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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >IgE in unselected like-sexed monozygotic and dizygotic twins at birth and at 6 to 9 years of age: high but dissimilar genetic influence on IgE levels.
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IgE in unselected like-sexed monozygotic and dizygotic twins at birth and at 6 to 9 years of age: high but dissimilar genetic influence on IgE levels.

机译:未选择的同性双卵和双卵双生双胞胎在出生时和6至9岁时的IgE:对IgE水平的遗传影响高但相似。

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BACKGROUND: IgE is a major determinant of allergic disease. Twin analysis of serum levels of IgE has been carried out previously in children and adults with heritability estimates of 30% to 70% on the basis of ANOVA. OBJECTIVE: This study included the analysis of serum IgE in a population of 126 twins, 27 monozygotic pairs and 36 dizygotic pairs, studied at birth (cord blood [CB] IgE) and consecutively at the age of 6 to 9 years of age (serum IgE). METHODS: IgE was determined by means of RIA. ANOVA, correlation analysis, and structural equation modeling by maximal likelihood analysis was used for genetic analysis. RESULTS: Structural equation modeling by maximal likelihood analysis showed the best-fitting model to be the AE model (A for additive genetic variance and E for environmental variance) both at birth and later in childhood. The estimated heritability was 0.92 (95% CI, 0.84-0.95) for CB IgE and 0.78 (95% CI, 0.60-0.87) for serum IgE. The correlation between CB IgE and serum IgE was 0.04. CONCLUSIONS: The study demonstrated a higher genetic dependency of serum IgE than previously recognized. The low correlation between the IgE levels at birth and later in childhood suggested that different effector mechanisms may be operating at different ages.
机译:背景:IgE是过敏性疾病的主要决定因素。先前已在儿童和成人中对IgE血清水平进行了双重分析,根据ANOVA,遗传力估计为30%至70%。目的:本研究包括分析出生时(脐血[CB] IgE)和6至9岁年龄(血清)的126对双胞胎,27对单卵对和36对双卵对人群的血清IgE。 IgE)。方法:通过RIA测定IgE。方差分析,相关性分析和最大似然分析的结构方程模型用于遗传分析。结果:通过最大似然分析进行的结构方程建模表明,最合适的模型是出生时和儿童期的AE模型(A用于加性遗传变异,E用于环境变异)。 CB IgE的估计遗传度为0.92(95%CI,0.84-0.95),血清IgE的估计遗传度为0.78(95%CI,0.60-0.87)。 CB IgE与血清IgE之间的相关性为0.04。结论:该研究表明血清IgE的遗传依赖性高于以前的认识。出生时和儿童期后期的IgE水平之间的相关性较低,表明不同的效应器机制可能在不同的年龄起作用。

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