Department of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.
PLoS One. 2013 Nov 5;8(11):e78462. doi: 10.1371/journal.pone.0078462. eCollection 2013.
Folate deficiency is implicated in the causation of neural tube defects (NTDs). The preventive effect of periconceptional folic acid supplement use is partially explained by the treatment of a deranged folate-dependent one carbon metabolism, which provides methyl groups for DNA-methylation as an epigenetic mechanism. Here, we hypothesize that variations in DNA-methylation of genes implicated in the development of NTDs and embryonic growth are part of the underlying mechanism. In 48 children with a neural tube defect and 62 controls from a Dutch case-control study and 34 children with a neural tube defect and 78 controls from a Texan case-control study, we measured the DNA-methylation levels of imprinted candidate genes (IGF2-DMR, H19, KCNQ1OT1) and non-imprinted genes (the LEKR/CCNL gene region associated with birth weight, and MTHFR and VANGL1 associated with NTD). We used the MassARRAY EpiTYPER assay from Sequenom for the assessment of DNA-methylation. Linear mixed model analysis was used to estimate associations between DNA-methylation levels of the genes and a neural tube defect. In the Dutch study group, but not in the Texan study group we found a significant association between the risk of having an NTD and DNA methylation levels of MTHFR (absolute decrease in methylation of -0.33% in cases, P-value = 0.001), and LEKR/CCNL (absolute increase in methylation: 1.36% in cases, P-value = 0.048), and a borderline significant association for VANGL (absolute increase in methylation: 0.17% in cases, P-value = 0.063). Only the association between MTHFR and NTD-risk remained significant after multiple testing correction. The associations in the Dutch study were not replicated in the Texan study. We conclude that the associations between NTDs and the methylation of the MTHFR gene, and maybe VANGL and LEKKR/CNNL, are in line with previous studies showing polymorphisms in the same genes in association with NTDs and embryonic development, respectively.
叶酸缺乏与神经管缺陷 (NTDs) 的发生有关。围孕期叶酸补充的预防作用部分可以通过纠正紊乱的叶酸依赖的一碳代谢来解释,该代谢为 DNA 甲基化提供甲基基团,作为一种表观遗传机制。在这里,我们假设与 NTD 发育和胚胎生长相关的基因的 DNA 甲基化变异是潜在机制的一部分。在一项来自荷兰病例对照研究的 48 名神经管缺陷患儿和 62 名对照者,以及一项来自德克萨斯州病例对照研究的 34 名神经管缺陷患儿和 78 名对照者中,我们测量了印迹候选基因(IGF2-DMR、H19、KCNQ1OT1)和非印迹基因(与出生体重相关的 LEKR/CCNL 基因区域,以及与 NTD 相关的 MTHFR 和 VANGL1)的 DNA 甲基化水平。我们使用 Sequenom 的 MassARRAY EpiTYPER 测定法进行 DNA 甲基化评估。线性混合模型分析用于估计基因的 DNA 甲基化水平与神经管缺陷之间的关联。在荷兰研究组中,但不在德克萨斯州研究组中,我们发现 MTHFR 的 DNA 甲基化水平与 NTD 风险之间存在显著关联(病例组中甲基化绝对值降低了-0.33%,P 值=0.001),LEKR/CCNL (甲基化绝对值增加:1.36%在病例中,P 值=0.048),以及 VANGL 存在边缘显著关联(病例中甲基化绝对值增加:0.17%,P 值=0.063)。仅在经过多次测试校正后,MTHFR 与 NTD 风险之间的关联仍然显著。在德克萨斯州的研究中没有复制荷兰研究的结果。我们得出的结论是,MTHFR 基因的甲基化与 NTD 之间的关联,以及 VANGL 和 LEKKR/CNNL 之间的关联,与先前的研究一致,这些研究显示同一基因的多态性与 NTD 和胚胎发育分别相关。