Maternal late-pregnancy serum unmetabolized folic acid concentrations are not associated with infant allergic disease - A prospective cohort study

K. Best, T. Green, D. Sulistyoningrum, Thomas R Sullivan, S. Aufreiter, S. Prescott, M. Makrides, M. Skubisz, D. O’Connor, D. Palmer
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引用次数: 7

Abstract

Background: The increase in childhood allergic disease in recent decades has coincided with increased folic acid intakes during pregnancy. Circulating unmetabolized folic acid (UMFA) has been proposed as a biomarker of excessive folic acid intake. Objective: We aimed to determine if late-pregnancy serum UMFA and total folate concentrations were associated with allergic disease risk in the offspring at one year of age in a population at high risk of allergy. Methods: The cohort consisted of 561 mother-infant pairs from Western Australia. To be eligible the infant had a first-degree relative (mother, father or sibling) with a history of medically diagnosed allergic disease. Maternal serum was collected between 36 and 40 weeks of gestation. UMFA concentrations were measured by tandem mass spectrometry using stable isotope dilution, folate concentrations were determined using the microbiological method with standardized kits. Infant allergic disease outcomes of medically diagnosed eczema, steroid treated eczema, atopic eczema, IgE-mediated food allergy, allergen sensitization and medically diagnosed wheeze were assessed at 1 year of age. Results: Median (IQR) for UMFA and serum folate was 1.6 (0.6-4.7) and 53.2 (32.6-74.5) nmol/L, respectively. Of the infants, 34.6% had medically diagnosed eczema, 26.4% allergen sensitization and 14.9% had an IgE-mediated food allergy. In both adjusted and unadjusted models there was little evidence of association between UMFA or serum folate and any of the infant allergy outcomes. Conclusion: In this cohort of children at high risk for allergic disease there was no association between maternal UMFA or serum folate measured in late pregnancy and allergic disease outcomes at 1 year of age.
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孕妇妊娠晚期血清未代谢叶酸浓度与婴儿过敏性疾病无关——一项前瞻性队列研究
背景:近几十年来,儿童过敏性疾病的增加与怀孕期间叶酸摄入量的增加相吻合。循环未代谢叶酸(UMFA)已被提出作为过量叶酸摄入的生物标志物。目的:我们旨在确定在过敏高危人群中,妊娠后期血清UMFA和总叶酸浓度是否与1岁时子代过敏性疾病风险相关。方法:该队列由来自西澳大利亚州的561对母婴组成。婴儿有一级亲属(母亲、父亲或兄弟姐妹)有医学诊断的过敏性疾病史才符合条件。在妊娠36 ~ 40周期间采集母体血清。UMFA浓度采用稳定同位素稀释串联质谱法测定,叶酸浓度采用标准化试剂盒微生物学方法测定。在1岁时评估医学诊断湿疹、类固醇治疗湿疹、特应性湿疹、ige介导的食物过敏、过敏原致敏和医学诊断喘息的婴儿变应性疾病结局。结果:UMFA和血清叶酸的中位数(IQR)分别为1.6(0.6-4.7)和53.2 (32.6-74.5)nmol/L。在这些婴儿中,34.6%有医学诊断的湿疹,26.4%有过敏原致敏,14.9%有ige介导的食物过敏。在调整和未调整的模型中,几乎没有证据表明UMFA或血清叶酸与任何婴儿过敏结果之间存在关联。结论:在这组过敏性疾病高危儿童中,妊娠后期母体UMFA或血清叶酸与1岁时过敏性疾病结局无关联。
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