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A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.
- Source :
-
Heart rhythm [Heart Rhythm] 2012 Jul; Vol. 9 (7), pp. 1099-103. Date of Electronic Publication: 2012 Feb 15. - Publication Year :
- 2012
-
Abstract
- Background: T-peak to T-end (TPE) interval on the electrocardiogram is a measure of myocardial dispersion of repolarization and is associated with an increased risk of ventricular arrhythmias. The genetic factors affecting the TPE interval are largely unknown.<br />Objective: To identify common genetic variants that affect the duration of the TPE interval in the general population.<br />Methods: We performed a genome-wide association study on 1870 individuals of Finnish origin participating in the Health 2000 Study. The TPE interval was measured from T-peak to T-wave end in leads II, V(2), and V(5) on resting electrocardiograms, and the mean of these TPE intervals was adjusted for age, sex, and Cornell voltage-duration product. We sought replication for a genome-wide significant result in the 3745 subjects from the Framingham Heart Study.<br />Results: We identified a locus on 17q24 that was associated with the TPE interval. The minor allele of the common variant rs7219669 was associated with a 1.8-ms shortening of the TPE interval (P = 1.1 × 10(-10)). The association was replicated in the Framingham Heart Study (-1.5 ms; P = 1.3 × 10(-4)). The overall effect estimate of rs7219669 in the 2 studies was -1.7 ms (P = 5.7 × 10(-14)). The common variant rs7219669 maps downstream of the KCNJ2 gene, in which rare mutations cause congenital long and short QT syndromes.<br />Conclusion: The common variant rs7219669 is associated with the TPE interval and is thus a candidate to modify repolarization-related arrhythmia susceptibility in individuals carrying the major allele of this polymorphism.<br /> (Copyright © 2012 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adult
Asian People genetics
DNA Methylation
Electrocardiography
Electrophysiologic Techniques, Cardiac
Female
Finland
GC Rich Sequence genetics
Genetic Predisposition to Disease genetics
Genome-Wide Association Study
Humans
Male
Middle Aged
Heart Conduction System physiopathology
Long QT Syndrome genetics
Polymorphism, Single Nucleotide
Potassium Channels, Inwardly Rectifying genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1556-3871
- Volume :
- 9
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Heart rhythm
- Publication Type :
- Academic Journal
- Accession number :
- 22342860
- Full Text :
- https://doi.org/10.1016/j.hrthm.2012.02.019