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DOI: https://doi.org/10.22263/2312-4156.2017.2.70

Bubeshka D.A., Snezhitskiy V.A., Stepuro T.L.
The relationship of interleukin-10 gene polymorphism C-592A with interleukin-10 level and the risk of nonvalvular atrial fibrillation development
Grodno State Medical University, Grodno, Republic of Belarus

Vestnik VGMU. 2017;16(2):70-78.

Abstract.
Objectives. To study the distribution of genotypes and alleles frequencies of the polymorphic marker С-592А of interleukin-10 (IL-10) gene and to evaluate the relationship of the mentioned polymorphism with IL-10 plasma levels in patients of Grodno region with nonvalvular atrial fibrillation (AF) with ischemic heart disease (IHD) and/or arterial hypertension (AH), with ischemic heart disease and/or AH without the history of AF episodes and in patients without any cardiovascular diseases.
Material and methods. 105 patients with ischemic heart disease and/or arterial hypertension were examined. Among them there were 74 patients with persistent and permanent atrial fibrillation and 31 patients without AF episodes in their history. The control group included 37 patients without cardiovascular diseases and AF. IL-10 blood plasma levels were evaluated by ELISA test. The identification of polymorphism С-592А of IL-10 gene was performed using the polymerase chain reaction.
Results. It has been revealed that in the group of patients with AF the frequency of АА genotype and А allele was significantly higher than that in the group of patients with ischemic heart disease and/or arterial hypertension without AF episodes in their history f and also than that in the group of patients without any cardiovascular pathology. Nucleotide polymorphism association with the IL-10 level in plasma was revealed only in patients with AF and left ventricular systolic dysfunction. The maximum level of IL-10 was observed in patients with CC/CA genotype and C allele.
Conclusions. The presence of A allele in the genotype is associated with the 1,34-fold increase of nonvalvular AF development risk (95% CI 1,14-1,56), while the presence of AA genotype 1,48 times increases the risk of this disease development (95% CI 1,3-1,71) in patients with ischemic heart disease and/or arterial hypertension.
Key words: atrial fibrillation, interleukin -10, polymorphism С-592А.

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Information about authors:
Bubeshka D.A. – postgraduate of the Chair of Internal Medicine No.1, Grodno State Medical University;
Snezhitskiy V.A. – Doctor of Medical Sciences, corresponding member of the Belarusian National Academy of Sciences, rector, professor of the Chair of Internal Medicine No.1, Grodno State Medical University;
Stepuro T.L. – associate research officer of the Scientific-Research Laboratory of the Scientific-Research Department, Grodno State Medical University.

Correspondence address: Republic of Belarus, 230009, Grodno, 80 Gorky str., Grodno State Medical University, Chair of Internal Medicine No.1. E-mail: Этот адрес электронной почты защищён от спам-ботов. У вас должен быть включен JavaScript для просмотра. – Darya A. Bubeshka.

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