Pei Lijun, Zhu Huiping, Ye Rongwei, Wu Jilei, Liu Jianmeng, Ren Aiguo, Li Zhiwen, Zheng Xiaoying
Institute of Population Research, Peking University, Beijing, China.
Birth Defects Res A Clin Mol Teratol. 2015 Jan;103(1):3-11. doi: 10.1002/bdra.23257. Epub 2014 Jun 11.
Many studies have indicated that the reduced folate carrier gene (SLC19A1) is associated with an increased risk of neural tube defects (NTDs). However, the interaction between the SLC19A1 gene variant and maternal fever exposure and NTD risk remains unknown. The aim of this study was to investigate whether the risk for NTDs was influenced by the interactions between the SLC19A1 (rs1051266) variant and maternal first trimester fever.
We investigated the potential interaction between maternal first trimester fever and maternal or offspring SLC19A1 polymorphism through a population-based case-control study. One hundred and four nuclear families with NTDs and 100 control families with nonmal newborns were included in the study. SLC19A1 polymorphism was determined using polymerase chain reaction-restricted fragment length polymorphism.
Mothers who had the GG/GA genotype and first trimester fever had an elevated risk of NTDs (adjusted odds ratio, 11.73; 95% confidence interval, 3.02-45.58) as compared to absence of maternal first trimester fever and AA genotype after adjusting for maternal education, paternal education, and age, and had a significant interactive coefficient (γ = 3.17) between maternal GG/GA genotype and first trimester fever. However, there was no interaction between offspring's GG/GA genotype and maternal first trimester fever (the interactive coefficient γ = 0.97) after adjusting for confounding factors.
Our findings suggested that the risk of NTDs was potentially influenced by a gene-environment interaction between maternal SLC19A1 rs1051266 GG/GA genotype and first trimester fever. Maternal GG/GA genotype may strengthen the effect of maternal fever exposure on NTD risk in this Chinese population.
许多研究表明,还原型叶酸载体基因(SLC19A1)与神经管缺陷(NTDs)风险增加有关。然而,SLC19A1基因变异与孕期母体发热暴露及NTDs风险之间的相互作用仍不清楚。本研究的目的是调查SLC19A1(rs1051266)变异与孕早期母体发热之间的相互作用是否会影响NTDs风险。
我们通过一项基于人群的病例对照研究,调查了孕早期母体发热与母体或子代SLC19A1多态性之间的潜在相互作用。本研究纳入了104个有神经管缺陷的核心家庭和100个有正常新生儿的对照家庭。采用聚合酶链反应-限制性片段长度多态性方法测定SLC19A1多态性。
在调整了母体教育程度、父亲教育程度和年龄后,具有GG/GA基因型且孕早期发热的母亲发生神经管缺陷的风险升高(调整后的优势比为11.73;95%置信区间为3.02-45.58),与孕早期无发热且为AA基因型的母亲相比,母体GG/GA基因型与孕早期发热之间存在显著的交互系数(γ=3.17)。然而,在调整混杂因素后,子代的GG/GA基因型与孕早期母体发热之间没有相互作用(交互系数γ=0.97)。
我们的研究结果表明,母体SLC19A1 rs1051266 GG/GA基因型与孕早期发热之间的基因-环境相互作用可能会影响神经管缺陷的风险。在这个中国人群中,母体GG/GA基因型可能会增强母体发热暴露对神经管缺陷风险的影响。