Skip to content

Genetic Risk Assessment of Defibrillator Events

Genetic Risk Assessment of Defibrillator Events: A Prospective Multicenter Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02045043
Acronym
GRADE
Enrollment
1807
Registered
2014-01-24
Start date
2002-03-31
Completion date
2012-06-30
Last updated
2014-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arrhythmias, Cardiomyopathy, Congestive Heart Failure, Sudden Cardiac Death

Keywords

Sudden Cardiac Death, Arrhythmias, Congestive Heart Failure, Cardiomyopathy, Single Nucleotide Polymorphisms, Genomics

Brief summary

Arrhythmias remain a major health problem, causing at least 250,000 deaths annually in the United States. Pharmacological treatments often do more harm than good, and device therapies are limited by high cost and effects on quality of life. Ion channel mutations cause rare inherited arrhythmopathies, but account for only a small fraction of patients with life- threatening arrhythmias and sudden death. Most arrhythmias occur during myocardial ischemia, following myocardial infarction, and in patients with poor left ventricular (LV) function of any etiology. Aside from ejection fraction (EF), few clinically useful indicators to stratify the risk of sudden death have been identified. The role of subtle difference in ion channel expression and/or structure in predisposing patients to arrhythmias and modulating the risk of sudden death is unknown. In this study, we are prospectively testing whether polymorphisms in ion channels and ion channel modifying genes are associated with arrhythmias in a population with internal cardioverter-defibrillators (ICDs) and poor LV function. We will test the hypothesis that functional polymorphisms in the coding sequences and promoter regions of cardiac genes (e.g. ion channels, beta-adrenergic receptors) predispose individuals to arrhythmias and /or heart failure progression. We hope to identify genetic predictors for the common forms of sudden cardiac death. This would allow the identification of a subpopulation of heart failure patients that would benefit most from ICD placement.

Interventions

None listed

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Iowa
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* An ICD placed during the last 5 years, or a planned ICD within 1 month * Age 18 or older * Left Ventricular Ejection fraction \< or = 30% * Ability to give informed consent

Exclusion criteria

* Patient refuses or is unable to give consent * A life expectancy \<6 months from a non-cardiac life threatening disease * Ongoing Class IV heart failure symptoms despite treatment * History of cardiac transplant or left ventricular assist device

Design outcomes

Primary

MeasureTime frameDescription
Shock-Free SurvivalUp to 5 yearsTime to first appropriate shock from an Implantable Cardioverter-Defibrillator

Secondary

MeasureTime frameDescription
SurvivalUp to 5 yearsTime to death from any cause
Transplant- and VAD-Free SurvivalUp to 5 yearsTime to occurence of death from any cause, cardiac transplantation, or Ventricular Assist Device placement (whichever comes first)
Appropriate Shock FrequencyUp to 5 yearsThe number of appropriate shocks per year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026