[1]杜濛濛,金春燕,顾志萍.孕妇叶酸代谢关键基因位点多态性与早产的关系[J].新乡医学院学报,2022,39(12):1168-1172.[doi:10.7683/xxyxyxb.2022.12.013]
 DU Mengmeng,JIN Chunyan,GU Zhiping.Relationship between polymorphism of key gene locus of folic acid metabolism and premature delivery in pregnant women[J].Journal of Xinxiang Medical University,2022,39(12):1168-1172.[doi:10.7683/xxyxyxb.2022.12.013]
点击复制

孕妇叶酸代谢关键基因位点多态性与早产的关系
分享到:

《新乡医学院学报》[ISSN:1004-7239/CN:41-1186/R]

卷:
39
期数:
2022年12
页码:
1168-1172
栏目:
临床研究
出版日期:
2022-12-05

文章信息/Info

Title:
Relationship between polymorphism of key gene locus of folic acid metabolism and premature delivery in pregnant women
作者:
杜濛濛金春燕顾志萍
(南京医科大学附属泰州人民医院医学遗传与产前诊断科,江苏 泰州 225300)
Author(s):
DU MengmengJIN ChunyanGU Zhiping
(Department of Medical Genetics and Prenatal Diagnosis,Taizhou People′s Hospital Affiliated to Nanjing Medical University,Taizhou 225300,Jiangsu Province,China)
关键词:
早产基因多态性叶酸代谢关键基因
Keywords:
preterm birthgene polymorphismkey gene of folic acid metabolism
分类号:
R714;R394
DOI:
10.7683/xxyxyxb.2022.12.013
文献标志码:
A
摘要:
目的 分析孕妇叶酸代谢关键基因位点多态性的分布情况及其与早产的关系。方法 回顾性分析221例于2020年1月至2021年1月在南京医科大学附属泰州人民医院建立孕检档案并在孕早期做叶酸代谢关键基因筛查者的临床资料。根据孕妇分娩结果将研究对象分为早产组(n=125)和正常分娩组(n=96)。采用金磁微粒层析法检测2组受试者的叶酸代谢关键基因5,10-亚甲基四氢叶酸还原酶(MTHFR)C677T位点基因多态性。比较2组受试者一般资料及基因型分布情况。采用多因素logistic回归分析影响孕妇发生早产的危险因素。结果 早产组孕妇的年龄、体质量指数、文化程度、孕前3个月配偶是否吸烟、孕前3个月配偶是否酗酒、家庭经济情况、工作、孕次、自然流产史及人工流产史等情况与正常分娩组比较差异无统计学意义(P>0.05)。早产组中居住在乡村、有妊娠高血压综合征、通过人工辅助生殖技术怀孕、孕前补充叶酸时间为1个月及有孕期服药史者所占比例显著高于正常分娩组(P<0.05);早产组受试者的叶酸水平显著低于正常分娩组(P<0.05)。早产组与正常分娩组受试者MTHFR基因C677T位点基因型和等位基因的分布频率比较差异有统计学意义(P<0.05)。多因素logistic回归分析结果显示,MTHFR基因C677T位点CC基因型及等位基因T的分布频率是孕妇发生早产的危险因素(P<0.05)。结论 孕妇叶酸代谢关键基因MTHFR C677T位点基因型及等位基因分布频率是孕妇发生早产的危险因素。
Abstract:
Objective To analyze the distribution of polymorphism of key gene locus of folic acid metabolism in pregnant women and its relationship with premature delivery.Methods The clinical data of 221 pregnant who were established with pregnancy examination files in Taizhou People′s Hospital Affiliated to Nanjing Medical University from January 2020 to January 2021 and screened for key genes of folic acid metabolism in early pregnancy were analyzed retrospectively.The pregnant women were divided into premature delivery group (n=125) and normal delivery group (n=96) according to the delivery results.The general data and genotype distribution of subjects in the two groups were compared.The gene polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T locus in the key gene of folic acid metabolism of subjects in the two groups was detected.The risk factors of premature delivery in pregnant women were analyzed by multivariate logistic regression.Results There was no significant difference in the age,body mass index,education level,whether the spouse smoked in the first three months of pregnancy,whether the spouse drank excessively in the first three months of pregnancy,family economic situation,whether the pregnant woman work,pregnancy times,history of spontaneous abortion and history of induced abortion between the preterm delivery group and the normal delivery group (P>0.05).The proportions of living in the countryside,having pregnancy-induced hypertension syndrome,being pregnant through artificial assisted reproductive technology,taking folic acid for one month before pregnancy and taking medicine during pregnancy in the premature delivery group were significantly higher than those in the normal delivery group (P<0.05);the level of folic acid of subjects in the premature delivery group was significantly lower than that in the normal delivery group (P<0.05).There was significant difference in the distribution frequency of genotype and allele of MTHFR gene C677T locus between the preterm delivery group and the normal delivery group (P<0.05).Multivariate logistic regression analysis showed that the distribution frequency of CC genotype and allele T at C677T locus of MTHFR gene were risk factors for premature delivery in pregnant women (P<0.05).Conclusion The distribution of genotype and allele of MTHFR gene C677T locus of key genes of folic acid metabolism in pregnant women are the risk factor for premature delivery in pregnant women.

参考文献/References:

[1] VOGEL J P,CHAWANPAIBOON S,MOLLER A B,et al.The global epidemiology of preterm birth[J].Best Pract Res Clin Obstet Gynaecol,2018,52(10):3-12.
[2] HEDDERICH D M,BOECKH-BEHRENS T,BUML J G,et al.Sequelae of premature birth in young adults:incidental findings on routine brain MRI[J].Clin Neuroradiol,2021,31(2):325-333.
[3] OPHELDERS D R M G,GUSSENHOVEN R,KLEIN L,et al.Preterm brain injury,antenatal triggers,and therapeutics:timing is key[J].Cells,2020,9(8):1871.
[4] KWON B N,LEE N R,KIM H J,et al.Folate metabolizing gene polymorphisms and genetic vulnerability to preterm birth in Korean women[J].Genes Genomics,2021,43(8):937-945.
[5] MAO Y Y,YANG L,LI M,et al.Periconceptional folic acid supplementation and the risk of spontaneous abortion among women who prepared to conceive:impact of supplementation initiation timing[J].Nutrients,2020,12(8):2264.
[6] 折开娥,秦利,张凌燕.MTHFR C677T基因多态性与胎儿神经管畸形关系[J].中国计划生育学杂志,2020,28(6):885-888.
SHE K E,QIN L,ZHANG L Y.Relationship between MTHFR C677T gene polymorphism and fetal neural tube malformation[J].Chin J Fam Plan,2020,28(6):885-888.
[7] KHALIFE S,BISSAR-TADMOURI N.Inherited thrombophilia in a lebanese family of four generations:acase report of recurrent miscarriage[J].Vasc Health Risk Manag,2020,21(16):53-56.
[8] ZHANG Y,HE X,XIONG X,et al.The association between maternal methylenetetrahydrofolate reductase C677T and A1298C polymorphism and birth defects and adverse pregnancy outcomes[J].Prenat Diagn,2019,39(1):3-9.
[9] WADON M,MODI N,WONG H S,et al.Recent advances in the genetics of preterm birth[J].Ann Hum Genet,2020,84(3):205-213.
[10] QIN J,LI J,LI F,et al.Association of maternal folate use and reduced folate carrier gene polymorphisms with the risk of congenital heart disease in offspring[J].Eur J Pediatr,2021,180(10):3181-3190.
[11] SATA F,YAMADA H,KISHI R,et al.Maternal folate,alcohol and energy metabolism-related gene polymorphisms and the risk of recurrent pregnancy loss[J].J Dev Orig Health Dis,2012,3(5):327-332.
[12] WANG W,JIAO X H,WANG X P,et al.MTR,MTRR,and MTHFR gene polymorphisms and susceptibility to nonsyndromic cleft lip with or without cleft palate[J].Genet Test Mol Biomarkers,2016,20(6):297-303.
[13] VANDER WINDT M,SCHOENMAKERS S,VAN RIJN B,et al.Epidemiology and (patho)physiology of folic acid supplement use in obese women before and during pregnancy[J].Nutrients,2021,13(2):331.
[14] 劳海红,贺宪民.海南省汉族和黎族妇女亚甲基四氢叶酸还原酶和甲硫氨酸合成酶还原酶基因多态性分布研究[J].中国计划生育学杂志,2011,19(11):655-657.
LAO H H,HE X M.Study on methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphism among the Han and Li women in Hainan province [J].Chin J Fam Plan,2011,19(11):655-657.
[15] 从玉英,鲁衍强,芮欣忆,等.淄博市汉族女性亚甲基四氢叶酸还原酶和甲硫氨酸合成酶还原酶基因多态性分布研究[J].现代妇产科进展,2012,21(10):779-781.
CONG Y Y,LU Y Q,RUI X Y,et al.Polymorphisms of methylenetetrahydrofolate reductase and methionine synthase reductase genes in Han women in Zibo City[J].Prog Obstet Gynecol,2012,21(10):779-781.
[16] 王连,郝胜菊,毛宝宏,等.兰州地区育龄妇女叶酸代谢与早产的相关性研究[J].中国妇幼保健,2019,34(6):1234-1236.
WANG L,HAO S J,MAO B H,et al.Study on the correlation between folic acid metabolism and premature delivery in women of childbearing age in Lanzhou region[J].Matern Child Health Care China,2019,34(6):1234-1236.
[17] ZHANG L,FU H,WEI T.MTHFR gene polymorphism and homocysteine levels in spontaneous abortion of pregnant women[J].Am J Transl Res,2021,13(6):7083-7088.
[18] TURGAL M,GUMRUK F,KARAAGAOGLU E,et al.Methylenetetrahydrofolate reductase polymorphisms and pregnancy outcome[J].Geburtshilfe Frauenheilkd,2018,78(9):871-878.

相似文献/References:

[1]廖 娜,张合喜.幽门螺杆菌及宿主基因特征与胃肠疾病关系[J].新乡医学院学报,2006,23(05):533.
[2]郭娟宁,千新来,樊爱英,等.肿瘤坏死因子受体基因多态性与扩张型心肌病遗传易感性的关系[J].新乡医学院学报,2009,26(02):150.
 GUO Juan-ning,QIAN Xin-lai,FAN Ai-ying,et al.Association of the tumor necrosis factor receptor gene polymorphisms with the genetic susceptibility to dilated cardiomyopathy[J].Journal of Xinxiang Medical University,2009,26(12):150.
[3]李艳,黄新恩,陈颖波,等.XPD751和XRCC1399联合基因型与非小细胞肺癌化疗毒性的关系[J].新乡医学院学报,2010,27(03):230.
[4]汪勇芬.早产儿的早期微量喂养[J].新乡医学院学报,2010,27(04):386.
[5]黄艳丽,覃小敏,邢 辉. 胰岛素样生长因子结合蛋白1检测联合宫颈超声检查在早产预测中的价值 [J].新乡医学院学报,2015,32(02):163.[doi:10.7683/xxyxyxb.2015.02.019]
[6]宫艳艳,王莉,陈苗,等.亚甲基四氢叶酸还原酶基因多态性与原因不明复发性流产的关系[J].新乡医学院学报,2022,39(12):1134.[doi:10.7683/xxyxyxb.2022.12.006]
 GONG Yanyan,WANG Li,CHEN Miao,et al.Relationship between methylene tetrahydrofolate reductase gene polymorphism and unexplained recurrent spontaneous abortion[J].Journal of Xinxiang Medical University,2022,39(12):1134.[doi:10.7683/xxyxyxb.2022.12.006]
[7]韩 俊,覃秋萍,郑颖惠. 宫颈环扎术治疗宫颈机能不全疗效分析[J].新乡医学院学报,2015,32(08):756.
[8]黄 蓉,邓宇傲,王 玲,等.CYP17基因多态性与子宫内膜异位症的相关性[J].新乡医学院学报,2017,34(2):129.[doi:10.7683/xxyxyxb.2017.02.013]
 HUANG Rong,DENG Yu-ao,WANG Ling,et al.Relationship between CYP17 gene polymorphism and endometriosis[J].Journal of Xinxiang Medical University,2017,34(12):129.[doi:10.7683/xxyxyxb.2017.02.013]
[9]齐光照,李朵璐.细胞色素P450酶CYP2W1研究进展[J].新乡医学院学报,2019,36(7):698.[doi:10.7683/xxyxyxb.2019.07.025]
[10]刘 峰,张颖莹,齐华林,等.过氧化物酶体增殖物激活受体γPro12Ala基因多态性与慢性肾脏病危险因素的关系[J].新乡医学院学报,2014,31(05):328.[doi:10.7683/xxyxyxb.2014.05.003]

更新日期/Last Update: 2022-12-05