Liu Xin, Beaty Terri H, Deindl Philipp, Huang Shau-Ku, Lau Susanne, Sommerfeld Christine, Fallin M Daniele, Kao W H Linda, Wahn Ulrich, Nickel Renate
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
J Allergy Clin Immunol. 2003 Aug;112(2):382-8. doi: 10.1067/mai.2003.1635.
Increased total serum IgE levels are a common characteristic of atopic disorders. Six potentially functional variants, including C-590T in the IL4 gene, C-1055T and Arg130Gln in the IL13 gene, and Ile50Val, Ser478Pro, and Gln551Arg in the IL4RA gene, have been evaluated for their involvement in the control of total serum IgE levels and related atopic disorders, but the results of these studies have been inconsistent.
We examined whether these 6 variants had genotypic effects on total serum IgE levels in 823 unrelated German children from a large infant cohort, the German Multicenter Atopy Study.
Marginal effect models were used for the analyses of the repeated IgE measurements. Weighted linear regression and family-based tests of association were performed to minimize the possibility of spurious effects caused by selection bias or confounding on the basis of ethnic background.
There are significant associations between increased total serum IgE levels and 2 variants in the IL13 gene (P <.005 and.0002 for Arg130Gln and C-1055T, respectively). These genetic effects are unlikely to be due to solely linkage disequilibrium between 2 polymorphisms, population stratification, or nonrepresentative samples. In addition, exposure to maternal smoking appears to modify the above effects on total serum IgE levels. However, no statistical association was observed between this quantitative phenotype and the other 4 variants examined.
These findings suggest that variants C-1055T and Arg130Gln of the IL13 gene might play an important role on total serum IgE production in this study population.
血清总IgE水平升高是特应性疾病的常见特征。已对6个潜在的功能性变体进行评估,以确定它们是否参与血清总IgE水平的调控及相关特应性疾病,这些变体包括白细胞介素4(IL4)基因中的C-590T、白细胞介素13(IL13)基因中的C-1055T和精氨酸130谷氨酰胺(Arg130Gln),以及白细胞介素4受体A(IL4RA)基因中的异亮氨酸50缬氨酸(Ile50Val)、丝氨酸478脯氨酸(Ser478Pro)和谷氨酰胺551精氨酸(Gln551Arg),但这些研究结果并不一致。
我们在来自大型婴儿队列(德国多中心特应性研究)的823名无亲缘关系的德国儿童中,研究这6个变体对血清总IgE水平是否具有基因型效应。
采用边际效应模型分析重复的IgE测量值。进行加权线性回归和基于家系的关联检验,以尽量减少因选择偏倚或基于种族背景的混杂因素导致的虚假效应。
血清总IgE水平升高与IL13基因中的2个变体之间存在显著关联(Arg130Gln和C-1055T分别为P <.005和.0002)。这些遗传效应不太可能仅仅归因于2个多态性之间的连锁不平衡、群体分层或非代表性样本。此外,母亲吸烟似乎会改变上述对血清总IgE水平的影响。然而,在这种定量表型与其他4个检测变体之间未观察到统计学关联。
这些发现表明,在本研究人群中,IL13基因的C-1055T和Arg130Gln变体可能在血清总IgE产生中起重要作用。