| Literature DB >> 18504616 |
Santiago Reyes1, Andre Terzic, Douglas W Mahoney, Margaret M Redfield, Richard J Rodeheffer, Timothy M Olson.
Abstract
ATP-sensitive K+ (K(ATP)) channel mutations have been identified in individuals with dilated cardiomyopathy and overt heart failure. Here, a common E23K functional polymorphism in the Kir6.2 channel pore versus cardiac phenotype was studied in a cross-sectional community-based cohort (n = 2,031). The KK genotype was associated with greater left ventricular size among subjects with increased stress load due to hypertension. These findings implicate Kir6.2 K23 as a risk factor for adverse subclinical myocardial remodeling, and underscore the significance of cardiac K(ATP) channels within the population.Entities:
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Year: 2008 PMID: 18504616 PMCID: PMC2587318 DOI: 10.1007/s00439-008-0519-3
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132