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孕期个体化补充叶酸预防胎儿神经管缺陷效果观察 被引量:8

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摘要 目的观察孕期个体化补充叶酸预防胎儿神经管缺陷的效果。方法采用病例对照的方法,对900例孕妇实施传统补充叶酸(对照组),另1 992例孕妇实施个体化补充叶酸(观察组),比较两组孕妇血浆同型半胱氨酸(Hcy)及叶酸的浓度,随访其胎儿神经管缺陷的发病情况。结果观察组孕妇血浆Hcy水平降低、叶酸水平升高,中高风险度的胎儿神经管缺陷的发病率降低(P均<0.05)。结论个体化补充叶酸有助于预防神经管缺陷的发生。
出处 《山东医药》 CAS 2013年第30期72-73,共2页 Shandong Medical Journal
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参考文献14

  • 1肖坤则,张芝燕.中国神经管缺陷的流行病学[J].中华医学杂志,1989,69(4):189-191. 被引量:60
  • 2Chango A,Boisson F,Barbe F. The effect of 677C→T and 1298 A→C mutations plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects[J].British Journal of Nutrition,2000,(06):593-596.
  • 3Weisberg IS,Jacques PF,Selhub J. The 1298A→C polymorphism in methylenetetrahydrofolate reductase (MTHFR):in vitro expression and association with homocysteine[J].Atherosclerosis,2001,(02):409-415.doi:10.1016/S0021-9150(00)00671-7.
  • 4Han IB,Kim OJ,Ahn JY. Association of methylenetrahydrofolate reductase (MTHFR 677C 》 T and 1298A 》 C)polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population[J].Yonsei Medical Journal,2010,(02):253-260.
  • 5李智文,王丽娜.同型半胱氨酸代谢与神经管畸形[J].国外医学(卫生学分册),2002,29(5):269-273. 被引量:3
  • 6Nishio K,Goto Y,Kando T. Serum folate and methyleuetetrahydrofolate reductase (MTHFR)C677T polymorphisnl adjusted for folate intake[J].Journal of Epidemiology,2008,(03):125-131.
  • 7Brown CA,McKinney KQ,Kaufman JS. A common polymorphism in methionine synthase reductase increase risk of premature eoronary arterydisease[J].Journal of Cardiovascular Risk,2000,(03):197-200.
  • 8Gos M,Sliwerska E,Szpecht-Potocka A. Mutation incidence in folate metabolism genes and regulatory gene in Polish families with neural tube ddects[J].Journal of Applied Genetics,2004,(03):363-368.
  • 9Steergers-Theunissen RPM,Boers GHJ,Trijbels FJM. Maternal hyperhomcoysteinemia:a risk factor for neural-tube defects[J].Metabolism-Clinical and Experimental,1994,(12):1475-1480.
  • 10Mills JL,McPartlin JM,Kirke PN. Homcoysteine metabolism in pregnancies complicated by neural tube defects[J].The Lancet,1995,(8943):149-151.

二级参考文献31

共引文献146

同被引文献71

  • 1崔玲,周秀萍,崔豫琳,郭华峰.郑州市围产儿神经管畸形监测分析[J].中国公共卫生,2007,23(8):996-997. 被引量:7
  • 2于延辉,鲁衍强,李瑛,等.延边朝鲜族自治州汉族女性和朝鲜族女性MTHFR与MTRR基因多态性分布研究[J].实用医学杂志,2014,30(5):7-9.
  • 3Cooper DS. Doherty GM, Haugen BR, et al. Management guidelines for patients with thyroid nodules and differentiated thyroid cancer [J]. Thyroid, 2006,16(2) : 109-142.
  • 4Yeung MJ, Serpell JW. Management of the solitary thyroid nodule [J]. Oncologist, 2008,13(2) : 105-112.
  • 5Kim MJ, Kim EK, Kwak JY, et al. Differentiation of thyroid nodules with macrocalcifications: role of suspicious sonograph- icfindings[J]. Ultrasound Med, 2008,27(8):1179-1184.
  • 6Nishio K,Goto Y, Kando T, et al. Serum folate and methyl- euetetrahydrofolatereduetase ( MTHFR ) C677T polymor- phisnl adjusted for folate intake[J]. J Epidemiol, 2008, 18 (3) : 125-131.
  • 7Benrahma H, Abidi O, Melouk L, et al. Association of the C677T Polymorphism in the Human Methylenetetrahydrofo- late Reductase (MTHFR) Gene with the Genetic Predisposi- tion for Type 2 Diabetes Mellitus in a Moroccan Population [J]. Genet Test Mol Biomarkers, 2012 ,16(5):383-387.
  • 8Nishio K, Goto Y, Kondo T, et al. Serum folate and methyle- netetrahydrofolate reductase (MTHFR) C677T polymorphism adjusted tot folate intake [J]. J Epidemiol, 2008, 18 (3) : 125-131.
  • 9Cao Y, Xu J, Zhang Z, et al. Association study between meth- yleneterahydrofolate reductase polyomrphisms and unexplained recurrent pregnancy loss: a meta-analysis [J]. Gene, 2013, 514 (2): 105-111.
  • 10Ali A, Singh SK, Raman R. MTHFR 677TT alone and IRF6 820GG together with MTHFR 677CT, but not MTHFR A1298C, are risks for nonsyndromic cleft lip with or without cleft palate in an Indian population [J]. Genet Test Mol Bio- ma, 2009, 13 (3): 355-360.

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