儿童特应性哮喘:与IL-4受体α基因多态性呈正相关,但与IL-4启动子或Fc epsilon受体I β基因多态性无关。

A Takabayashi, K Ihara, Y Sasaki, Y Suzuki, S Nishima, K Izuhara, N Hamasaki, T Hara
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引用次数: 49

摘要

我们检查了三个代表性的特应性候选基因(Fc ε受体I β, IL-4和IL-4受体α)对特应性哮喘发展的相对贡献。在日本九州北部地区的100例特应性哮喘患者和100例非特应性对照中,研究了IL-4受体α的Ile50Val和Gln551Arg、IL-4启动子的-590C/T和Fc epsilon受体I β的Glu237Gly这3个候选基因的4个多态性。在3个候选基因的4个多态性中,IL-4受体α链基因的Ile50等位基因与特应性哮喘患者相关(p = 0.044),特别是在2岁或更早发病的患者中(p = 0.034)和中重度特应性哮喘患者中(p = 0.044)。031)。IL-4受体α的Gln551Arg、IL-4启动子的-590C/T和Fc epsilon受体I β的Glu237Gly与特应性哮喘无相关性。IL-4受体α链基因Ile50Val和Gln551Arg多态性在患者和非特应性对照中均存在轻微的连锁不平衡。在具有一定遗传背景的地区鉴定额外的特应性基因对于遗传诊断和建立特应性哮喘的新治疗方式至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Childhood atopic asthma: positive association with a polymorphism of IL-4 receptor alpha gene but not with that of IL-4 promoter or Fc epsilon receptor I beta gene.

We examined the relative contributions of three representative candidate genes for atopy (Fc epsilon receptor I beta, IL-4, and IL-4 receptor alpha) to the development of atopic asthma. Four polymorphisms of the three candidate genes including Ile50Val and Gln551Arg of IL-4 receptor alpha, -590C/T of IL-4 promoter and Glu237Gly of Fc epsilon receptor I beta were studied in 100 patients with atopic asthma and 100 nonatopic controls in the northern Kyushu area in Japan. Among the four polymorphisms of the three candidate genes, the Ile50 allele of the IL-4 receptor alpha chain gene demonstrated an association with atopic asthma subjects (p = 0.044), especially in patients with onset at 2 years of age or earlier (p = 0.034) and in patients with moderate to severe atopic asthma (p = 0. 031). Gln551Arg of IL-4 receptor alpha, -590C/T of IL-4 promoter and Glu237Gly of Fc epsilon receptor I beta showed no association with atopic asthma. A slight linkage disequilibrium between Ile50Val and Gln551Arg polymorphisms of the IL-4 receptor alpha chain gene was observed in both patients and nonatopic controls. The identification of additional atopy genes in areas with a certain genetic background is essential for genetic diagnosis and to establish new therapeutic modalities for atopic asthma.

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