血红素加氧酶1基因启动子区多态性与冠心病的相关性及其对血清胆红素水平的影响
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国家自然科学基金(30760263);新疆自治区重大专项课题(200733146-3)


Association Between Coronary Heart Disease and Heme Oxygenase-1 Promoter Region Polymorphism and the Influence of the Level of Serum Bilirubin
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    摘要:

    目的探讨冠心病患者血红素加氧酶1启动子区(GT)n重复序列多态性与冠心病的相关性及其对血清胆红素水平的影响。方法采用聚合酶链反应-非变性聚丙烯酰胺凝胶电泳法检测337例冠心病患者和240例健康对照者血红素加氧酶1启动子区(GT)n重复序列多态性,同时测定血清胆红素水平。结果冠心病组与对照组LL基因型及L等位基因频率分布差异显著(P<0.05);L等位基因频率在冠心病不同病变程度之间分布差异显著(P<0.05),且LL基因型频率在多支血管病变组较单支和双支血管病变组高(P<0.05);LL基因型者胆红素水平较SS基因型者明显下降(P<0.001)。结论血红素加氧酶1启动子区(GT)n重复序列多态性与冠心病的发生发展及冠状动脉狭窄程度有关,L等位基因是冠心病的一个危险因素,可能与该基因多态性所致血清胆红素水平降低有关。

    Abstract:

    Aim To investigate the association between coronary heart disease (CHD) and heme oxygenase-1 (HO-1) promoter region (GT)n repeated sequence polymorphism and the influence of the level of serum bilirubin. Methods The polymorphism of HO-1 gene in 337 CHD patients and 240 health controls was analyzed by polymerase chain reaction-native polyacrylamide gel electrophoresis,and the level of serum bilirubin of each patient at the same time was detected. Results The HO-1 genotypes were classified into three groups:LL,LS and SS. The LL genotypic frequency and L allele frequency in CHD patients was significantly higher than control group (P<0.05); the L allele frequency had different distribution in single,double and multivessel disease (P<0.05),and the LL genotypic frequency of multivessel disease patients was higher than that of single and double vessel disease patients (P<0.05); bilirubin level of LL genotype patients was significantly lower than that of SS genotype patients (P<0.001). Conclusions The polymorphism of HO-1 promoter region (GT)n repeated sequence plays an important role in CHD pathobiology process,L allele frequency is a risk factor of CHD,which maybe correlate with its potential ability to decrease the serum bilirubin.

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王迎洪,马依彤,付真彦,杨毅宁,谢翔,刘芬.血红素加氧酶1基因启动子区多态性与冠心病的相关性及其对血清胆红素水平的影响[J].中国动脉硬化杂志,2008,16(10):834~837.

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  • 收稿日期:2008-09-12
  • 最后修改日期:2008-10-01
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