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来庆国, 袁奎封, 罗圣磊, 杨中军, 徐欣. TGF-α基因多态性及叶酸与非综合征性唇腭裂关系[J]. 中国公共卫生, 2009, 25(6): 756-757. DOI: 10.11847/zgggws2009-25-06-59
引用本文: 来庆国, 袁奎封, 罗圣磊, 杨中军, 徐欣. TGF-α基因多态性及叶酸与非综合征性唇腭裂关系[J]. 中国公共卫生, 2009, 25(6): 756-757. DOI: 10.11847/zgggws2009-25-06-59
LAI Qing-guo, YUAN Kui-feng, LUO Sheng-lei, . Association of TGF-α gene polymorphism and folic acid supplementation with nonsyndromic cleft lip with or without cleft palate[J]. Chinese Journal of Public Health, 2009, 25(6): 756-757. DOI: 10.11847/zgggws2009-25-06-59
Citation: LAI Qing-guo, YUAN Kui-feng, LUO Sheng-lei, . Association of TGF-α gene polymorphism and folic acid supplementation with nonsyndromic cleft lip with or without cleft palate[J]. Chinese Journal of Public Health, 2009, 25(6): 756-757. DOI: 10.11847/zgggws2009-25-06-59

TGF-α基因多态性及叶酸与非综合征性唇腭裂关系

Association of TGF-α gene polymorphism and folic acid supplementation with nonsyndromic cleft lip with or without cleft palate

  • 摘要: 目的 研究山东汉族人转化生长因子-α(TGF-α)基因多态性及叶酸补充与非综合征性唇腭裂的关系。方法 通过问卷调查获得所有研究对象母亲孕前孕期叶酸补充等资料。应用多聚酶链反应(PCR)结合限制性酶切方法,确定199例非综合征性唇腭裂患者与203名正常人的基因型。将基因型与叶酸补充因素进行分析。结果 非综合征性唇腭裂患者TGF-α的C2等位基因频率明显高于正常对照组,差异有统计学意义(P<0.05);孕前孕期不补充叶酸的孕妇发生非综合征性唇腭裂增多,差异有统计学意义(P<0.05)。C1C2基因型与叶酸缺乏因素有交互作用。结论 TGF-α基因的突变及孕期叶酸缺乏与汉族人非综合征性唇腭裂的发生有相关性。含有C2等位基因的个体对孕期叶酸缺乏的危险因素更为敏感。

     

    Abstract: Objective To study the association of transfouning growth factor alpha (TGF-α)gene polymoiphisn and folic acid supplementation in Han nationality with nonsyndrom is cleft lip with or without cleft palate (NSCL/P).Methods Data related to folic acid supplementation during the periconceptional period were gained through investigation of patients' mothers Polymerase chain reaction combined with restrictenzyma digestion was used to detect the target gene variation in 199 patients with NSCL/P and 203 healthy controls.Analysis was carried on the genotype and folic acid supplementation.Results The C2 allele frequency in patients with NSCL/P was significantly higher than that of in healthy controll There was a significant increase of NSCL/P in infants with the mothers without folic acid supplem entation during the pregnatncy.There was an interaction between C1C2 genetype and folic acid supplem entation.Conclusion TGF-α gene polymoiphism is closely associated with NSCL/R Folic acid supplem entation during the periconceptional period is associated with the occurrence of NSCL/P.Individuals containing C2 allele are more sensitive to folic acid deficiency.

     

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