Granell R, Heron J, Lewis S, Davey Smith G, Sterne J A C, Henderson J
ALSPAC, Department of Social Medicine, University of Bristol, Bristol, UK.
Clin Exp Allergy. 2008 Feb;38(2):320-8. doi: 10.1111/j.1365-2222.2007.02902.x. Epub 2007 Dec 7.
A recent study suggested a link between folate metabolism and atopy, based on a positive association between a common polymorphism of the methylenetetrahydrofolate reductase (MTHFR) gene and allergic sensitization in Danish adults.
We investigated the associations between MTHFR C677T and allergy or atopy in a large, population-based birth cohort of children and their mothers, the Avon Longitudinal Study of Parents and Children (ALSPAC). We also looked for evidence of a pre-natal effect of maternal folate metabolism on subsequent atopic disease in the offspring.
Mothers were recruited in pregnancy and the children followed from birth. Atopy in the child was assessed at 7-8 years of age by skin prick tests to common allergens. Asthma was defined as a physician diagnosis and current symptoms at 71/2 years of age. Asthma and allergy status of the mothers were obtained from self-completion questionnaires.
Data on MTHFR C677T genotype and allergy were available for 5364 children and on allergy and/or asthma for 7356 mothers. In children, the prevalence of atopy was 20.0% and asthma 10.0% whereas in mothers, the prevalence of self-reported allergy was 42.7% and asthma 11.5%. Atopy in the child was associated with male gender (P<0.001), less tobacco smoke exposure and higher maternal education. MTHFR C677T genotype was not associated with social factors or dietary folate intake. We found no evidence of associations between the MTHFR C677T variant allele and atopy, allergy or asthma in mothers or children. There was no evidence to support an effect of maternal MTHFR C677T genotype on atopy in the offspring.
The results of this study do not support the hypothesis that impaired folate metabolism is associated with allergy in adults or children in this population.
最近一项研究表明,基于丹麦成年人中亚甲基四氢叶酸还原酶(MTHFR)基因常见多态性与过敏致敏之间的正相关关系,叶酸代谢与特应性之间存在联系。
我们在一个以人群为基础的大型儿童及其母亲出生队列——阿冯父母与儿童纵向研究(ALSPAC)中,调查了MTHFR C677T与过敏或特应性之间的关联。我们还寻找证据证明母亲叶酸代谢对后代随后发生的特应性疾病有产前影响。
母亲在孕期被招募,孩子从出生开始随访。孩子7至8岁时通过对常见变应原进行皮肤点刺试验来评估特应性。哮喘定义为医生诊断且在7.5岁时有当前症状。母亲的哮喘和过敏状态通过自我填写问卷获得。
有5364名儿童的MTHFR C677T基因型和过敏数据,以及7356名母亲的过敏和/或哮喘数据。在儿童中,特应性患病率为20.0%,哮喘患病率为10.0%;而在母亲中,自我报告的过敏患病率为42.7%,哮喘患病率为11.5%。儿童特应性与男性性别(P<0.001)、较少接触烟草烟雾以及母亲较高的教育程度相关。MTHFR C677T基因型与社会因素或膳食叶酸摄入量无关。我们没有发现MTHFR C677T变异等位基因与母亲或儿童的特应性、过敏或哮喘之间存在关联的证据。没有证据支持母亲MTHFR C677T基因型对后代特应性有影响。
本研究结果不支持叶酸代谢受损与该人群中成人或儿童过敏相关的假设。