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在芬兰经血管造影证实患有冠状动脉疾病的患者中,载脂蛋白B基因3'高变区等位基因与冠状动脉疾病之间无关联。

Lack of association between the apolipoprotein B gene 3' hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease.

作者信息

Heliö T, Palotie A, Tötterman K J, Ott J, Kauppinen-Mäkelin R, Tikkanen M J

机构信息

First Department of Medicine, University of Helsinki, Finland.

出版信息

J Intern Med. 1992 Jan;231(1):49-57. doi: 10.1111/j.1365-2796.1992.tb00498.x.

Abstract

Previous studies have suggested that some apolipoprotein B (apoB) 3' variable number of tandem repeats (3'VNTR) locus alleles are associated with coronary artery disease (CAD). We examined the possible association between the apoB 3'VNTR alleles and CAD in 387 Finnish subjects. Using the polymerase chain reaction and polyacrylamide gel electrophoresis, the 3'VNTR genotype was determined in 187 individuals with severe CAD confirmed by coronary angiography (patients), in 121 individuals with normal coronary angiograms (controls), and in 79 apparently healthy subjects (normals). In contrast to previous reports from other populations, the larger apoB 3'VNTR alleles were not significantly more frequent among CAD patients than among controls or normals. In addition, there was no significant association between the 3'VNTR alleles and serum lipid levels in this Finnish population.

摘要

以往的研究表明,一些载脂蛋白B(apoB)3'端串联重复序列(3'VNTR)位点的等位基因与冠状动脉疾病(CAD)有关。我们在387名芬兰受试者中研究了apoB 3'VNTR等位基因与CAD之间的可能关联。采用聚合酶链反应和聚丙烯酰胺凝胶电泳技术,在187例经冠状动脉造影确诊为严重CAD的个体(患者)、121例冠状动脉造影正常的个体(对照)以及79例明显健康的受试者(正常人)中确定了3'VNTR基因型。与其他人群的既往报道不同,在CAD患者中,较大的apoB 3'VNTR等位基因的频率并不显著高于对照组或正常组。此外,在这个芬兰人群中,3'VNTR等位基因与血脂水平之间没有显著关联。

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