Balduino Victorino Daniella, de Godoy Moacir Fernandes, Goloni-Bertollo Eny Maria, Pavarino Érika Cristina
Unidade de Pesquisa em Genética e Biologia Molecular (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP), Avenida Brigadeiro Faria Lima No. 5416, Bloco U-6, 15090-000 São José do Rio Preto, SP, Brazil.
Núcleo Transdisciplinar para Estudo do Caos e da Complexidade (NUTECC), Faculdade de Medicina de São José do Rio Preto (FAMERP), 15090-000 São José do Rio Preto, SP, Brazil.
Dis Markers. 2014;2014:517504. doi: 10.1155/2014/517504. Epub 2014 Dec 4.
Inconclusive results of the association between genetic polymorphisms involved in folate metabolism and maternal risk for Down syndrome (DS) have been reported. Therefore, this meta-analysis was conducted. We searched electronic databases through May, 2014, for eligible studies. Pooled odds ratios with 95% confidence intervals were used to assess the strength of the association, which was estimated by fixed or random effects models. Heterogeneity among studies was evaluated using Q-test and I (2) statistic. Subgroup and sensitivity analyses were also conducted. Publication bias was estimated using Begg's and Egger's tests. A total of 17 case-controls studies were included. There was evidence for an association between the MTRR c.66A>G (rs1801394) polymorphism and maternal risk for DS. In the subgroup analysis, increased maternal risk for DS was found in Caucasians. Additionally, the polymorphic heterozygote MTHFD1 1958GA genotype was associated significantly with maternal risk for DS, when we limit the analysis by studies conformed to Hardy-Weinberg equilibrium. Finally, considering MTR c.2756A>G (rs1805087), TC2 c.776C>G (rs1801198), and CBS c.844ins68, no significant associations have been found, neither in the overall analyses nor in the stratified analyses by ethnicity. In conclusion, our meta-analysis suggested that the MTRR c.66A>G (rs1801394) polymorphism and MTHFD1 c.1958G>A (rs2236225) were associated with increased maternal risk for DS.
已有报道称,参与叶酸代谢的基因多态性与唐氏综合征(DS)产妇风险之间的关联结果尚无定论。因此,我们进行了这项荟萃分析。我们检索了截至2014年5月的电子数据库,以查找符合条件的研究。采用合并比值比及95%置信区间来评估关联强度,该强度通过固定效应模型或随机效应模型进行估计。使用Q检验和I²统计量评估研究间的异质性。还进行了亚组分析和敏感性分析。采用Begg检验和Egger检验估计发表偏倚。共纳入17项病例对照研究。有证据表明甲硫氨酸合成酶还原酶(MTRR)基因c.66A>G(rs1801394)多态性与DS产妇风险之间存在关联。在亚组分析中,发现高加索人群中DS产妇风险增加。此外,当我们将分析限制在符合哈迪-温伯格平衡的研究中时,亚甲基四氢叶酸脱氢酶1(MTHFD1)基因1958GA基因型多态性杂合子与DS产妇风险显著相关。最后,对于甲硫氨酸合成酶(MTR)基因c.2756A>G(rs1805087)、亚甲基四氢叶酸还原酶2(TC2)基因c.776C>G(rs1801198)和胱硫醚β合成酶(CBS)基因c.844ins68,在总体分析和按种族分层分析中均未发现显著关联。总之,我们的荟萃分析表明,MTRR基因c.66A>G(rs1801394)多态性和MTHFD1基因c.1958G>A(rs2236225)与DS产妇风险增加有关。