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Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis

INTRODUCTION: Interleukin (IL)-33 is a proinflammatory cytokine contributing to the pathogenesis of rheumatoid arthritis (RA). The gene encoding IL-33 may serve as a genetic factor and be associated with the risk of RA. To investigate the potential association between IL33 and RA, we performed a cas...

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Autores principales: Li, Chun, Mu, Rong, Guo, Jianping, Wu, Xinyu, Tu, Xin, Liu, Xu, Hu, Fanlei, Guo, Shiwei, Zhu, Jiaxin, Xu, Huji, Li, Zhanguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075243/
https://www.ncbi.nlm.nih.gov/pubmed/24779919
http://dx.doi.org/10.1186/ar4554
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author Li, Chun
Mu, Rong
Guo, Jianping
Wu, Xinyu
Tu, Xin
Liu, Xu
Hu, Fanlei
Guo, Shiwei
Zhu, Jiaxin
Xu, Huji
Li, Zhanguo
author_facet Li, Chun
Mu, Rong
Guo, Jianping
Wu, Xinyu
Tu, Xin
Liu, Xu
Hu, Fanlei
Guo, Shiwei
Zhu, Jiaxin
Xu, Huji
Li, Zhanguo
author_sort Li, Chun
collection PubMed
description INTRODUCTION: Interleukin (IL)-33 is a proinflammatory cytokine contributing to the pathogenesis of rheumatoid arthritis (RA). The gene encoding IL-33 may serve as a genetic factor and be associated with the risk of RA. To investigate the potential association between IL33 and RA, we performed a case–control study based on Chinese Han population. METHODS: A three-stage case–control study was performed. Two tag single-nucleotide polymorphisms (SNPs) (rs7044343 and rs10975514), mapping to the IL33 gene, were first genotyped in the discovery population. We further genotyped rs7044343 and rs10975514 in the validation and replication population. The associations between the two tag SNPs and phenotypic subgroups of RA and levels of serum IL-33 were assessed with a logistic regression model. RESULTS: In the discovery population, the CC genotype of rs7044343 was associated with RA patients (odds ratio (OR) = 0.777, 95% confidence interval (CI), 0.611 to 0.988; P = 0.040). After anti-citrullinated peptide antibody (ACPA) stratification, the CC genotype of rs7044343 was also shown to be a protective genotype in RA without ACPA (OR = 0.610; 95% CI, 0.379 to 0.982; P = 0.042). In the validation population and replication population, the association between rs7044343 and RA, especially ACPA-negative RA, was still significant. A meta-analysis of discovery, validation, and replication panels confirmed the association between CC genotype of rs7044343 and RA (P(combined) = 0.0004; OR(combined) = 0.77; 95% CI, 0.67 to 0.89). No evidence was found for heterogeneity between three sample sets (P(het) = 0.99; I(2) = 0%). Similar results were also obtained in ACPA-negative RA (P(combined) = 0.0002; OR(combined) = 0.57; 95% CI, 0.43 to 0.77). No association was detected between rs10975514 polymorphism and RA susceptibility in the discovery and validation population. The serum levels of IL-33 were significantly lower in the patients with the rs7044343 CC genotype. CONCLUSION: The CC genotype of rs7044343 in IL33 is associated with RA patients and downregulates IL-33 expression in RA.
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spelling pubmed-40752432014-07-01 Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis Li, Chun Mu, Rong Guo, Jianping Wu, Xinyu Tu, Xin Liu, Xu Hu, Fanlei Guo, Shiwei Zhu, Jiaxin Xu, Huji Li, Zhanguo Arthritis Res Ther Research Article INTRODUCTION: Interleukin (IL)-33 is a proinflammatory cytokine contributing to the pathogenesis of rheumatoid arthritis (RA). The gene encoding IL-33 may serve as a genetic factor and be associated with the risk of RA. To investigate the potential association between IL33 and RA, we performed a case–control study based on Chinese Han population. METHODS: A three-stage case–control study was performed. Two tag single-nucleotide polymorphisms (SNPs) (rs7044343 and rs10975514), mapping to the IL33 gene, were first genotyped in the discovery population. We further genotyped rs7044343 and rs10975514 in the validation and replication population. The associations between the two tag SNPs and phenotypic subgroups of RA and levels of serum IL-33 were assessed with a logistic regression model. RESULTS: In the discovery population, the CC genotype of rs7044343 was associated with RA patients (odds ratio (OR) = 0.777, 95% confidence interval (CI), 0.611 to 0.988; P = 0.040). After anti-citrullinated peptide antibody (ACPA) stratification, the CC genotype of rs7044343 was also shown to be a protective genotype in RA without ACPA (OR = 0.610; 95% CI, 0.379 to 0.982; P = 0.042). In the validation population and replication population, the association between rs7044343 and RA, especially ACPA-negative RA, was still significant. A meta-analysis of discovery, validation, and replication panels confirmed the association between CC genotype of rs7044343 and RA (P(combined) = 0.0004; OR(combined) = 0.77; 95% CI, 0.67 to 0.89). No evidence was found for heterogeneity between three sample sets (P(het) = 0.99; I(2) = 0%). Similar results were also obtained in ACPA-negative RA (P(combined) = 0.0002; OR(combined) = 0.57; 95% CI, 0.43 to 0.77). No association was detected between rs10975514 polymorphism and RA susceptibility in the discovery and validation population. The serum levels of IL-33 were significantly lower in the patients with the rs7044343 CC genotype. CONCLUSION: The CC genotype of rs7044343 in IL33 is associated with RA patients and downregulates IL-33 expression in RA. BioMed Central 2014 2014-04-29 /pmc/articles/PMC4075243/ /pubmed/24779919 http://dx.doi.org/10.1186/ar4554 Text en Copyright © 2014 Li et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Li, Chun
Mu, Rong
Guo, Jianping
Wu, Xinyu
Tu, Xin
Liu, Xu
Hu, Fanlei
Guo, Shiwei
Zhu, Jiaxin
Xu, Huji
Li, Zhanguo
Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title_full Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title_fullStr Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title_full_unstemmed Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title_short Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis
title_sort genetic variant in il33 is associated with susceptibility to rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075243/
https://www.ncbi.nlm.nih.gov/pubmed/24779919
http://dx.doi.org/10.1186/ar4554
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