Department of Pharmacy, Qilu Hospital, Shandong University, Jinan, China.
Gene. 2012 Dec 1;510(2):180-4. doi: 10.1016/j.gene.2012.02.020. Epub 2012 Sep 10.
The reduced folate carrier (RFC1) plays a crucial role in mediating folate delivery into a variety of cells. RFC1 polymorphism (A80G) has been reported to be associated with increased risk of neural tube defects (NTDs). However, results derived from individually underpowered studies are conflicting. We performed a systematic search of MEDLINE and EMBASE databases and carried out a meta-analysis on the association between RFC1 polymorphism (A80G) and NTDs risk. Overall, a significant correlation between RFC1 A80G polymorphism and NTDs risk was found neither in infants nor in maternal (allele contrast in infants: OR(RE)=1.15, 95% CI: 0.92-1.45; allele contrast in mothers: OR(RE)=1.24, 95% CI: 0.98-1.56). The present meta-analysis failed to support a positive association between RFC1 A80G polymorphism and susceptibility to NTDs. It is important to realize, however, that socio-economic factors, and gene-environment and gene-gene interactions, could have influenced the outcome of our meta-analysis. For this reason, a relationship between the A80G polymorphism and NTD risk cannot be entirely discounted.
还原叶酸载体(RFC1)在介导叶酸进入各种细胞中起着至关重要的作用。RFC1 多态性(A80G)已被报道与神经管缺陷(NTDs)风险增加有关。然而,来自单独的研究的结果存在冲突。我们对 MEDLINE 和 EMBASE 数据库进行了系统搜索,并对 RFC1 多态性(A80G)与 NTDs 风险之间的关联进行了荟萃分析。总体而言,无论是在婴儿还是在母亲中,RFC1 A80G 多态性与 NTDs 风险之间均无显著相关性(婴儿的等位基因对比:OR(RE)=1.15,95%CI:0.92-1.45;母亲的等位基因对比:OR(RE)=1.24,95%CI:0.98-1.56)。本荟萃分析未能支持 RFC1 A80G 多态性与 NTDs 易感性之间存在正相关。然而,需要认识到,社会经济因素、基因-环境和基因-基因相互作用可能影响了我们荟萃分析的结果。因此,A80G 多态性与 NTD 风险之间的关系不能完全排除。