Association between Allelic Variants of IL2, IL2RA, and IL7R Genes and Multiple Sclerosis

Multiple sclerosis is a chronic progressive disease of nervous system caused by a combination of genetic and environmental factors leading to the development of a complex of autoimmune and neurodegenerative processes. We performed the analysis of association between multiple sclerosis and polymorphi...

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Bibliographic Details
Published in:Russian journal of genetics Vol. 55; no. 4; pp. 487 - 494
Main Authors: Timasheva, Y. R., Zaplakhova, O. V., Nasibullin, T. R., Tuktarova, I. A., Erdman, V. V., Bakhtiiarova, K. Z., Mustafina, O. E.
Format: Journal Article
Language:English
Published: Moscow Pleiades Publishing 01-04-2019
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Summary:Multiple sclerosis is a chronic progressive disease of nervous system caused by a combination of genetic and environmental factors leading to the development of a complex of autoimmune and neurodegenerative processes. We performed the analysis of association between multiple sclerosis and polymorphic markers of interleukin-2 ( IL2 ), interleukin-2 receptor alpha chain ( IL2A ) and interleukin-7 receptor alpha chain ( IL7R ) in the group of Russians, Tatars, and Bashkirs from the Republic of Bashkortostan ( N = 1620). In the total study group, we detected the association of IL7R rs10624573*I (OR = 0.79, P Bonf = 0.018) and rs1494558*T (OR = 1.44, P Bonf = 2.33 × 10 –4 ) variants with multiple sclerosis. When analyzed separately according to the ethnic origin, the association with IL7R rs1494558*T (OR = 1.49, P Bonf = 0.005) remained significant in the group of Russians, and the association of IL7R rs10624573*I remained significant in the group of Bashkirs (OR = 0.56, P Bonf = 0.02). We performed the multilocus analysis of association using the APSampler algorithm, and found seven combinations of the alleles and/or genotypes of the studied polymorphic loci, significantly associated with multiple sclerosis, most frequently including IL7R rs1494558 and IL7R rs10624573 allelic variants.
ISSN:1022-7954
1608-3369
DOI:10.1134/S1022795419030153