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[CD14启动子区域C-159T多态性与冠心病的关联]

[Association of C-159T polymorphism in promoter region of CD14 and coronary heart disease].

作者信息

Li Yan, Xiong Xiao-quan, Zhang Ping-an, Ming Kai-hua

机构信息

Department of Laboratory Science, Renmin Hospital, Wuhan University, Wuhan, Hubei, P. R. China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):687-90.

Abstract

OBJECTIVE

To investigate the distribution of CD14 promoter gene -159(C>T) polymorphism in Hubei Han population of China and analyze the association of CD14 polymorphisms with coronary heart disease (CHD).

METHODS

Genotypes of CD14 were typed in 162 CHD patients and 196 controls by polymerase chain reaction-restriction fragment length polymorphism. Selected coronary angiography was performed in 162 CHD patients.

RESULTS

CD14 promoter -159 genotype frequencies of CC, CT and TT were 27.4%, 45.6%, 27.0% and 14.8%, 46.5%, 38.7% in normal control group and CHD group respectively. Genotype distribution was in accordance with Hardy-Weinberg equilibrium. There existed statistically significant difference in frequencies of allele and genotype in CD14 C-159T polymorphism between CHD group and control group (Genotype: Chi2=0.654, P < 0.05, CT vs CC, OR=1.245, 95%CI: 1.001-1.473, TT vs CC, OR=2.374, 95%CI 2.012-2.649; Allele: Chi2=0.547, P < 0.05, T vs C, Chi2=0.547, P < 0.05, OR=3.105, 95%CI: 2.493-3.539). The distributions of allele and genotype in CD14 -159(C>T) were of statistically significant difference between non-myocardial infarction subgroup and myocardial infarction subgroup (Genotype: Chi2=0.782, P < 0.05, CT vs CC, OR=2.375, 95%CI: 2.017-2.689, TT vs CC, OR=3.459, 95%CI: 3.003-3.846. Allele: Chi2=2.374, P < 0.05, T vs C, Chi2=2.374, P < 0.05, OR=4.011, 95%CI: 3.814-4.279). However, no statistically significant difference was found among the subgroups of oneìtwo and three stenosed vessels.

CONCLUSION

The T allele of the C-159T polymorphism of CD14 gene may be a risk factor for myocardial infarction.

摘要

目的

研究中国湖北汉族人群CD14启动子基因-159(C>T)多态性的分布情况,并分析CD14基因多态性与冠心病(CHD)的相关性。

方法

采用聚合酶链反应-限制性片段长度多态性技术对162例冠心病患者和196例对照者的CD14基因型进行分型。对162例冠心病患者进行选择性冠状动脉造影检查。

结果

正常对照组和冠心病组CD14启动子-159基因型CC、CT和TT的频率分别为27.4%、45.6%、27.0%和14.8%、46.5%、38.7%。基因型分布符合Hardy-Weinberg平衡。冠心病组与对照组CD14 C-159T多态性的等位基因和基因型频率存在统计学差异(基因型:χ2=0.654,P<0.05,CT与CC比较,OR=1.245,95%CI:1.001-1.473,TT与CC比较,OR=2.374,95%CI 2.012-2.649;等位基因:χ2=0.547,P<0.05,T与C比较,χ2=0.547,P<0.05,OR=3.105,95%CI:2.493-3.539)。CD14 -159(C>T)等位基因和基因型在非心肌梗死亚组与心肌梗死亚组之间的分布存在统计学差异(基因型:χ2=0.782,P<0.05,CT与CC比较,OR=2.375,95%CI:2.017-2.689,TT与CC比较,OR=3.459,95%CI:3.003-3.846。等位基因:χ2=2.374,P<0.05,T与C比较,χ2=2.374,P<0.05,OR=4.011,95%CI:3.814-4.279)。然而,在单支、双支和三支血管狭窄亚组之间未发现统计学差异。

结论

CD14基因C-159T多态性的T等位基因可能是心肌梗死的危险因素。

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