Role of IL13 genetic polymorphism in the development of bronchial asthma in children
https://doi.org/10.15789/1563-0625-ROI-1986
Abstract
Bronchial asthma is a multifactorial disease, with both environmental factors and genetic predisposal affecting its development. A number of gene associations have been obtained between polymorphisms of cytokine genes produced by different types of immune cells and asthma development. Interleukin-13 is involved in allergic inflammation, increased bronchial hypersensitivity, regulation of eosinophil levels and IgE production by B cells, thus making it promising for studying IL13 gene polymorphisms in bronchial asthma coupled to development of the disease. The aim of this study was to investigate possible association between asthma and IL13 rs1800925 polymorphism in the children of Caucasian origin in Eastern Siberia. Four groups of patients with asthma were examined (mean age 12.8±1.2 years): with a controlled (n = 95) and uncontrolled course (n = 107), with severe (n = 71) and moderate severity (n = 131) diseases. The control group consisted of healthy individuals: children (n = 33) and adults (n = 102). DNA was isolated with sorbent method; genotyping was carried out using RT-PCR using specific oligonucleotide primers and fluorescent TaqMan probes. The allele and genotype frequencies were compared by the χ-square test using an online calculator. The odds ratio (OR) with a 95% confidence interval (CI) was performed to link genetic markers with pathological phenotypes. The CT IL13 rs1800925 genotype was shown to be associated with moderate asthma and cases of uncontrollable clinical course, whereas the TT genotype was associated with severe asthma. Thus, rs1800925 polymorphism of IL13 gene (the T* variant is known to be associated with increased IL-13 expression) may be associated with bronchial asthma in children. Our data are consistent with results of other authors. E.g., Liu Z. et al. revealed an association between rs1800925 IL13 and the risk of developing asthma in children, with CT and TT genotypes being more common in the patient group. Radhakrishnan A. et al., was studied rs1800925 IL13 in adult population of Malaysia and found that the T* allele frequency in the group of patients significantly exceeds the frequency of this allele in the control group. Thus, the results of our study showed that IL13 rs1800925 polymorphism is associated with bronchial asthma in children, especially, with level of its control and severity of the disease.
About the Authors
S. Yu. TereschenkoRussian Federation
Tereshchenko Sergey Yu., PhD, MD (Medicine), Professor, Head, Clinical Department of Somatic and Mental Health in Children
Krasnoyarsk
M. V. Smolnikova
Russian Federation
Smolnikova Marina V., PhD (Biology), Leading Research Associate
660022, Krasnoyarsk, Partizan Zheleznyak str., 3g.
E. V. Kasparov
Russian Federation
Kasparov Eduard V., PhD, MD (Medicine), Professor, Director
Krasnoyarsk
E. V. Shakhtshneider
Shakhtshneider Elena V., PhD (Medicine), Deputy Director
Krasnoyarsk
M. A. Malinchik
Malinchik Marina A., Graduate Student
Krasnoyarsk
O. S. Konopleva
Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Konopleva Olga S., PhD (Medicine), Junior Research Associate, Research Institute of Medical Problems of the North, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences; Krasnoyarsk State V. Voino-Yasenetsky Medical University
Krasnoyarsk
S. V. Smirnova
Smirnova Svetlana V., PhD, MD (Medicine), Professor, Head of the Scientific Direction
Krasnoyarsk
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Review
For citations:
Tereschenko S.Yu., Smolnikova M.V., Kasparov E.V., Shakhtshneider E.V., Malinchik M.A., Konopleva O.S., Smirnova S.V. Role of IL13 genetic polymorphism in the development of bronchial asthma in children. Medical Immunology (Russia). 2020;22(5):907-914. (In Russ.) https://doi.org/10.15789/1563-0625-ROI-1986