首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Reduced folate carrier A80G polymorphism and susceptibility to neural tube defects: A meta-analysis
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Reduced folate carrier A80G polymorphism and susceptibility to neural tube defects: A meta-analysis

机译:叶酸载体A80G多态性降低和对神经管缺陷的易感性:荟萃分析

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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.
机译:减少的叶酸载体(RFC1)在介导叶酸传递到各种细胞中起着至关重要的作用。据报道,RFC1多态性(A80G)与神经管缺损(NTD)的风险增加有关。但是,从个人能力不足的研究中得出的结果相互矛盾。我们对MEDLINE和EMBASE数据库进行了系统搜索,并对RFC1多态性(A80G)与NTD风险之间的关联进行了荟萃分析。总体而言,在婴儿和母亲中均未发现RFC1 A80G多态性与NTD风险之间存在显着相关性(婴儿等位基因对比:OR RE = 1.15,95%CI:0.92-1.45;母亲等位基因对比:OR RE = 1.24,95 %CI:0.98-1.56)。当前的荟萃分析未能支持RFC1 A80G多态性与NTD易感性之间的正相关。然而,重要的是要意识到,社会经济因素以及基因环境和基因-基因相互作用可能会影响我们的荟萃分析的结果。因此,A80G多态性与NTD风险之间的关系无法完全消除。

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