期刊文献+

母亲MTHFR 677C/T多态性和孕期状况与子代发生先天性心脏病的相关性研究 被引量:9

Correlation between offspring congenital heart disease and MTHFR 677C/T polymorphism and general status of pregnant women
原文传递
导出
摘要 目的 探讨母亲孕期MTHFR 677C/T多态性、孕期状况在子代先天性心脏病(CHD)发生中的相互关系.方法 采用病例对照研究,调查100对CHD胎儿和无CHD胎儿生物学母亲有关入口学、孕期环境相关情况、优生认知,并检测MTHFR 677C/T基因多态性以及血清同型半胱氨酸(HCY)、叶酸、VitB12水平,进行单因素和多因素非条件logistic回归分析.结果 病例组和对照组MTHFR 677C/T基因型和等位基因频率差异无统计学意义(χ^2=1.08,P=0.582;χ^2=0.53,P=0.468),血清HCY水平两组差异有统计学意义(t=-8.14,P=0.000).单因素分析,14个因素有统计学意义(P<0.05);多因素logistic逐步回归分析,母亲教育程度(OR=3.386,95%CI:1.279~8.961)、家庭年收入(OR=8.699,95%CI:2.177 ~ 34.765)、患慢性病(OR=0.343,95%CI:0.134~0.881)、优生认知得分(OR=0.906,95%CI:0.836 ~ 0.981)、血清HCY水平(OR=1.734,95%CI:1.458 ~ 1.986)、异常生育史(OR=3.710,95%CI:1.217 ~ 11.308)等因素与子代CHD相关.结论 母亲MTHFR 677C/T多态性与子代CHD发生未发现关联;母亲教育程度低、家庭年收入低、异常生育史、优生认知得分低、血清HCY水平高可能增加子代CHD的发生危险. Objective To understand the relationship between MTHFR 677C/T polymorphism and general status of pregnant women and offspring congenital heart disease (CHD).Methods A case-control study was conducted among the biological mothers of 100 infants with CHD and 100 healthy controls to collect the information about their demographic characteristics,general status during pregnancy and awareness of eugenics.Their MTHFR 677C/T polymorphism and serum homocysteine (HCY),folic acid,vitamin B12 levels were detected.Results The differences in MTHFR genotype and allele frequency between the two groups were not statistical significant (χ^2=1.08,P=0.582;χ^2=0.53,P=0.468),but the difference in serum HCY between two groups were statistical significant (t=-8.14,P=0.000).Univariate analysis showed that 14 factors had statistical significances (P〈0.05).Multivariate logistic regression analysis indicated that mother's educational level(OR=3.386,95% CI:1.279-8.961),annual household income (OR =8.699,95% CI:2.177-34.765),chronic disease prevalence (OR=0.343,95% CI:0.134-0.881),awareness of eugenics (OR=0.906,95% CI:0.836-0.981),serum HCY level(OR=1.734,95%CI:1.458-1.986) and abnormal reproductive history(OR=3.710,95% CI:1.217-11.308) were correlated with offspring CHD.Conclusion There was no correlation between MTHFR 677C/T polymorphism of pregnant women and offspring CHD,but low educational level,low annual household income,abnormal reproductive history,low awareness of eugenics and high serum HCY levels of pregnant women might increase the risk of offspring CHD.
出处 《中华流行病学杂志》 CAS CSCD 北大核心 2015年第10期1072-1076,共5页 Chinese Journal of Epidemiology
基金 浙江省公益技术研究社会发展项目(2012C23092) 浙江省医药卫生一般研究项目(2012KYA049)
关键词 先天性心脏病 亚甲基四氢叶酸还原酶 基因 孕期状况 Congenital heart disease Methylenetetrahydrofolate reductase Gene General status during pregnancy
  • 相关文献

参考文献12

二级参考文献137

共引文献210

同被引文献49

  • 1王苏梅,王磊光.亚甲基四氢叶酸还原酶基因多态性与出生缺陷[J].国外医学(计划生育分册),2005,24(1):39-41. 被引量:6
  • 2李勇,成君,朱文丽,刀京晶,闫丽盈,李孟忆,李书琴.先天性心脏病核心家庭血清同型半胱氨酸水平及相关基因多态性研究[J].北京大学学报(医学版),2005,37(1):75-80. 被引量:12
  • 3朱文丽,刀京晶,成君,李书琴,李勇.血清同型半胱氨酸及叶酸水平与先天性心脏病的关系[J].卫生研究,2005,34(6):740-743. 被引量:12
  • 4钟秋安,仇小强,曾小云,林娜娜.父母MTHFR基因、CBS基因与子代先天性心脏病关系的研究[J].广西医学,2006,28(8):1140-1142. 被引量:8
  • 5中华人民共和国卫生部.《中国出生缺陷防治报告(2012)》[R].2012,9:1.
  • 6Wallingford JB, Niswander LA, Shaw GM, et al. The continuing challenge of understanding, preventing, and treating neural tube defects [ J ]. Science, 2013,339 ( 6123 ) : 1222002.
  • 7Yu D, Yang L, Shen S,et al. Association between methionine syn- thase reductase A66G polymorphism and the risk of congenital heart defects : evidence from eight case-control studies [ J ]. Pediatr Cardiol,2014,35 (7) : 1091-1098.
  • 8Cai B, Zhang T, Zhong R,et al. Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease : an in- tegrated meta-analysis [ J ]. PLoS One, 2014,9 ( 3 ) : e89609.
  • 9Copped~ F. The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects[J]. Front Genet,2015, 6:223.
  • 10Mamasoula C, Prentice RR, Pierscionek T, et al. Association be- tween C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13, 125 controls[ J]. Circ Cardiovasc Genet, 2013,6 (4) : 347-53.

引证文献9

二级引证文献47

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