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白细胞介素1受体1基因多态性与儿童哮喘的关联

[Association between IL1R1 gene polymorphisms and childhood asthma].

作者信息

Liu Yan, Liu Sheng, Wu Hong-Hui, Zhang Xiang

机构信息

Department of Pediatrics, Xianning Central Hospital, Xianning, Hubei 437100, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2016 Mar;18(3):243-6. doi: 10.7499/j.issn.1008-8830.2016.03.011.

DOI:10.7499/j.issn.1008-8830.2016.03.011
PMID:26975823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7389989/
Abstract

OBJECTIVE

To investigate the association of two single-nucleotide polymorphisms (SNPs) in IL1R1 gene (rs1558641 and rs949963) with the susceptibility to asthma in children from Central China.

METHODS

A case-control study was performed in the asthma group and the control group, consisting of 208 children with asthma and 223 normal children from Central China, respectively. The genotypes of two SNPs in IL1R1 gene, rs1558641 and rs949963, were identified using polymerase chain reaction-restriction fragment length polymorphism. The serum level of IL1R1 was determined by enzyme-linked immunosorbent assay.

RESULTS

There were no significant differences in genotype and allele frequencies of rs1558641 between the asthma and control groups. In terms of rs949963, the frequencies of GG genotype and alleles were significantly higher in the asthma group than in the control group (P<0.05). The asthma group had a significantly higher serum level of IL1R1 than the control group (P=0.011). Moreover, the serum level of IL1R1 was significantly higher in patients with GG genotype than in those with AA or AG genotype for rs949963 (P=0.028).

CONCLUSIONS

IL1R1 SNP rs949963 is associated with the susceptibility to asthma in children from Central China and may increase the serum expression of IL1R1.

摘要

目的

探讨白细胞介素1受体1(IL1R1)基因中的两个单核苷酸多态性(SNP)(rs1558641和rs949963)与中国中部地区儿童哮喘易感性的关系。

方法

进行病例对照研究,哮喘组和对照组分别由来自中国中部地区的208例哮喘儿童和223例正常儿童组成。采用聚合酶链反应-限制性片段长度多态性方法鉴定IL1R1基因中两个SNP(rs1558641和rs949963)的基因型。通过酶联免疫吸附测定法测定血清IL1R1水平。

结果

哮喘组和对照组之间rs1558641的基因型和等位基因频率无显著差异。就rs949963而言,哮喘组中GG基因型和等位基因的频率显著高于对照组(P<0.05)。哮喘组的血清IL1R1水平显著高于对照组(P=0.011)。此外,rs949963的GG基因型患者的血清IL1R1水平显著高于AA或AG基因型患者(P=0.028)。

结论

IL1R1 SNP rs949963与中国中部地区儿童哮喘易感性相关,可能增加IL1R1的血清表达。

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Chemosphere. 2016 Feb;144:168-75. doi: 10.1016/j.chemosphere.2015.08.084. Epub 2015 Sep 9.
2
IL-1R1 is expressed on both Helios(+) and Helios(-) FoxP3(+) CD4(+) T cells in the rheumatic joint.白细胞介素-1受体1(IL-1R1)在风湿性关节中的Helios(+)和Helios(-) FoxP3(+) CD4(+) T细胞上均有表达。
Clin Exp Immunol. 2015 Oct;182(1):90-100. doi: 10.1111/cei.12668. Epub 2015 Jul 30.
3
[Association between CHI3L1 SNPs and susceptibility to childhood asthma].几丁质酶3样蛋白1基因单核苷酸多态性与儿童哮喘易感性的关联
Zhongguo Dang Dai Er Ke Za Zhi. 2015 Feb;17(2):144-8.
4
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Infect Immun. 2014 May;82(5):2106-14. doi: 10.1128/IAI.01579-13. Epub 2014 Mar 10.
5
The structural pathway of interleukin 1 (IL-1) initiated signaling reveals mechanisms of oncogenic mutations and SNPs in inflammation and cancer.白细胞介素1(IL-1)启动信号的结构途径揭示了炎症和癌症中致癌突变和单核苷酸多态性的机制。
PLoS Comput Biol. 2014 Feb 13;10(2):e1003470. doi: 10.1371/journal.pcbi.1003470. eCollection 2014 Feb.
6
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7
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.全基因组关联研究确定 CDHR3 是儿童期早发性哮喘严重恶化的易感基因位点。
Nat Genet. 2014 Jan;46(1):51-5. doi: 10.1038/ng.2830. Epub 2013 Nov 17.
8
Associations and interactions of genetic polymorphisms in innate immunity genes with early viral infections and susceptibility to asthma and asthma-related phenotypes.固有免疫基因遗传多态性与早期病毒感染及易感性哮喘和哮喘相关表型的关联和相互作用。
J Allergy Clin Immunol. 2012 Dec;130(6):1284-93. doi: 10.1016/j.jaci.2012.07.051. Epub 2012 Oct 9.
9
The single nucleotide polymorphism CRTh2 rs533116 is associated with allergic asthma and increased expression of CRTh2.单一核苷酸多态性 CRTh2 rs533116 与过敏性哮喘和 CRTh2 表达增加有关。
Allergy. 2012 Nov;67(11):1357-64. doi: 10.1111/all.12003. Epub 2012 Sep 5.
10
Phosphatidylinositol 3-kinase in interleukin 1 signaling. Physical interaction with the interleukin 1 receptor and requirement in NFkappaB and AP-1 activation.白细胞介素1信号传导中的磷脂酰肌醇3激酶。与白细胞介素1受体的物理相互作用以及对核因子κB和活化蛋白-1激活的需求。
J Biol Chem. 1997 Nov 14;272(46):29167-73. doi: 10.1074/jbc.272.46.29167.