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(Circulation Research. 2004;95:e29.)
© 2004 American Heart Association, Inc.

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Association of Human Connexin40 Gene Polymorphisms With Atrial Vulnerability as a Risk Factor for Idiopathic Atrial Fibrillation

Mehran Firouzi, Hemanth Ramanna, Bart Kok, Habo J. Jongsma, Bobby P.C. Koeleman, Pieter A. Doevendans, W. Antoinette Groenewegen, Richard N.W. Hauer

From the Department of Medical Physiology (M.F., B.K., H.J.J., W.A.G.), University Medical Center Utrecht; Department of Cardiology (H.R., P.A.D., R.N.W.H.), University Medical Center Utrecht; Complex Genetics Group (B.P.C.K.), Department of Medical Genetics, University Medical Center Utrecht; and the Interuniversity Cardiology Institute of the Netherlands (P.A.D), Utrecht, The Netherlands.

Correspondence to Dr Habo Jongsma, University of Utrecht, Department of Medical Physiology, PO Box 85060, Utrecht 3508 AB, The Netherlands. E-mail h.j.jongsma{at}med.uu.nl

Alterations in distribution, density, and properties of cardiac gap junctions, which mediate electrical coupling of cardiomyocytes, are considered potentially arrhythmogenic. We recently reported 2 linked polymorphisms within regulatory regions of the gene for the atrial gap junction protein connexin40 (Cx40) at nucleotides –44 (GA) and +71 (AG), which were associated with familial atrial standstill. The present study examined whether these Cx40 polymorphisms were associated with increased atrial vulnerability in vivo and arrhythmia susceptibility. In 30 subjects without structural heart disease, of whom 14 had documented sporadic paroxysmal atrial fibrillation (AF) and 16 had no AF history, inducibility of AF was assessed using an increasingly aggressive atrial stimulation protocol. Coefficient of spatial dispersion of refractoriness (CD) was calculated. CD was defined as the SD of 12 local mean fibrillatory intervals recorded at right atrial sites, expressed as a percentage of the overall mean fibrillatory interval. Cx40 genotypes were determined by direct DNA sequencing. Subjects were stratified according to normal or increased CD with a cutoff value of 3.0, because CD >3.0 was previously shown to be strongly associated with enhanced atrial vulnerability. The prevalence of the minor Cx40 allele (–44A) and –44AA genotype was significantly higher in subjects with increased dispersion (n=13) compared with those with CD 3.0 (n=17; P=0.00046 and P=0.025; odds ratios of 6.7 and 7.4) and a control population (n=253; P=0.00002 and P=3.90x10^–7). Carriers of –44AA genotype had a significantly higher CD compared with those with –44GG genotype (6.37±1.21 versus 2.38±0.39, P=0.018), whereas heterozygotes had intermediate values (3.95±1.38, NS). All subjects with increased CD had a history of idiopathic AF compared with only 1 subject with normal CD. The –44A allele and –44AA genotype were significantly more frequent in subjects with prior AF than in those without (P=0.0019 and P=0.031; odds ratios 5.3 and 6.2). This study provides strong evidence linking Cx40 polymorphisms to enhanced atrial vulnerability and increased risk of AF. The full text of this article is available online at http://circres.ahajournals.org.

Key Words: arrhythmias • atrium • electrophysiology • gap junctions • genetics

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