MTHFR、MTRR基因多态性与不良妊娠结局的相关性
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The relationships between MTHFR, MTRR gene polymorphisms and adverse pregnancy outcome
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    摘要:

    【摘要】目的 探讨亚甲基四氢叶酸还原酶(MTHFR)和甲硫氨酸合成还原酶(MTRR)基因多态性与不良妊娠结局的相关性。方法 选取2016年6月~2018年6月于西北妇女儿童医院接受治疗的有不良妊娠史孕妇88例作为研究对象(不良妊娠组),另选取同期在本院做产前检查结果正常的无不良妊娠结局史的孕妇95例作为对照组。不良妊娠结局包括胎儿宫内生长受限(IUGR)、胎死宫内、胎儿畸形、早产儿。通过Taqman MGB技术检测受试者血浆MTHFR基因C677T位点、MTRR基因A66G位点多态性分布频率;分析MTHFR基因C677T位点、MTRR基因A66G位点多态性与不良妊娠结局的关系。Logistic回归分析不良妊娠结局的影响因素。结果 MTHFR基因C677T位点存在野生CC型、杂合子CT型、纯合子TT型;MTRR基因A66G位点存在野生AA型、杂合子AG型、纯合子GG型。与对照组相比,不良妊娠组MTHFR基因C677T位点CT、TT基因型及T等位基因频率显著升高(P<0.05);MTRR基因A66G位点AG、GG及G等位基因频率显著升高(P<0.05)。MTHFR基因C677T位点野生CC型、杂合子CT型、纯合子TT型及MTRR基因A66G位点野生AA型、杂合子AG型、纯合子GG型患者IUGR、胎死宫内、胎儿畸形、早产儿发生率均依次升高,三组间比较差异有统计学意义(P<0.05)。MTHFR基因C677T位点杂合子CT型、纯合子突变TT型及MTRR基因A66G位点杂合子AG型、纯合子GG型是不良妊娠结局发生的危险因素(P<0.05)。结论 血浆中MTHFR及MTRR基因多态性与不良妊娠结局的发生密切相关,可以作为预测孕妇不良妊娠结局的指标。

    Abstract:

    【Abstract】Objective To investigate the relationship between methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and adverse pregnancy outcome. Methods From June 2016 to June 2018, 88 pregnant women with a history of adverse pregnancy in our hospital were selected as the study objects (adverse pregnancy group), and adverse pregnancy outcomes included intrauterine growth restriction (IUGR), intrauterine fetal death, fetal malformation and premature infants. In addition, 95 pregnant women with normal prenatal examination results and no adverse pregnancy outcome were selected as the control group. Taqman MGB technique was used to detect the distribution frequencies of C677T locus of MTHFR gene and A66G locus of MTRR gene in plasma; and the relationships between polymorphisms of C677T locus of MTHFR gene and A66G locus of MTRR gene and adverse pregnancy outcome were analyzed. In addition, the influencing factors of adverse pregnancy outcome were analyzed by Logistic regression. Results There were wild CC type, heterozygous CT type and homozygous TT type in C677T locus of MTHFR gene and there were wild AA type, heterozygous AG type and homozygous GG type in A66G locus of MTRR gene. Compared with those in the control group, the frequencies of CT, TT genotypes and T allele at C677T locus of MTHFR gene in the adverse pregnancy group were significantly higher (P<0.05). The frequencies of AG, GG and G allele at A66G locus of MTRR gene were significantly higher (P<0.05). The incidences of IUGR, intrauterine fetal death, fetal malformation and preterm infants in patients with wild CC type, heterozygous CT type and homozygous TT type at C677T locus of MTHFR gene, wild AA type, heterozygous AG type and homozygous GG type at A66G locus of MTRR gene in the three groups increased in turn, and the difference among the three groups was statistically significant (P<0.05). Heterozygous CT type and homozygous TT type at C677T locus of MTHFR gene, heterozygous AG type and homozygous GG type at A66G locus of MTRR gene were the risk factors of adverse pregnancy outcome (P<0.05). onclusion MTHFR and MTRR gene polymorphisms in plasma are closely related to the occurrence of adverse pregnancy outcomes, which may be used as an indicator to predict adverse pregnancy outcomes.

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  • 在线发布日期: 2021-06-03
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