open access

Vol 64, No 11 (2006)
Other
Published online: 2006-12-04
Submitted: 2012-12-28
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Original article
MinK gene polymorphism in the pathogenesis of lone atrial fibrillation

Andrzej Prystupa, Grzegorz Dzida, Wojciech Myśliński, Grzegorz Małaj, Tomasz Lorenc
Kardiol Pol 2006;64(11):1205-1211.

open access

Vol 64, No 11 (2006)
Other
Published online: 2006-12-04
Submitted: 2012-12-28

Abstract


Introduction: Atrial fibrillation (AF) is the most common type of complex arrhythmia found in everyday clinical practice. Lone AF is a particular form occurring in 2% to 31% of patients with confirmed AF. Genetic factors may underline this arrhythmia.
Aim: To determine the relationship between G38S polymorphism in the MinK gene and the incidence of lone AF, and to evaluate this polymorphism as a genetic marker of susceptibility to AF.
Methods: The study involved 69 patients with lone AF and 60 control healthy subjects. Both groups included patients aged up to 65 years without cardiovascular or thyroid disease. MinK genotype was determined with PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism). The MinK gene was present in two allelic forms: G and S.
Results: The MinK G allele was found significantly more often in patients with AF (62.32%) compared to control subjects (41.80%) (p=0.009). In the AF group GS occurred more frequently (55.07%) than GG (34.78%) and SS genotypes (10.14%). In a logistic regression model the presence of G variant was associated with increase of AF risk in the study population (OR 2.39; 95% CI 0.88-6.54; p=0.084). Presence of GG genotype was associated with significant, over 10-fold, increase of AF risk. Presence of S allele of the MinK gene met criteria of protective factor against AF in the study population.
Conclusions: 1. G38S polymorphism in the MinK gene seems to be associated with incidence of lone AF in the study population. 2. GG genotype carrier state may significantly relate to increased risk of AF in the study group. 3. G38S

Abstract


Introduction: Atrial fibrillation (AF) is the most common type of complex arrhythmia found in everyday clinical practice. Lone AF is a particular form occurring in 2% to 31% of patients with confirmed AF. Genetic factors may underline this arrhythmia.
Aim: To determine the relationship between G38S polymorphism in the MinK gene and the incidence of lone AF, and to evaluate this polymorphism as a genetic marker of susceptibility to AF.
Methods: The study involved 69 patients with lone AF and 60 control healthy subjects. Both groups included patients aged up to 65 years without cardiovascular or thyroid disease. MinK genotype was determined with PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism). The MinK gene was present in two allelic forms: G and S.
Results: The MinK G allele was found significantly more often in patients with AF (62.32%) compared to control subjects (41.80%) (p=0.009). In the AF group GS occurred more frequently (55.07%) than GG (34.78%) and SS genotypes (10.14%). In a logistic regression model the presence of G variant was associated with increase of AF risk in the study population (OR 2.39; 95% CI 0.88-6.54; p=0.084). Presence of GG genotype was associated with significant, over 10-fold, increase of AF risk. Presence of S allele of the MinK gene met criteria of protective factor against AF in the study population.
Conclusions: 1. G38S polymorphism in the MinK gene seems to be associated with incidence of lone AF in the study population. 2. GG genotype carrier state may significantly relate to increased risk of AF in the study group. 3. G38S
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Keywords

polymorphism in the MinK gene could be used as a genetic marker of risk of lone AF. atrial fibrillation; genetics; MinK gene polymorphism

About this article
Title

Original article
MinK gene polymorphism in the pathogenesis of lone atrial fibrillation

Journal

Kardiologia Polska (Polish Heart Journal)

Issue

Vol 64, No 11 (2006)

Pages

1205-1211

Published online

2006-12-04

Bibliographic record

Kardiol Pol 2006;64(11):1205-1211.

Keywords

polymorphism in the MinK gene could be used as a genetic marker of risk of lone AF. atrial fibrillation
genetics
MinK gene polymorphism

Authors

Andrzej Prystupa
Grzegorz Dzida
Wojciech Myśliński
Grzegorz Małaj
Tomasz Lorenc

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