首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Interleukin-1 receptor-like 1 polymorphisms are associated with serum IL1RL1-a, eosinophils, and asthma in childhood.
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Interleukin-1 receptor-like 1 polymorphisms are associated with serum IL1RL1-a, eosinophils, and asthma in childhood.

机译:白细胞介素-1受体样1多态性与儿童血清IL1RL1-a,嗜酸性粒细胞和哮喘有关。

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BACKGROUND: IL-1 receptor-like 1 (IL1RL1) is a membrane receptor involved in T(H)2 inflammatory responses and eosinophilia. Single nucleotide polymorphisms (SNPs) in IL1RL1 have been associated with blood eosinophil counts in a genome-wide association study and with asthma in family-based and case-control studies. OBJECTIVE: We assessed in the prospective birth cohort Prevention and Incidence of Asthma and Mite Allergy (PIAMA) whether IL1RL1 SNPs associate with levels of its soluble transcript IL1RL1 (IL1RL1-a) in serum, blood eosinophil counts, and asthma prevalence from birth to age 8 years, and whether IL1RL1-a serum levels associate with blood eosinophil counts. METHODS: Fifteen IL1RL1 SNPs were genotyped. Serum IL1RL1-a levels were measured in 2 independent subsets within PIAMA, at 4 and 8 years. Blood eosinophil counts were measured in 4-year-old children. RESULTS: In 2 independent subsets of children, 13 of 15 SNPs were associated with serum IL1RL1-a levels at ages 4 and 8 years with a consistent direction of effect for each allele. Rs11685480 allele A and rs1420102 allele A were significantly associated with lower numbers of blood eosinophils. In the total cohort, rs1041973 allele A was associated with a decreased risk of developing asthma (odds ratio, 0.70; 95% CI, 0.54-0.90). Rs1420101, recently identified in a genome-wide association study in the Icelandic population, was not associated with asthma in this study. IL1RL1-a levels were not associated with eosinophil counts. CONCLUSION: We demonstrate that IL1RL1 polymorphisms are associated with serum IL1RL1-a, blood eosinophils, and asthma in childhood.
机译:背景:IL-1受体样1(IL1RL1)是参与T(H)2炎症反应和嗜酸性粒细胞增多的膜受体。在全基因组关联研究中,IL1RL1中的单核苷酸多态性(SNP)与血液嗜酸性粒细胞计数有关,在基于家庭和病例对照研究中与哮喘有关。目的:我们在前瞻性出生队列中对哮喘和螨虫过敏的预防和发生率(PIAMA)进行了评估,从出生到年龄,IL1RL1 SNPs是否与血清,血液嗜酸性粒细胞计数和哮喘患病率的可溶性转录因子IL1RL1(IL1RL1-a)水平相关8年,以及IL1RL1-a血清水平是否与血液嗜酸性粒细胞计数相关。方法:对15个IL1RL1 SNP进行基因分型。在4年和8年时,在PIAMA中的2个独立亚组中测量了血清IL1RL1-a水平。测量了4岁儿童的嗜酸性粒细胞计数。结果:在2个独立的儿童亚组中,15个SNP中的13个与4岁和8岁时的血清IL1RL1-a水平相关,每​​个等位基因的作用方向一致。 Rs11685480等位基因A和rs1420102等位基因A与较少数量的血液嗜酸性粒细胞显着相关。在整个队列中,rs1041973等位基因A与患哮喘的风险降低相关(比值比为0.70; 95%CI为0.54-0.90)。最近在冰岛人群的全基因组关联研究中确定的Rs1420101与哮喘没有关联。 IL1RL1-a水平与嗜酸性粒细胞计数无关。结论:我们证明IL1RL1多态性与儿童血清IL1RL1-a,血液嗜酸性粒细胞和哮喘有关。

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