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Am J Cardiol. 2014 Jan 15;113(2):309-13. doi: 10.1016/j.amjcard.2013.08.045. Epub 2013 Oct 3.

A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.

Author information

1
Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
2
Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee.
3
Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee.
4
Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: dawood.darbar@vanderbilt.edu.

Abstract

Single nucleotide polymorphisms (SNPs) at chromosome 4q25 (near PITX2) are strongly associated with atrial fibrillation (AF). We assessed whether a 4q25-tagging SNP (rs2200733) is associated with PR interval duration in patients with lone and typical AF and controls. Patients with lone (n = 169) and typical (n = 269) AF enrolled in the Vanderbilt AF registry and controls (n = 1,403) derived from the Vanderbilt DNA Biobank were studied. Carriage of the rs2200733T allele (CT or TT genotype) was more common in patients with lone (39%) than typical (25%) AF or controls (21%, p <0.01 for both comparisons). In both AF cohorts, we observed an association between genotype and PR interval duration (median PR interval for CC, CT, and TT: 162, 178, and 176 ms, respectively, for lone, p = 0.038 and 166, 180, and 196 ms, respectively, for typical, p = 0.001). After adjustment for covariates, the association between T allele and PR prolongation persisted, with mean effect size of 10.9, 12.8, and 4.4 ms for patients with lone and typical AF and controls, respectively (p <0.05 for each comparison). We found that a common 4q25 AF susceptibility allele (rs2200733) is associated with PR interval prolongation in patients with lone and typical AF and controls with no AF. Given that prolonged PR interval is an established risk factor for AF, this observation, in the context of previously described functional effects of PITX2 deficiency, provides further knowledge about the pathophysiological link of 4q25 variants with AF.

PMID:
24161141
PMCID:
PMC3947341
DOI:
10.1016/j.amjcard.2013.08.045
[Indexed for MEDLINE]
Free PMC Article

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