Polymorphisms rs231775 and rs5742909 CTLA-4 gene and their associative relations with chronic HBV infection in children
https://doi.org/10.22627/2072-8107-2020-19-3-15-18
Abstract
The study of the genetic polymorphism rs231775 (+ 49A > G) and rs5742909 (+ 3 18С > Т) of the CTLA-4 gene in 100 children with chronic HBV infection revealed associations only with the carriage of the + 49A/ G polymorphic variant. Moreover, the carriage of the G allele in the homozygous mutant + 49GG position suggested the development of pronounced forms with a progressive course and a high probability of the outcome of the disease in cirrhosis.
The established gender differences — the boys' high expression of the minor G-allele of the CTLA-4 gene, especially in the homozygous mutant variation + 49GG — proves the phenomenon of a high incidence of hepatotropic viral infection in boys.
Therefore, the carriage of mutant variation + 49GG can be considered among the HOST factors for predicting adverse outcomes of chronic HBV infection in children.
About the Authors
F. I. InoyatovaUzbekistan
Flora Inoyatova - MD, Head of the Department of Hepatology.
Tashkent
G. Z. Inogamova
Uzbekistan
PhD
Tashkent
F. G. Abdullaevа
Uzbekistan
PhD
Tashkent
N. K. Valievа
Uzbekistan
PhD
Tashkent
N. A. Ikramova
Uzbekistan
Tashkent
H. M. Kadyrhodzhaevа
Uzbekistan
Tashkent
A. Kh. Akhmedovа
Uzbekistan
PhD
Tashkent
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Review
For citations:
Inoyatova F.I., Inogamova G.Z., Abdullaevа F.G., Valievа N.K., Ikramova N.A., Kadyrhodzhaevа H.M., Akhmedovа A.Kh. Polymorphisms rs231775 and rs5742909 CTLA-4 gene and their associative relations with chronic HBV infection in children. CHILDREN INFECTIONS. 2020;19(3):15-18. (In Russ.) https://doi.org/10.22627/2072-8107-2020-19-3-15-18