Epistatic Effects of Potassium Channel Variation on Cardiac Repolarization and Atrial Fibrillation Risk
| Autor: | Diane Fatkin, Lina Karlsdotter, Lyn R. Griffiths, Robyn Otway, Monique Ohanian, Gunjan Trivedi, Bruce D. Walker, Prashanthan Sanders, Magdalena Soka, Robert A. Smith, Stefan A. Mann, Rajesh N. Subbiah, Dennis L. Kuchar, Merridee A. Wouters, Poonam Zodgekar, Jamie I. Vandenberg, Guanglan Guo |
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| Jazyk: | angličtina |
| Předmět: |
Adult
Male Proband Nonsynonymous substitution medicine.medical_specialty Patch-Clamp Techniques Adolescent Action Potentials Article Young Adult Heart Conduction System Internal medicine Atrial Fibrillation medicine Humans Repolarization Genetic Predisposition to Disease genetics Gene Aged Aged 80 and over Genetics atrial cell modeling business.industry Genetic Variation Epistasis Genetic Atrial fibrillation Sequence Analysis DNA Middle Aged medicine.disease potassium channels Phenotype Potassium channel Case-Control Studies Cardiology Female Cardiology and Cardiovascular Medicine business Familial atrial fibrillation familial atrial fibrillation |
| Zdroj: | Journal of the American College of Cardiology. (11):1017-1025 |
| ISSN: | 0735-1097 |
| DOI: | 10.1016/j.jacc.2011.11.039 |
| Popis: | ObjectivesThe aim of this study was to evaluate the role of cardiac K+ channel gene variants in families with atrial fibrillation (AF).BackgroundThe K+ channels play a major role in atrial repolarization but single mutations in cardiac K+ channel genes are infrequently present in AF families. The collective effect of background K+ channel variants of varying prevalence and effect size on the atrial substrate for AF is largely unexplored.MethodsGenes encoding the major cardiac K+ channels were resequenced in 80 AF probands. Nonsynonymous coding sequence variants identified in AF probands were evaluated in 240 control subjects. Novel variants were characterized using patch-clamp techniques and in silico modeling was performed using the Courtemanche atrial cell model.ResultsNineteen nonsynonymous variants in 9 genes were found, including 11 rare variants. Rare variants were more frequent in AF probands (18.8% vs. 4.2%, p < 0.001), and the mean number of variants was greater (0.21 vs. 0.04, p < 0.001). The majority of K+ channel variants individually had modest functional effects. Modeling simulations to evaluate combinations of K+ channel variants of varying population frequency indicated that simultaneous small perturbations of multiple current densities had nonlinear interactions and could result in substantial (>30 ms) shortening or lengthening of action potential duration as well as increased dispersion of repolarization.ConclusionsFamilies with AF show an excess of rare functional K+ channel gene variants of varying phenotypic effect size that may contribute to an atrial arrhythmogenic substrate. Atrial cell modeling is a useful tool to assess epistatic interactions between multiple variants. |
| Databáze: | OpenAIRE |
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