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[早发冠心病患者载脂蛋白A5基因多态性研究]

[Study on polymorphism in the apolipoprotein A5 gene in patients with premature coronary heart disease].

作者信息

Yu Yang, Xue Lin, Zhao Chun Yu

机构信息

Department of Cardiology, Peking University First Hospital, Beijing 100034, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2007 Dec 18;39(6):576-80.

Abstract

OBJECTIVE

To investigate the association between the apolipoprotein A5(APOA5) -1131T/C polymorphism and premature coronary heart disease in northern Chinese Han population.

METHODS

Using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and polyacrylamide gel electrophoresis (PAGE), we analyzed the genotype and allele distribution in 140 patients with premature coronary heart disease diagnosed by coronary angiography and 156 healthy controls. The levels of serum lipid profiles were also studied by biochemical methods.

RESULTS

The allele frequency of APOA5-1131T/C polymorphism in the premature coronary heart disease group was significantly higher (43.2% vs. 33.0%, P=0.011) than that in the control group. Compared with TT homozygotes, CC homozygotes exhibited a 2.809-fold (95% CI 1.331-5.927) increased risk of developing premature coronary heart disease. Logistic regression analysis found that this correlation was independent of sex, age, body mass index (BMI), smoking history as well as serum total cholesterol(TC), high density lipoprotein cholesterol (HDL-C) and low density lipoprotein cholesterol (LDL-C) levels; In premature coronary heart disease group, the triglyceride(TG) level in CC homozygotes was significantly higher than those in TC heterozygotes or TT homozygotes.

CONCLUSION

The APOA5-1131T/C polymorphism has influence on serum TG level, and the APOA5-1131C allele is associated with the development of premature coronary heart disease in northern Chinese Han population.

摘要

目的

探讨载脂蛋白A5(APOA5)-1131T/C基因多态性与中国北方汉族人群早发冠心病的关系。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和聚丙烯酰胺凝胶电泳(PAGE)技术,分析140例经冠状动脉造影确诊的早发冠心病患者和156例健康对照者的基因型和等位基因分布。同时采用生化方法检测血脂水平。

结果

早发冠心病组APOA5-1131T/C基因多态性的等位基因频率显著高于对照组(43.2%比33.0%,P=0.011)。与TT纯合子相比,CC纯合子患早发冠心病的风险增加2.809倍(95%可信区间1.331-5.927)。Logistic回归分析发现,这种相关性独立于性别、年龄、体重指数(BMI)、吸烟史以及血清总胆固醇(TC)、高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C)水平;在早发冠心病组中,CC纯合子的甘油三酯(TG)水平显著高于TC杂合子或TT纯合子。

结论

APOA5-1131T/C基因多态性对血清TG水平有影响,APOA5-1131C等位基因与中国北方汉族人群早发冠心病的发生有关。

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