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Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes

Autoimmune thyroid diseases (AITDs) which include Graves' disease (GD) and Hashimoto's thyroiditis (HT) as well as type 1 diabetes (T1D) are common autoimmune disorders in children. Many genes are involved in the modulation of the immune system and their polymorphisms might predispose to a...

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Autores principales: Borysewicz-Sańczyk, Hanna, Sawicka, Beata, Wawrusiewicz-Kurylonek, Natalia, Głowińska-Olszewska, Barbara, Kadłubiska, Anna, Gościk, Joanna, Szadkowska, Agnieszka, Łosiewicz, Aleksandra, Młynarski, Wojciech, Kretowski, Adam, Bossowski, Artur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473350/
https://www.ncbi.nlm.nih.gov/pubmed/32974248
http://dx.doi.org/10.3389/fped.2020.00481
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author Borysewicz-Sańczyk, Hanna
Sawicka, Beata
Wawrusiewicz-Kurylonek, Natalia
Głowińska-Olszewska, Barbara
Kadłubiska, Anna
Gościk, Joanna
Szadkowska, Agnieszka
Łosiewicz, Aleksandra
Młynarski, Wojciech
Kretowski, Adam
Bossowski, Artur
author_facet Borysewicz-Sańczyk, Hanna
Sawicka, Beata
Wawrusiewicz-Kurylonek, Natalia
Głowińska-Olszewska, Barbara
Kadłubiska, Anna
Gościk, Joanna
Szadkowska, Agnieszka
Łosiewicz, Aleksandra
Młynarski, Wojciech
Kretowski, Adam
Bossowski, Artur
author_sort Borysewicz-Sańczyk, Hanna
collection PubMed
description Autoimmune thyroid diseases (AITDs) which include Graves' disease (GD) and Hashimoto's thyroiditis (HT) as well as type 1 diabetes (T1D) are common autoimmune disorders in children. Many genes are involved in the modulation of the immune system and their polymorphisms might predispose to autoimmune diseases development. According to the literature genes encoding IL2RA (alpha subunit of Interleukin 2 receptor), IFIH1 (Interferon induced with helicase C domain 1) and CTLA-4 (cytotoxic T cell antigen 4) might be associated with autoimmune diseases pathogenesis. The aim of the study was to assess the association of chosen single nucleotide polymorphisms (SNPs) of IL2RA, IFIH1, and CTLA-4 genes in the group of Polish children with AITDs and in children with T1D. We analyzed single nucleotide polymorphisms (SNPs) in the IL2RA region (rs7093069), IFIH1 region (rs1990760) and CTLA-4 region (rs231775) in group of Polish children and adolescents with type 1 diabetes (n = 194) and autoimmune thyroid diseases (GD n = 170, HT n = 81) and healthy age and sex matched controls for comparison (n = 110). There were significant differences observed between T1D patients and control group in alleles of IL2RA (rs7093069 T > C) and CTLA-4 (rs231775 G > A). In addition, the study revealed T/T genotype at the IL2RA locus (rs7093069) and G/G genotype at the CTLA-4 locus (rs231775) to be statistically significant more frequent in children with T1D. Moreover, genotypes C/T and T/T at the IFIH1 locus (rs1990760) were significantly more frequent in patients with T1D than in controls. We observed no significant differences between AITD patients and a control group in analyzed SNPs. In conclusion, we detected that each allele T of rs7093069 SNP at the IL2RA locus and G allele of rs231775 SNP at the CTLA-4 locus as well as C/T and T/T genotypes of rs1990760 SNP at the IFIH1 locus are predisposing in terms of T1D development. Thereby, we confirmed that IL2RA, IFIH1, and CTLA-4 gene locus have a role in T1D susceptibility. The analysis of selected SNPs revealed no association with AITDs in a group of Polish children and adolescents.
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spelling pubmed-74733502020-09-23 Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes Borysewicz-Sańczyk, Hanna Sawicka, Beata Wawrusiewicz-Kurylonek, Natalia Głowińska-Olszewska, Barbara Kadłubiska, Anna Gościk, Joanna Szadkowska, Agnieszka Łosiewicz, Aleksandra Młynarski, Wojciech Kretowski, Adam Bossowski, Artur Front Pediatr Pediatrics Autoimmune thyroid diseases (AITDs) which include Graves' disease (GD) and Hashimoto's thyroiditis (HT) as well as type 1 diabetes (T1D) are common autoimmune disorders in children. Many genes are involved in the modulation of the immune system and their polymorphisms might predispose to autoimmune diseases development. According to the literature genes encoding IL2RA (alpha subunit of Interleukin 2 receptor), IFIH1 (Interferon induced with helicase C domain 1) and CTLA-4 (cytotoxic T cell antigen 4) might be associated with autoimmune diseases pathogenesis. The aim of the study was to assess the association of chosen single nucleotide polymorphisms (SNPs) of IL2RA, IFIH1, and CTLA-4 genes in the group of Polish children with AITDs and in children with T1D. We analyzed single nucleotide polymorphisms (SNPs) in the IL2RA region (rs7093069), IFIH1 region (rs1990760) and CTLA-4 region (rs231775) in group of Polish children and adolescents with type 1 diabetes (n = 194) and autoimmune thyroid diseases (GD n = 170, HT n = 81) and healthy age and sex matched controls for comparison (n = 110). There were significant differences observed between T1D patients and control group in alleles of IL2RA (rs7093069 T > C) and CTLA-4 (rs231775 G > A). In addition, the study revealed T/T genotype at the IL2RA locus (rs7093069) and G/G genotype at the CTLA-4 locus (rs231775) to be statistically significant more frequent in children with T1D. Moreover, genotypes C/T and T/T at the IFIH1 locus (rs1990760) were significantly more frequent in patients with T1D than in controls. We observed no significant differences between AITD patients and a control group in analyzed SNPs. In conclusion, we detected that each allele T of rs7093069 SNP at the IL2RA locus and G allele of rs231775 SNP at the CTLA-4 locus as well as C/T and T/T genotypes of rs1990760 SNP at the IFIH1 locus are predisposing in terms of T1D development. Thereby, we confirmed that IL2RA, IFIH1, and CTLA-4 gene locus have a role in T1D susceptibility. The analysis of selected SNPs revealed no association with AITDs in a group of Polish children and adolescents. Frontiers Media S.A. 2020-08-21 /pmc/articles/PMC7473350/ /pubmed/32974248 http://dx.doi.org/10.3389/fped.2020.00481 Text en Copyright © 2020 Borysewicz-Sańczyk, Sawicka, Wawrusiewicz-Kurylonek, Głowińska-Olszewska, Kadłubiska, Gościk, Szadkowska, Łosiewicz, Młynarski, Kretowski and Bossowski. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Borysewicz-Sańczyk, Hanna
Sawicka, Beata
Wawrusiewicz-Kurylonek, Natalia
Głowińska-Olszewska, Barbara
Kadłubiska, Anna
Gościk, Joanna
Szadkowska, Agnieszka
Łosiewicz, Aleksandra
Młynarski, Wojciech
Kretowski, Adam
Bossowski, Artur
Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title_full Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title_fullStr Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title_full_unstemmed Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title_short Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes
title_sort genetic association study of il2ra, ifih1, and ctla-4 polymorphisms with autoimmune thyroid diseases and type 1 diabetes
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473350/
https://www.ncbi.nlm.nih.gov/pubmed/32974248
http://dx.doi.org/10.3389/fped.2020.00481
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