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2
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Int Arch Allergy Immunol. 2011;154(4):328-35. doi: 10.1159/000321825. Epub 2010 Oct 25.
3
A multi-centre study of candidate genes for wheeze and allergy: the International Study of Asthma and Allergies in Childhood Phase 2.多中心候选基因研究喘息和过敏:儿童哮喘和过敏国际研究第二阶段。
Clin Exp Allergy. 2009 Dec;39(12):1875-88. doi: 10.1111/j.1365-2222.2009.03364.x.
4
Prevalence of atopic dermatitis in Japanese adults and community validation of the U.K. diagnostic criteria.日本成年人特应性皮炎的患病率及英国诊断标准的社区验证
J Dermatol Sci. 2009 Aug;55(2):140-1. doi: 10.1016/j.jdermsci.2009.04.004. Epub 2009 May 8.
5
Contribution of functional variation in the IL13 gene to allergy, hay fever and asthma in the NSHD longitudinal 1946 birth cohort.IL13基因功能变异对1946年出生的全国儿童发育研究纵向队列中过敏、花粉热和哮喘的影响。
Allergy. 2009 Aug;64(8):1172-8. doi: 10.1111/j.1398-9995.2009.01988.x. Epub 2009 Feb 27.
6
Polymorphisms in the interleukin 13 and GATA binding protein 3 genes and the development of eczema during childhood.白细胞介素13和GATA结合蛋白3基因多态性与儿童期湿疹的发生发展
Br J Dermatol. 2008 Jun;158(6):1315-22. doi: 10.1111/j.1365-2133.2008.08565.x. Epub 2008 Apr 10.
7
Th2 cell-selective enhancement of human IL13 transcription by IL13-1112C>T, a polymorphism associated with allergic inflammation.IL13-1112C>T(一种与过敏性炎症相关的多态性)对人IL13转录的Th2细胞选择性增强作用。
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8
No association of cytokine gene polymorphisms in Chinese patients with atopic dermatitis.中国特应性皮炎患者细胞因子基因多态性无相关性。
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9
Parental tobacco smoking is associated with augmented IL-13 secretion in children with allergic asthma.父母吸烟与过敏性哮喘儿童白细胞介素-13分泌增加有关。
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Calculating measures of biological interaction.计算生物相互作用的指标。
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白细胞介素 13 基因多态性、吸烟与女性特应性皮炎:日本一项病例对照研究。

IL13 genetic polymorphisms, smoking, and eczema in women: a case-control study in Japan.

机构信息

Department of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

出版信息

BMC Med Genet. 2011 Oct 21;12:142. doi: 10.1186/1471-2350-12-142.

DOI:10.1186/1471-2350-12-142
PMID:22013915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3206833/
Abstract

BACKGROUND

Several genetic association studies have examined the relationships between single nucleotide polymorphisms (SNPs) in the IL13 gene and eczema, and have provided contradictory results. We investigated the relationship between the IL13 SNPs rs1800925 and rs20541 and the risk of eczema in Japanese young adult women.

METHODS

Included were 188 cases who met the criteria of the International Study of Asthma and Allergies in Childhood (ISAAC) for eczema. Control subjects were 1,082 women without eczema according to the ISAAC criteria, who had not been diagnosed with atopic eczema by a doctor and who had no current asthma as defined by the European Community Respiratory Health Survey criteria. Adjustment was made for age, region of residence, number of children, smoking, and education.

RESULTS

The minor TT genotype of SNP rs1800925 was significantly associated with an increased risk of eczema in the co-dominant model: the adjusted odds ratio was 2.19 (95% confidence interval: 1.03-4.67). SNP rs20541 was not related to eczema. None of the haplotypes were significantly associated with eczema. Compared with women with the CC or CT genotype of SNP rs1800925 who had never smoked, those with the TT genotype who had ever smoked had a 2.85-fold increased risk of eczema, though the adjusted odds ratio was not statistically significant, and neither multiplicative nor additive interaction was statistically significant.

CONCLUSIONS

Our findings suggest that the IL13 SNP rs1800925 is significantly associated with eczema in Japanese young adult women. We could not find evidence for an interaction between SNP rs1800925 and smoking with regard to eczema.

摘要

背景

多项单核苷酸多态性(SNP)与白细胞介素 13 基因(IL13)和特应性皮炎之间关系的遗传关联研究提供了相互矛盾的结果。我们调查了白细胞介素 13 基因 SNP rs1800925 和 rs20541 与日本年轻成年女性特应性皮炎风险之间的关系。

方法

纳入了符合儿童国际哮喘和过敏研究(ISAAC)特应性皮炎标准的 188 例病例。对照者为根据 ISAAC 标准无特应性皮炎、未经医生诊断为特应性皮炎且欧洲社区呼吸健康调查标准无当前哮喘的 1082 名女性。调整了年龄、居住地区、子女数量、吸烟和教育程度。

结果

SNP rs1800925 的次要 TT 基因型在共显性模型中与特应性皮炎风险增加显著相关:调整后的比值比为 2.19(95%置信区间:1.03-4.67)。SNP rs20541 与特应性皮炎无关。没有任何单倍型与特应性皮炎显著相关。与从未吸烟的 SNP rs1800925 中 CC 或 CT 基因型的女性相比,曾经吸烟的 TT 基因型女性特应性皮炎的风险增加了 2.85 倍,但调整后的比值比无统计学意义,且不存在乘法或加法交互作用。

结论

我们的研究结果表明,IL13 SNP rs1800925 与日本年轻成年女性特应性皮炎显著相关。我们没有发现 SNP rs1800925 与吸烟之间对特应性皮炎存在交互作用的证据。