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LURIC队列研究中白细胞介素-6基因G(-174)C启动子多态性:与血浆白细胞介素-6、冠状动脉疾病及心肌梗死无关联

The interleukin-6 G(-174)C promoter polymorphism in the LURIC cohort: no association with plasma interleukin-6, coronary artery disease, and myocardial infarction.

作者信息

Nauck Markus, Winkelmann Bernhard R, Hoffmann Michael M, Böhm Bernhard O, Wieland Heinrich, März Winfried

机构信息

Department of Medicine, University Hospital, Hugstetter Strasse 55, 79106 Freiburg, Germany.

出版信息

J Mol Med (Berl). 2002 Aug;80(8):507-13. doi: 10.1007/s00109-002-0354-2. Epub 2002 Jun 21.

DOI:10.1007/s00109-002-0354-2
PMID:12185451
Abstract

IL-6 plasma levels are predictive of major cardiovascular events. Recently a G/C polymorphism at position -174 in the promoter of the IL-6 gene has been associated with differences in both the IL-6 transcription rate in vitro and IL-6 levels in vivo. We examined the association of this polymorphism with coronary artery disease (CAD) and previous myocardial infarction (MI) in 2559 patients with angiographically documented CAD with ( n=1365) and without ( n=1194) MI and in a control group of 729 individuals in whom CAD had been ruled out angiographically. Assuming dominant or recessive modes of inheritance, carriers of the G allele had odds ratios of 0.98 (95% CI 0.79 - 1.20) and 0.96 (95% CI 0.80 - 1.14), respectively, for CAD, and almost identical ones for previous MI. In subgroups stratified for low cardiovascular risk, the IL-6 promoter polymorphism was also not related to the risk of CAD or MI. In addition, the plasma concentration of IL-6 did not differ between groups with different IL-6 genotypes in 942 randomly selected individuals. We conclude that the IL-6 G(-174)C polymorphism is not associated with the risk of CAD or MI and does not contribute to cardiovascular risk stratification.

摘要

白细胞介素-6(IL-6)的血浆水平可预测重大心血管事件。最近,IL-6基因启动子-174位的G/C多态性与体外IL-6转录率及体内IL-6水平的差异相关。我们在2559例经血管造影证实患有冠心病(CAD)的患者中研究了这种多态性与冠心病及既往心肌梗死(MI)的关系,其中有MI的患者1365例,无MI的患者1194例,并与729例经血管造影排除CAD的个体组成的对照组进行比较。假设遗传方式为显性或隐性,对于CAD,G等位基因携带者的比值比分别为0.98(95%可信区间0.79 - 1.20)和0.96(95%可信区间0.80 - 1.14),对于既往MI,比值比几乎相同。在按低心血管风险分层的亚组中,IL-6启动子多态性也与CAD或MI的风险无关。此外,在942例随机选择的个体中,不同IL-6基因型组之间的IL-6血浆浓度无差异。我们得出结论,IL-6 G(-174)C多态性与CAD或MI的风险无关,对心血管风险分层无贡献。

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