haplotype

Treatment groups

300 Participants
are divided into 3 treatment groups

Locations

5
Canada
St-Paul's Hospital - University of British Columbia VancouverBritish Columbia, Canada
PHRI HamiltonOntario, Canada
Ottawa Heart Center OttawaOntario, Canada
Institut universitaire de cardiologie et pneumologie de QuébecG1V4G5, QuébecQuebec, Canada

Sponsors and collaborators

Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

Lead sponsor