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IL-18基因启动子-607C/A位点多态性与冠心病关系的研究

朱名安 吕军 宋惠 刘兴晖 朱静

湖北医药学院学报2011,Vol.30Issue(5):471-474,479,5.
湖北医药学院学报2011,Vol.30Issue(5):471-474,479,5.

IL-18基因启动子-607C/A位点多态性与冠心病关系的研究

Study on the Correlation Between Interleukin(IL)-18 gene Promoter-607 A/C Polymorphism and Risk of CHD

朱名安 1吕军 2宋惠 1刘兴晖 3朱静1

作者信息

  • 1. 湖北医药学院附属太和医院检验部,湖北十堰442000
  • 2. 湖北医药学院基础医学院,湖北十堰442000
  • 3. 附属东风医院检验科,湖北十堰442000
  • 折叠

摘要

Abstract

Objective To investigate the correlation between interleukin( IL)-18 gene promoter-607 A/C polymorphism and the risk of CHD in Chinese Han population. Methods The single nucleotide polymorphism at the position of interleukin (IL)-18 gene promoter -607 A/C were detected by sequence specific priroer-polymerase chain reaction (SSP-PCR) in 141 patients with CHD and 240 healthy controls. The genotype and allele frequencies were analyzed in both CHD group and control group. Meanwhile,the blood lipids were measured by enzyme method. Results In CHD group and control group,the CC, CA.AA genotype frequencies of IL-18 gene promoter-607C/A were 33.3% ,50.4% ,16.3% and 21.3% ,51.3% ,27.4%, respectively;the C,A allele frequencies were 58.5% ,41.5% and 46.9% ,53.1% ,respectively. The frequency of genotype CC and allele C at position -607 C/A of CHD group were significantly higher than those of control group( x2 = 4.56, P = 0. 03 and x2 =7.49, P=0.01 .respectively). Conclusion The CC genotype of IL-18 gene promoter -607 C/A polymorphism may contribute to the susceptibility of CHD in Chinese Han population,and allele C may be a genetic risk factor of CHD.

关键词

白细胞介素18/冠心病/单核苷酸多态性

Key words

Interleukin 18/Coronary heart disease/Single nucleotide polymorphism

分类

医药卫生

引用本文复制引用

朱名安,吕军,宋惠,刘兴晖,朱静..IL-18基因启动子-607C/A位点多态性与冠心病关系的研究[J].湖北医药学院学报,2011,30(5):471-474,479,5.

基金项目

湖北省教育厅重点项目(2003A012) (2003A012)

湖北医药学院学报

2096-708X

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