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The association analysis of polymorphisms G590A of the NAT2 gene and С3435Т of the ABCB1 gene with isolated of ventricular septal defect in children from Krasnodar region

Abstract

The associations between polymorphisms of G590A of the NAT2 gene and С3435T of the ABCB1 gene and the risk of isolated ventricular septal defect in children from Krasnodar region were studied. It failed to find out the clear trend to accumulation of 590GG NAT2 and 3435TT ABCB1 mutant genotypes, supposedly associated with this nosology. In studying the allely frequencies and genotypes of these polymorphisms, it was not revealed the statistically significant differences between groups of the patients with ventricular septal defect and control group, depending on sex. The data analysis of the pair combinations of the tested polymorphisms did not allowed to reveal the statistically significant differences, but the clear trend was observed in accumulation of 590GG/3435ТТ genotypes in the group of children with ventricular septal defect (OR=4.02, 95% CI=0.94-17.5, χ2 =4.08, р=0.04). No associations of the polymorphisms with isolated ventricular septal defect were found.

About the Authors

O. P. Brayko
Kuban State Medical University
Russian Federation


K. Yu. Lazarev
Kuban State Medical University
Russian Federation


Ya. D. Shvetsov
Kursk State Medical University
Russian Federation


V. I. Golubtsov
Kuban State Medical University
Russian Federation


A. V. Polonikov
Kursk State Medical University
Russian Federation


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Review

For citations:


Brayko O.P., Lazarev K.Yu., Shvetsov Ya.D., Golubtsov V.I., Polonikov A.V. The association analysis of polymorphisms G590A of the NAT2 gene and С3435Т of the ABCB1 gene with isolated of ventricular septal defect in children from Krasnodar region. Kursk Scientific and Practical Bulletin "Man and His Health". 2013;(4):15-20.

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ISSN 1998-5746 (Print)
ISSN 1998-5754 (Online)