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[载脂蛋白AI-CIII-AIV基因簇的DNA多态性与冠状动脉疾病]

[DNA polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster in coronary artery disease].

作者信息

Dan Q, Huang Y, Peng Z

机构信息

Cardiovascular Institute, Zhejiang Medical University, Hangzhou.

出版信息

Zhonghua Yi Xue Za Zhi. 1995 Oct;75(10):584-7, 637.

PMID:8697070
Abstract

Two polymorphic sites of the apolipoprotein AI (ApoAI) gene, PstI and SstI, were examined in a sample of 43 unrelated Chinese patients with coronary artery disease (CAD) and 60 unrelated healthy individuals. Allele frequencies were compared between patients and controls and their impact on lipid and oxygen free radicals metabolism were also studied. The frequencies of the uncommon P2 and S2 alleles in CAD cases were found as 0.14 and 0.22 respectively, which were significantly higher than 0.05 and 0.13 in controls. The more the number of vessel disease in CAD cases, the higher the frequencies of S2 alleles which were the highest in the group of 3 vessel diseases. Some serum lipid and oxygen free radicals levels differed between CAD cases of different genotypes. These data suggest that genetic variation in P2 and S2 alleles of APOAI gene may contribute to the development and extent of CAD in Chinese subjects.

摘要

在43名无亲缘关系的中国冠心病(CAD)患者和60名无亲缘关系的健康个体样本中,检测了载脂蛋白AI(ApoAI)基因的两个多态性位点PstI和SstI。比较了患者和对照组之间的等位基因频率,并研究了它们对脂质和氧自由基代谢的影响。发现CAD病例中罕见的P2和S2等位基因频率分别为0.14和0.22,显著高于对照组的0.05和0.13。CAD病例中血管疾病的数量越多,S2等位基因的频率越高,在三支血管疾病组中最高。不同基因型的CAD病例之间,一些血脂和氧自由基水平存在差异。这些数据表明,APOAI基因P2和S2等位基因的遗传变异可能与中国人群CAD的发生发展及严重程度有关。

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