David Hide Asthma and Allergy Research Centre, Isle of Wight, United Kingdom.
J Allergy Clin Immunol. 2012 Aug;130(2):427-34.e6. doi: 10.1016/j.jaci.2012.03.042. Epub 2012 May 18.
The parent-of-origin effect is important in understanding the genetic basis of childhood allergic diseases and improving our ability to identify high-risk children.
We sought to investigate the parent-of-origin effect in childhood allergic diseases.
The Isle of Wight Birth Cohort (n= 1456) has been examined at 1, 2, 4, 10, and 18 years of age. Information on the prevalence of asthma, eczema, rhinitis, and environmental factors was obtained by using validated questionnaires. Skin prick tests were carried out at ages 4, 10, and 18 years, and total IgE measurement was carried out at 10 and 18 years. Parental history of allergic disease was assessed soon after the birth of the child, when maternal IgE levels were also measured. Prevalence ratios (PRs) and their 95% CIs were estimated, applying log-linear models adjusted for confounding variables.
When stratified for sex of the child, maternal asthma was associated with asthma in girls (PR, 1.91; 95% CI, 1.34-2.72; P= .0003) but not in boys (PR, 1.29; 95% CI, 0.85-1.96; P= .23), whereas paternal asthma was associated with asthma in boys (PR, 1.99; 95% CI, 1.42-2.79; P< .0001) but not in girls (PR, 1.03; 95% CI, 0.59-1.80; P= .92). Maternal eczema increased the risk of eczema in girls (PR, 1.92; 95% CI, 1.37-2.68; P= .0001) only, whereas paternal eczema did the same for boys (PR, 2.07; 95% CI, 1.32-3.25; P = .002). Similar trends were observed when the effect of maternal and paternal allergic disease was assessed for childhood atopy and when maternal total IgE levels were related to total IgE levels in children at ages 10 and 18 years.
The current study indicates a sex-dependent association of parental allergic conditions with childhood allergies, with maternal allergy increasing the risk in girls and paternal allergy increasing the risk in boys. This has implications for childhood allergy prediction and prevention.
亲源性效应对于理解儿童过敏性疾病的遗传基础以及提高我们识别高危儿童的能力非常重要。
我们旨在研究儿童过敏性疾病中的亲源性效应。
对 Isle of Wight 出生队列(n=1456)在 1、2、4、10 和 18 岁时进行了检测。通过使用经过验证的调查问卷获得哮喘、湿疹、鼻炎和环境因素的患病率信息。在 4、10 和 18 岁时进行皮肤点刺试验,在 10 和 18 岁时进行总 IgE 测量。在孩子出生后不久评估父母的过敏病史,同时测量母亲的 IgE 水平。应用调整混杂因素的对数线性模型估计患病率比(PR)及其 95%置信区间(CI)。
按孩子的性别分层时,母亲哮喘与女孩哮喘相关(PR,1.91;95%CI,1.34-2.72;P=0.0003),但与男孩哮喘无关(PR,1.29;95%CI,0.85-1.96;P=0.23),而父亲哮喘与男孩哮喘相关(PR,1.99;95%CI,1.42-2.79;P<0.0001),但与女孩哮喘无关(PR,1.03;95%CI,0.59-1.80;P=0.92)。母亲湿疹增加了女孩患湿疹的风险(PR,1.92;95%CI,1.37-2.68;P=0.0001),而父亲湿疹则增加了男孩患湿疹的风险(PR,2.07;95%CI,1.32-3.25;P=0.002)。当评估母亲和父亲过敏疾病对儿童特应性的影响,以及当母亲总 IgE 水平与 10 岁和 18 岁儿童的总 IgE 水平相关时,也观察到了类似的趋势。
本研究表明,父母过敏状况与儿童过敏之间存在性别依赖性关联,母亲过敏会增加女孩的风险,而父亲过敏会增加男孩的风险。这对儿童过敏的预测和预防具有重要意义。