急性冠状动脉综合征患者血小板内皮细胞粘附分子1基因多态性分析
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The Analysis of Platelet Endothelial Cell Adhesion Molecule-1 Gene Polymorphism in the Patients of Acute Coronary Syndrome
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    目的为观察血小板内皮细胞粘附分子1基因多态性与急性冠状动脉综合征的关系。方法117例急性冠状动脉综合征患者作为病例组,根据年龄和性别进行1∶1匹配,经冠状动脉造影证实完全正常冠状动脉的患者作为对照组。利用多聚酶链反应-限制性内切酶法分析基因型,部分样本基因型经基因测序核实。结果血小板内皮细胞粘附分子1的125Leu和563Ser等位基因频率在病例组中显著升高(病例组∶对照组分别为51.7%∶39.7%和54.3%∶42.3%,均p<0.05);基因型125Leu/Leu+125Leu/Val和563Ser/Ser+563Ser/Asn病例组较对照组高(p<0.05),回归分析后发现Leu125Leu+Leu125Val基因型与急性冠状动脉综合征有相关(p<0.05);两个等位基因有紧密连锁(D’=0.896);冠状动脉病变数目与基因多态性无相关性(p>0.05);急性心肌梗死和不稳定型心绞痛患者基因分布无显著相关性(p>0.05)。结论第3外显子基因多态性可能与急性冠状动脉综合征发病过程中不稳定班块有关。

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    Aim To investigate the association of platelet endothelial cell adhesion molecule 1 gene polymorphisms with acute coronary syndrome.Methods We analyzed two single nucleotide polymorphisms of platelet endothelial cell adhesion molecule 1 gene Leu125Val and Ser563Asn in 117 angiographically documented patients with acute coronary syndrome and 117 age-and sex-matched controls in the Chinese population,using a polymerase chain reaction-restriction fragment length polymorphism strategy.Some samples were verified by direct sequencing.Results we found that two polymorphisms were in linkage disequilibrium with each other(D'=0.896)and that frequencies of 125Leu1 and 563Ser alleles were significantly increased in patients compared with controls(51.7% vs 39.7%,p<0.05;54.3% vs 42.3%,p<0.05,respectively).The frequencies of genotypes for 125Leu/Leu+ 125Leu/Val and 563Ser/Ser+ 563Ser/Asn were also significantly increased in the patients(p<0.05).In addition,there were no significant difference in patients among different vessel disease and between acute myocardial infarction and unstable angina.Conclusion platelet endothelial cell adhesion molecule 1 gene polymorphism may be a genetic risk factor for acute coronary syndrome.

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全锦花,张新超,蔡剑平,何青,许锋,戴大鹏.急性冠状动脉综合征患者血小板内皮细胞粘附分子1基因多态性分析[J].中国动脉硬化杂志,2007,15(2):120~124.

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  • 收稿日期:2006-06-16
  • 最后修改日期:2007-02-03
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