CX3CR1基因多态性与冠心病的相关性
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A Study on Association of Fractalkine Receptor CX3CR1 Gene Polymorphism to Coronary Heart Disease
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    摘要:

    目的研究Fractalkine受体CX3CR1基因多态性(249V/I和280T/M)与冠心病的相关性。方法应用聚合酶链反应限制片长多态性方法对139例冠心病患者和90例对照者的CX3CR1基因多态性进行分析,比较CX3CR1基因多态性在两组之间的差异性。结果等位基因I249在对照组中的分布频率明显高于冠心病组(P><0.05);冠心病组280T/M基因型和等位基因频率分布与对照组比较无显著性差异(P>0.05)。结论Fractalkine受体CX3CR1等位基因I249变异可能与冠心病的发病危险性下降有关,CX3CR1基因多态性与中国南方汉族人群冠心病的发生存在相关性。

    Abstract:

    Aim To investigate the relationship between Fractalkine receptor CX3CR1 gene polymorphism and coronary heart disease(CHD). Methods By polymerase chain reaction and restriction fragment length polymorphism(PCR-RFLP),CX3CR1 gene polymorphism was analyzed in 139 CHD patients and 90 control individuals,and the distribution of CX3CR1 genotype was compared in CHD group and control group. Results The proportion of I249 allele was higher in control group than in CHD group(24.4% and 9.4%,P><0.05).There were no significant differences in 280T/M genotype frequencies and allele frequencies between CHD group and control group(P>0.05). Conclusion The I249 allele of the Fractalkine receptor CX3CR1 gene may be associated with a reduced risk of coronary heart disease,the CX3CR1 gene polymorphism is associated with CHD in Han nationality of South China.

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肖宏凯,金莉子,谢桂庭,陈剑,陈筱潮,徐明彤. CX3CR1基因多态性与冠心病的相关性[J].中国动脉硬化杂志,2010,18(12):993~995.

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  • 收稿日期:2010-07-30
  • 最后修改日期:2010-12-07
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