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Association of genetic polymorphisms of folate cycle enzymes with risk of pregnancy complications 叶酸循环酶基因多态性与妊娠并发症风险的关系
Q2 Medicine Pub Date : 2023-01-01 DOI: 10.20953/1726-1678-2023-2-28-32
A.V. Putintseva, E.V. Shikh
Polymorphisms in the genes of folate cycle enzymes are considered as the main cause of reduced plasma levels of folate and vitamin B12, impaired homocysteine metabolism, and the development of pregnancy complications. Objective. To study the association of polymorphism in folate cycle enzyme genes, MTHFR-677C>T, MTHFR-1298A>C, MTR‑2756A>G, MTRR-66A>G, with the risk of pregnancy complications. Patients and methods. The study was conducted in outpatient settings and included 96 women aged between 20 and 40 years with a history of 1 to 3 pregnancies who applied for preconception care. Results. When examining the association between the presence of a complicated history in this group of women and folate cycle enzyme gene polymorphisms using the Fisher test, a statistically significant correlation was detected for MTHFR-677C>T, MTHFR-1298A>C, MTR-2756A>G, and MTRR-66A>G. Conclusion. The presence/absence of genetic polymorphisms of folate cycle enzymes should be considered when predicting the risks of pregnancy complications and developing a personalized preconception care program to select individual regimens of folate supplementation. Key words: genes, folate cycle, polymorphism, folates, pregnancy
叶酸循环酶基因的多态性被认为是血浆中叶酸和维生素B12水平降低、同型半胱氨酸代谢受损和妊娠并发症发生的主要原因。目标。研究叶酸循环酶基因MTHFR-677C>T、MTHFR-1298A>C、mthfr - 2756A>G、MTRR-66A>G多态性与妊娠并发症发生风险的关系。患者和方法。该研究在门诊进行,包括96名年龄在20至40岁之间,有1至3次怀孕史的妇女,她们申请了孕前护理。结果。当使用Fisher检验检查这组女性中存在的复杂病史与叶酸循环酶基因多态性之间的关系时,检测到MTHFR-677C>T、MTHFR-1298A>C、mthfr - 2756a>G和MTRR-66A>G具有统计学意义的相关性。结论。在预测妊娠并发症风险和制定个性化孕前护理计划以选择叶酸补充方案时,应考虑叶酸循环酶遗传多态性的存在/缺失。关键词:基因,叶酸周期,多态性,叶酸,妊娠
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Voprosy Ginekologii, Akusherstva i Perinatologii
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