Literature DB >> 18426444

Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia.

Yu Zhang1, Bingxi Chang, Songnian Hu, Duenmei Wang, Quan Fang, Xianyong Huang, Qiang Zeng, Ming Qi.   

Abstract

BACKGROUND: Many studies revealed that variations in cardiac ion channels would cause cardiac arrhythmias or act as genetic risk factors. We hypothesized that specific single nucleotide polymorphisms in cardiac ion channels were associated with cardiac rhythm disturbance in the Chinese population.
METHOD: We analyzed 160 nonfamilial cardiac arrhythmia patients and 176 healthy individuals from which 81 individuals were selected for association study, and a total of 19 previously reported SNPs in four cardiac ion channel genes (KCNQ1, KCNH2, SCN5A, KCNE1) were genotyped.
RESULTS: The frequency of KCNQ1 1638G>A, as well as the haplotype harboring KCNQ1 1638A, KCNQ1 1685 + 23G and 1732 + 43T (haplotype AGT) was significantly higher in healthy controls than in arrhythmia patients. This finding implicated that this haplotype (AGT) might be a protective factor against arrhythmias.
CONCLUSIONS: Our study provided important information to elucidate the effect of SNPs of cardiac ion channel genes on channel function and susceptibility to cardiac arrhythmias in Chinese population.

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Year:  2008        PMID: 18426444      PMCID: PMC6932127          DOI: 10.1111/j.1542-474X.2008.00220.x

Source DB:  PubMed          Journal:  Ann Noninvasive Electrocardiol        ISSN: 1082-720X            Impact factor:   1.468


  28 in total

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2.  Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.

Authors:  H Iwasa; T Itoh; R Nagai; Y Nakamura; T Tanaka
Journal:  J Hum Genet       Date:  2000       Impact factor: 3.172

3.  The relationship between third-codon position nucleotide content, codon bias, mRNA secondary structure and gene expression in the drosophilid alcohol dehydrogenase genes Adh and Adhr.

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Journal:  Genetics       Date:  2001-10       Impact factor: 4.562

4.  A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.

Authors:  N Schmitt; M Schwarz; A Peretz; I Abitbol; B Attali; O Pongs
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

5.  Single nucleotide polymorphism map of five long-QT genes.

Authors:  Atakan Aydin; Sylvia Bähring; Stefan Dahm; Ulf P Guenther; Regina Uhlmann; Andreas Busjahn; Friedrich C Luft
Journal:  J Mol Med (Berl)       Date:  2004-12-15       Impact factor: 4.599

6.  Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families.

Authors:  Y Friedlander; M Vatta; N Sotoodehnia; R Sinnreich; H Li; O Manor; J A Towbin; D S Siscovick; J D Kark
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7.  Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization.

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Review 8.  Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias.

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9.  Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation.

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Journal:  Am Heart J       Date:  2002-09       Impact factor: 4.749

10.  A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation.

Authors:  Prakash C Viswanathan; D Woodrow Benson; Jeffrey R Balser
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  3 in total

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Journal:  PLoS One       Date:  2012-03-29       Impact factor: 3.240

2.  Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants.

Authors:  Mel Lina Pinsach-Abuin; Bernat Del Olmo; Adrian Pérez-Agustin; Jesus Mates; Catarina Allegue; Anna Iglesias; Qi Ma; Daria Merkurjev; Sergiy Konovalov; Jing Zhang; Farah Sheikh; Amalio Telenti; Josep Brugada; Ramon Brugada; Melissa Gymrek; Julia di Iulio; Ivan Garcia-Bassets; Sara Pagans
Journal:  Cell Rep Med       Date:  2021-04-20

3.  Effects of Mexiletine on a Race-specific Mutation in Nav1.5 Associated With Long QT Syndrome.

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  3 in total

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