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Original Research

The Single Nucleotide Polymorphisms of IKs Potassium Channel Genes and Their Association with Atrial Fibrillation in a Chinese Population

Zeng Z.a, b · Tan C.a · Teng S.a · Chen J.c, d · Su S.c · Zhou X.c · Wang F.a · Zhang S.a · Gu D.c, d · Makielski J.C.e · Pu J.a

Author affiliations

aCenter for Arrhythmia Diagnosis and Treatment, cDivision of Population Genetics and Prevention, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, dNational Human Genome Center at Beijing, Beijing, bThe First Affiliated Hospital of Nanjing Medical University, Nanjing, China; eDepartment of Medicine/Cardiology, University of Wisconsin, Madison, Wisc., USA

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Cardiology 2007;108:97–103

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Article / Publication Details

First-Page Preview
Abstract of Original Research

Received: August 18, 2005
Accepted: June 19, 2006
Published online: September 29, 2006
Issue release date: August 2007

Number of Print Pages: 7
Number of Figures: 0
Number of Tables: 6

ISSN: 0008-6312 (Print)
eISSN: 1421-9751 (Online)

For additional information: https://www.karger.com/CRD

Abstract

Recent studies suggest that genetic mutation of the slow delayed rectifier potassium channel (IKs) may underlie atrial fibrillation (AF). We investigated the association between AF and the single nucleotide polymorphisms (SNPs) of genes KCNQ1, KCNE1 and KCNE4 associated with this channel. Common non-synonymous SNPs in KCNQ1 and KCNE1 known to be frequent in Asian people were selected and direct sequencing of KCNE4 was performed to identify possible SNPs. The AF group consisted of 142 hospitalized patients with AF, the community control group consisted of 120 subjects, and a ward control group consisted of 118 hospitalized patients without AF. Restriction fragment length polymorphism analysis was performed to determine the genotypes. The minor allele frequencies of P448R, R519H, G643S for KCNQ1 and G38S and D85N for KCNE1 in the AF group, the community control group and the ward control group were 9.9, 7.9, 9.3%; 0, 0, –; 4.3, 4.2, 1.7%; 28.4, 31.7, 29.7%; 0.7, 0.4%, –, respectively. There was no significant association between these SNPs and AF phenotype. There were eight SNPs in the whole length of KCNE4 plus 1,000 bases upstream of this gene including the non-synonymous SNP E145D. Logistical regression analysis revealed a difference in the distribution of KCNE4 E145D in the AF and the community control group (minor allele frequency was 34.0 versus 27.1% respectively, OR = 1.66, p = 0.044). We provided the frequencies of non-synonymous SNPs of KCNQ1 and KCNE1 in Chinese population; none of these SNPs was associated with AF. But KCNE4 E145D may be associated with the AF phenotype.

© 2007 S. Karger AG, Basel


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Article / Publication Details

First-Page Preview
Abstract of Original Research

Received: August 18, 2005
Accepted: June 19, 2006
Published online: September 29, 2006
Issue release date: August 2007

Number of Print Pages: 7
Number of Figures: 0
Number of Tables: 6

ISSN: 0008-6312 (Print)
eISSN: 1421-9751 (Online)

For additional information: https://www.karger.com/CRD


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