Wang Lina, Yang Bo, Zhou Shiyuan, Gao Huafang, Wang Fengyu, Zhou Jiping, Wang Haili, Wang Yanli
Peking Union Medical College Graduate School, Beijing 100000, China.
National Research Institute for Health and Family Planning 100000, Beijing, China.
J Thorac Dis. 2018 Jan;10(1):441-447. doi: 10.21037/jtd.2017.12.08.
Congenital heart disease (CHD), which involve congenital cardiovascular malformations that occur during an embryo stage, may be the result of a complex interaction between genetic factors and environmental factors. The homozygous 677 T/T MTHFR gene and potential factors have been associated with CHD. Our objective was to study associations between potential environmental risk factors and methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms in CHD.
A total of 346 children with CHD and 237 healthy children were recruited. Their parents were also enlisted in the study and interviewed face-to-face to identify potential environmental risk factors. The MTHFR genotype was analyzed by restriction fragment length polymorphism (RFLP). Interactions between environmental risk factors and MTHFR gene polymorphisms were evaluated by the relative excess risk due to interaction (RERI), the attributable proportion due to interaction (AP), and the synergy index (S).
There were significant differences in the occupational statuses of the mothers and their levels of drug exposure during gestation between the controls and the cases (P<0.05). These differences significantly increased offspring CHD risk (occupation: OR =5.45, 95% CI: 3.46-8.58; drug exposure: OR =4.91, 95% CI: 2.18-11.09). The frequency of the MTHFR gene 677 TT polymorphism in the mothers who had offspring with CHD was significantly different from that in the non-CHD controls (P<0.05). The frequency of this polymorphism also significantly differed between the children with CHD and the control group (P<0.05). An interaction was identified between the presence of the homozygous 677 TT genotype in the children and the mothers' occupational statuses (RERI =9.43, CI: 0.06-18.91).
A significant interaction was found between the homozygous 677 T/T MTHFR gene in children and the maternal occupational status and level of drug exposure during gestation. Avoiding or reducing the exposure of the risk factors mentioned above, strengthening pre-pregnancy checkups and guidance might help to reduce the risk of CHD.
先天性心脏病(CHD)涉及胚胎期发生的先天性心血管畸形,可能是遗传因素和环境因素复杂相互作用的结果。纯合子677 T/T MTHFR基因及潜在因素与先天性心脏病有关。我们的目的是研究先天性心脏病中潜在环境危险因素与亚甲基四氢叶酸还原酶(MTHFR)基因多态性之间的关联。
共招募了346名先天性心脏病患儿和237名健康儿童。他们的父母也参与了研究,并进行面对面访谈以确定潜在的环境危险因素。通过限制性片段长度多态性(RFLP)分析MTHFR基因型。通过交互作用的相对超额危险度(RERI)、交互作用归因比例(AP)和协同指数(S)评估环境危险因素与MTHFR基因多态性之间的相互作用。
对照组和病例组母亲的职业状况及其孕期药物暴露水平存在显著差异(P<0.05)。这些差异显著增加了后代患先天性心脏病的风险(职业:OR =5.45,95% CI:3.46 - 8.58;药物暴露:OR =4.91,95% CI:2.18 - 11.09)。患有先天性心脏病后代的母亲中MTHFR基因677 TT多态性的频率与非先天性心脏病对照组显著不同(P<0.05)。这种多态性的频率在先天性心脏病患儿和对照组之间也有显著差异(P<0.05)。在儿童中纯合子677 TT基因型的存在与母亲的职业状况之间存在相互作用(RERI =9.43,CI:0.06 - 18.91)。
在儿童中发现纯合子677 T/T MTHFR基因与母亲的职业状况及孕期药物暴露水平之间存在显著的相互作用。避免或减少上述危险因素的暴露,加强孕前检查和指导可能有助于降低先天性心脏病的风险。