Women and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, Australia.
Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
J Nutr. 2021 Jun 1;151(6):1553-1560. doi: 10.1093/jn/nxab040.
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.
We aimed to determine if late-pregnancy serum UMFA and total folate concentrations were associated with allergic disease risk in the offspring at 1 y of age in a population at high risk of allergy.
The cohort consisted of 561 mother-infant pairs from Western Australia. To be eligible the infant had to have a first-degree relative (mother, father, or sibling) with a history of medically diagnosed allergic disease. Maternal venous blood was collected between 36 and 40 wk of gestation. Serum UMFA was measured by LC-tandem MS. Serum total folate was determined using a microbiological method with chloramphenicol-resistant Lactobacillus rhamnosus as the test organism, and was collected between 36 and 40 wk of gestation. UMFA concentrations were measured by tandem MS 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 y of age.
Median (IQR) concentrations for UMFA and serum folate were 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.
In this cohort of children at high risk of allergic disease there was no association between maternal UMFA or serum folate concentrations measured in late pregnancy and allergic disease outcomes at 1 y of age.
近几十年来,儿童过敏性疾病的发病率有所增加,而孕妇叶酸摄入量也随之增加。循环未代谢叶酸(UMFA)已被提出作为叶酸摄入过量的生物标志物。
我们旨在确定在高过敏风险人群中,妊娠晚期血清 UMFA 和总叶酸浓度与 1 岁婴儿过敏疾病风险之间的关系。
该队列包括来自西澳大利亚的 561 对母婴。婴儿的一级亲属(母亲、父亲或兄弟姐妹)必须有经医学诊断的过敏病史才有资格入组。在妊娠 36 至 40 周时采集母亲静脉血。采用 LC-串联质谱法测量血清 UMFA。采用微生物法测定血清总叶酸,以氯霉素抗性鼠李糖乳杆菌作为检测生物,采集时间为妊娠 36 至 40 周。采用串联质谱法用稳定同位素稀释法测量 UMFA 浓度;采用微生物法用标准化试剂盒测定叶酸浓度。在 1 岁时评估婴儿过敏疾病的结果,包括经医学诊断的湿疹、皮质类固醇治疗的湿疹、特应性皮炎、IgE 介导的食物过敏、过敏原致敏和经医学诊断的喘息。
UMFA 和血清叶酸的中位数(IQR)浓度分别为 1.6(0.6-4.7)和 53.2(32.6-74.5)nmol/L。在这些婴儿中,34.6%有经医学诊断的湿疹,26.4%有过敏原致敏,14.9%有 IgE 介导的食物过敏。在调整和未调整模型中,UMFA 或血清叶酸与婴儿任何过敏结果之间几乎没有关联。
在该高过敏风险的儿童队列中,妊娠晚期测量的母体 UMFA 或血清叶酸浓度与 1 岁时的过敏疾病结果之间没有关联。