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汉族人血小板GP Ⅰ b HPA-2基因多态性与冠心病血瘀证的相关性研究 被引量:6

Research on the Association between the Platelet Membrane Glycoprotein Ⅰ b Polymorphism and Blood-Stasis Syndrome of Coronary Heart Disease in Han people
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摘要 目的观察GPⅠb HPA-2(Ko^b/Ko^a)基因多态性,在北京河北地区汉族人中各基因型的分布频率,分析该多态性与冠心病、冠心病血瘀证易感性的相关性。方法采用病例对照设计,筛选符合冠心病、血瘀证、健康人入选标准的110例冠心病血瘀证、102例冠心病非血瘀证患者及106例健康对照人群为研究对象,进行中医辨证分型、血瘀证计分,并记录冠脉造影病变支数,采用基因测序技术检测HPA-2基因多态性。结果GPⅠb HPA-2a/2a、HPA-2a/2b、HPA-2b/2b各占90.9%,8.8%和0.3%,所有入选病例中仅有1例表达HPA-2b/2b型;冠心病组和健康对照组、冠心病血瘀证组和冠心病非血瘀证组的基因型构成,冠心病患者不同病变支数基因型构成,冠心病血瘀证各基因型患者的血瘀证计分,各组间比较均无显著性差异(P>0.05)。以是否患冠心病为因变量的二分类Binary Logistic回归分析,校正年龄、性别、体重指数对冠心病的影响后,结果显示HPA-2多态位点基因型与冠心病发病无相关性。结论GPⅠb的HPA-2多态位点不是汉族人冠心病、冠心病血瘀证的独立危险因素。 Objective To learn the genotype distributions of HPA-2 (Kob/Ko^a) in Han people from Beijing and Hebei Province, and to study the association of the platelet glycoprotein Ⅰ b polymorphism with coronary heart disease (CHD), blood-stasis syndrome of CHD. Methods One hundred and ten patients with blood-stasis syndrome of coronary heart disease, 102 patients with the non-blood stasis syndrome of coronary heart disease and 106 healthy controls were enrolled in this case-control study. Differentiation of symptoms and signs for the classification of syndrome, scores of blood-stasis syndrome, and the number of occlusive coronary artery were performed or measured in all subjects. The genotypes of HPA-2 were determined by DNA sequencing technology. Results The frequencies of HPA-2 polymorphism were respectively 90.9%, 8.8% and 0.3%. There was only one carrier of HPA-2b/2b in our study, and the frequencies of HPA-2 polymorphism had no difference in CHD and healthy controls. The prevalence of HPA-2 genetic variants differ neither in blood-stasis syndrome of CHD and blood-stasis syndrome of CHD nor in CHD patients of different numbers of occlusive coronary artery. The scores of blood-stasis syndrome had no difference between different genotypes. Results were statistically evaluated with Binary Logistic Regression, which showed the HPA-2 polymorphism had no association with CHD. Conclusions The HPA-2 polymorphism of GP Ⅰ b is not the risk factor of CHD and blood-stasis syndrome of CHD in Han people.
出处 《中国分子心脏病学杂志》 CAS 2008年第4期196-202,共7页 Molecular Cardiology of China
基金 国家自然科学基金重大研究计划重点项目(90409021)
关键词 冠心病 血瘀证 血小板GP b 基因多态性 Coronary heart disease Blood-stasis syndrome Platelet membrane glycoprotein Ⅰ b Gene polymorphism
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