Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

Lasse S Ravn; Jacob Hofman-Bang; Ulrik Dixen; Severin Olesen Larsen; Gorm Jensen; Stig Haunsø; Jesper Hastrup Svendsen; Michael Christiansen

doi:10.1016/j.amjcard.2005.03.086

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

Lasse S Ravn, Jacob Hofman-Bang, Ulrik Dixen, Severin Olesen Larsen, Gorm Jensen, Stig Haunsø, Jesper Hastrup Svendsen, Michael Christiansen

67 Citations (Scopus)

Abstract

The 97T polymorphism of the KCNE5 gene, coding for an inhibitory beta-subunit, MiRP4, of the repolarizing cardiac potassium ion channel KCNQ1, was significantly more frequent in 96 controls than in 158 patients with atrial fibrillation (AF). KCNQ1 is involved in cardiac action potential, and increased function has been associated with AF. Because the KCNE5 gene is located on the X chromosome, the protection conferred by the 97T polymorphism may help explain the gender-related difference in the risk of AF.

Original language	English
Journal	American Journal of Cardiology
Volume	96
Issue number	3
Pages (from-to)	405-7
Number of pages	3
ISSN	0002-9149
DOIs	https://doi.org/10.1016/j.amjcard.2005.03.086
Publication status	Published - 1 Aug 2005

Keywords

Adult
Aged
Aged, 80 and over
Atrial Fibrillation
Case-Control Studies
Chi-Square Distribution
Female
Genotype
Humans
Male
Middle Aged
Polymorphism, Genetic
Potassium Channels, Voltage-Gated
Risk Assessment
Journal Article
Research Support, Non-U.S. Gov't

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10.1016/j.amjcard.2005.03.086

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Cite this

@article{0fb7f28c53824a60ae61afe63971aceb,

title = "Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation",

abstract = "The 97T polymorphism of the KCNE5 gene, coding for an inhibitory beta-subunit, MiRP4, of the repolarizing cardiac potassium ion channel KCNQ1, was significantly more frequent in 96 controls than in 158 patients with atrial fibrillation (AF). KCNQ1 is involved in cardiac action potential, and increased function has been associated with AF. Because the KCNE5 gene is located on the X chromosome, the protection conferred by the 97T polymorphism may help explain the gender-related difference in the risk of AF.",

keywords = "Adult, Aged, Aged, 80 and over, Atrial Fibrillation, Case-Control Studies, Chi-Square Distribution, Female, Genotype, Humans, Male, Middle Aged, Polymorphism, Genetic, Potassium Channels, Voltage-Gated, Risk Assessment, Journal Article, Research Support, Non-U.S. Gov't",

author = "Ravn, {Lasse S} and Jacob Hofman-Bang and Ulrik Dixen and Larsen, {Severin Olesen} and Gorm Jensen and Stig Hauns{\o} and Svendsen, {Jesper Hastrup} and Michael Christiansen",

year = "2005",

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day = "1",

doi = "10.1016/j.amjcard.2005.03.086",

language = "English",

volume = "96",

pages = "405--7",

journal = "American Journal of Cardiology",

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TY - JOUR

T1 - Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

AU - Ravn, Lasse S

AU - Hofman-Bang, Jacob

AU - Dixen, Ulrik

AU - Larsen, Severin Olesen

AU - Jensen, Gorm

AU - Haunsø, Stig

AU - Svendsen, Jesper Hastrup

AU - Christiansen, Michael

PY - 2005/8/1

Y1 - 2005/8/1

N2 - The 97T polymorphism of the KCNE5 gene, coding for an inhibitory beta-subunit, MiRP4, of the repolarizing cardiac potassium ion channel KCNQ1, was significantly more frequent in 96 controls than in 158 patients with atrial fibrillation (AF). KCNQ1 is involved in cardiac action potential, and increased function has been associated with AF. Because the KCNE5 gene is located on the X chromosome, the protection conferred by the 97T polymorphism may help explain the gender-related difference in the risk of AF.

AB - The 97T polymorphism of the KCNE5 gene, coding for an inhibitory beta-subunit, MiRP4, of the repolarizing cardiac potassium ion channel KCNQ1, was significantly more frequent in 96 controls than in 158 patients with atrial fibrillation (AF). KCNQ1 is involved in cardiac action potential, and increased function has been associated with AF. Because the KCNE5 gene is located on the X chromosome, the protection conferred by the 97T polymorphism may help explain the gender-related difference in the risk of AF.

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Atrial Fibrillation

KW - Case-Control Studies

KW - Chi-Square Distribution

KW - Female

KW - Genotype

KW - Humans

KW - Male

KW - Middle Aged

KW - Polymorphism, Genetic

KW - Potassium Channels, Voltage-Gated

KW - Risk Assessment

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1016/j.amjcard.2005.03.086

DO - 10.1016/j.amjcard.2005.03.086

M3 - Journal article

C2 - 16054468

SN - 0002-9149

VL - 96

SP - 405

EP - 407

JO - American Journal of Cardiology

JF - American Journal of Cardiology

IS - 3

ER -

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

Abstract

Keywords

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