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Polymorphisms in the GNAS Gene as Predictors of Ventricular Tachyarrhythmias and Sudden Cardiac Death: Results From the DISCOVERY Trial and Oregon Sudden Unexpected Death Study.
- Source :
-
Journal of the American Heart Association [J Am Heart Assoc] 2016 Nov 28; Vol. 5 (12). Date of Electronic Publication: 2016 Nov 28. - Publication Year :
- 2016
-
Abstract
- Background: Population-based studies suggest that genetic factors contribute to sudden cardiac death (SCD).<br />Methods and Results: In the first part of the present study (Diagnostic Data Influence on Disease Management and Relation of Genetic Polymorphisms to Ventricular Tachy-arrhythmia in ICD Patients [DISCOVERY] trial) Cox regression was done to determine if 7 single-nucleotide polymorphisms (SNPs) in 3 genes coding G-protein subunits (GNB3, GNAQ, GNAS) were associated with ventricular tachyarrhythmia (VT) in 1145 patients receiving an implantable cardioverter-defibrillator (ICD). In the second part of the study, SNPs significantly associated with VT were further investigated in 1335 subjects from the Oregon SUDS, a community-based study analyzing causes of SCD. In the DISCOVERY trial, genotypes of 2 SNPs in the GNAS gene were nominally significant in the prospective screening and significantly associated with VT when viewed as recessive traits in post hoc analyses (TT vs CC/CT in c.393C>T: HR 1.42 [CI 1.11-1.80], P=0.005; TT vs CC/CT in c.2273C>T: HR 1.57 [CI 1.18-2.09], P=0.002). TT genotype in either SNP was associated with a HR of 1.58 (CI 1.26-1.99) (P=0.0001). In the Oregon SUDS cohort significant evidence for association with SCD was observed for GNAS c.393C>T under the additive (P=0.039, OR=1.21 [CI 1.05-1.45]) and recessive (P=0.01, OR=1.52 [CI 1.10-2.13]) genetic models.<br />Conclusions: GNAS harbors 2 SNPs that were associated with an increased risk for VT in ICD patients, of which 1 was successfully replicated in a community-based population of SCD cases. To the best of our knowledge, this is the first example of a gene variant identified by ICD VT monitoring as a surrogate parameter for SCD and also confirmed in the general population.<br />Clinical Trial Registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00478933.<br /> (© 2016 The Authors and Medtronic. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell.)
- Subjects :
- Aged
Cohort Studies
Defibrillators, Implantable
Female
Heart Failure complications
Humans
Male
Middle Aged
Polymorphism, Single Nucleotide
Proportional Hazards Models
Tachycardia, Ventricular etiology
Tachycardia, Ventricular therapy
Ventricular Fibrillation etiology
Ventricular Fibrillation therapy
Chromogranins genetics
Death, Sudden, Cardiac etiology
GTP-Binding Protein alpha Subunits, Gs genetics
Heart Failure physiopathology
Tachycardia, Ventricular genetics
Ventricular Fibrillation genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2047-9980
- Volume :
- 5
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of the American Heart Association
- Publication Type :
- Academic Journal
- Accession number :
- 27895044
- Full Text :
- https://doi.org/10.1161/JAHA.116.003905