期刊文献+

无锡女性MTHFR和MTRR基因多态性研究 被引量:6

Polymorphism analysis of MTHFR and MTRR among women in Wuxi
下载PDF
导出
摘要 目的分析无锡女性叶酸代谢相关基因MTHFR与MTRR的基因多态性分布特征。方法对无锡市524名育龄妇女,采集口腔黏膜上皮细胞,提取基因组DNA,用荧光定量PCR方法对MTHFR与MTRR基因多态性位点进行检测分析,了解无锡市妇女MTHFR与MTRR基因单核苷酸位点多态性(SNP)的分布频度,并与山东、河南、广东、海南等地区进行比较。结果无锡地区妇女MTHFR C677T位点多态性分布与山东、河南、广东、海南地区数据比较差异均有统计学意义(P均<0.05);MTHFR A1298C位点等位基因C出现频率低于等位基因A,与广东、海南地区数据比较差异均有统计学意义(P<0.01)。MTRR A66G位点多态性的分布与山东、河南、广东等地区数据比较差异无统计学意义(P均>0.05)。结论无锡地区女性MTHFR基因多态性分布具有地区特异性。 Objective To analyze genotype distributions of folic acid metabolic associated genes MTHFR and MTRR in Wuxi women. Method Five hundred and twenty-four women of childbearing age were recruited in this study. Genomic DNA was collected from their oral epithelial cells and detected by quantitative fluorescence PCR. The SNPs frequencies of MTHFR and MTRR were analyzed,and then were compared with that of Shandong,Henan,Guangdong and Hainan. Results The frequencies of MTHFR C677T in Wuxi women were significantly different from Shandong,Henan,Guangdong and Hainan (P〈0.05 ). The C allele frequency of MTHFR A1298C was lower than A allele among women in Wuxi,and it was different from Guang-dong and Hainan (P〈0.01). There was no significant difference of MTRR A66G polymorphism distribution between Wuxi and the other provinces (Such as Shandong,Henan and Guangdong etc),P〉0.05. Conclu-sions Distribution of MTHFR polymorphism in Wuxi women is region specific.
出处 《新医学》 2014年第4期253-257,共5页 Journal of New Medicine
关键词 无锡 亚甲基四氢叶酸还原酶 甲硫氨酸合成酶还原酶 基因多态性 Wuxi Methylenetetrahydrofolate reductase 5-methyltetrahydrofolate-homocysteine methyltransferase reductase Gene polymorphism
  • 相关文献

参考文献20

二级参考文献119

共引文献210

同被引文献133

  • 1谢佳莹,祁佳,宋铭,李育林,王迪,贾旭,张薇,钟明,尚嫄嫄.血清蛋白质β-折叠水平与冠心病的相关性[J].山东大学学报(医学版),2022,60(1):21-26. 被引量:2
  • 2李竹,严仁英,秦新华,彭瑞骢,钱宇平,渠川琰,李天霖,唐仪.论在我国推广“妇女增补叶酸预防神经管畸形”成果的必要性和适时性[J].中国优生优育(1990-2002上半年),1994,5(1):33-37. 被引量:27
  • 3毛仁芳,范义辉,白静,傅松滨.亚甲基四氢叶酸还原酶基因多态性及其与疾病的关系[J].国际遗传学杂志,2007,30(1):39-44. 被引量:10
  • 4王伟华,王凤菊,刘伟.MTRR基因A66G多态性与高同型半胱氨酸血症的相关性研究[J].山东医药,2007,47(25):54-55. 被引量:8
  • 5Ghassibe-Sabbagh M, Platt DE, Youhanna S, et al: Genetic and environmental influences on total plasma homocysteine and its rolein coronary artery diseaserisk[J]. Atherosclerosis ,2012,222(1) : 180-186.
  • 6Pavlovic AM, Pekmezovic T, Obrenovic R, et al: In creased total ho-mocysteine level is associated withclinical status and severity of white matter challges in symptomatic patients with subcortical small vessel dis- ease[J]. Clin Neurol Neurosurg, 2011, 13 (9) : 711- 715.
  • 7Beard RS, Reynolds J J, Bearden SE. Metabotropic glu- tamate receptor 5 mediates phosphorylation of vascular endothelial cadherin and nuclear localization of I3-cate- nin in response to homocysteine[J]. Vascul Pharma- col, 2012,56 (3-4) : 159-167.
  • 8Heil SG, Lievers KJ, Boers GH, et al: Betaine-homo- cysteine methyltransferase (BHMT) : genomic sequen- cing and relevance to hyperhomocysteinemia and vas- cular disease in humans[-J]. Mol Genet Metab ,2000,71 (3) :511-519.
  • 9Lajin B, Alachkar A, Sakur AA. Triplex tetra-primer ARMS-PCR method for the simultaneous detection of MTHFR c.677CT and c. 1298AC, and MTRR c. 66A G Polymorphisms of the folate-homocysteine metabolic pathway[J]. Mol Cell Probes, 2012,26 ( 1 ) : 16-20.
  • 10Guant-Rodriguez RM, JuilliSre Y, Candito M, et al:Association of MTRR A66G polymorphism (but not of MTHFR C677T and A1298C, MTR A2756G, TCN C776G) with homocysteine and coronary artery disease in the French population[J]. Thromb Haemost, 2005, 94(3) :510-515.

引证文献6

二级引证文献27

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部