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晚期糖基化终末产物受体基因(RAGE)的-429 T/C和-374 T/A基因多态性并非斯洛文尼亚2型糖尿病患者群体冠状动脉疾病的风险因素。

The -429 T/C and -374 T/A gene polymorphisms of the receptor of advanced glycation end products gene (RAGE) are not risk factors for coronary artery disease in Slovene population with type 2 diabetes.

作者信息

Kirbis Janez, Milutinović Aleksandra, Steblovnik Klemen, Teran Natasa, Terzić Rifet, Zorc Marjeta

机构信息

Department of Cardiovascular Surgery, Medical Center Ljubljana, Ljubljana, Slovenia.

出版信息

Coll Antropol. 2004 Dec;28(2):611-6.

Abstract

Receptor for advanced glycation end products (RAGE) plays a role in atherosclerosis in diabetics. There are two functional polymorphisms in the promoter of the RAGE gene (-429T/C and -374T/A). The aim of this study was to look for a relationship between the -429T/C and the -374T/A gene polymorphisms of the RAGE gene and the development of coronary artery disease (CAD) in the Slovene population with type 2 diabetes of duration longer than 10 years. One hundred and sixty-eight subjects with diabetes and CAD were compared to 241 diabetic subjects without CAD. The -429T/C and the -374T/A RAGE genotype distributions in patients with CAD (-429T/C: CC: 3%, TC: 31%, TT: 66.0%; -374T/A:AA: 7.7%, TA: 48.2%, TT: 44.1%) were not significantly different from those in patients without CAD (-429 T/C: CC: 1.7%, TC: 26.1%, TT: 72.2%; -374T/A: AA: 11.2%, TA: 43.2%, TT: 45.6%). Our study failed to demonstrate an association between either the -429T/C or the -374T/A gene polymorphism of the RAGE gene and CAD in the Slovene population with type 2 diabetes of duration longer than 10 years.

摘要

晚期糖基化终末产物受体(RAGE)在糖尿病患者的动脉粥样硬化中起作用。RAGE基因启动子存在两种功能性多态性(-429T/C和-374T/A)。本研究旨在探寻RAGE基因的-429T/C和-374T/A基因多态性与病程超过10年的斯洛文尼亚2型糖尿病患者冠状动脉疾病(CAD)发生之间的关系。将168例患有糖尿病和CAD的受试者与241例无CAD的糖尿病受试者进行比较。CAD患者中-429T/C和-374T/A RAGE基因型分布(-429T/C:CC:3%,TC:31%,TT:66.0%;-374T/A:AA:7.7%,TA:48.2%,TT:44.1%)与无CAD患者(-429T/C:CC:1.7%,TC:26.1%,TT:72.2%;-374T/A:AA:11.2%,TA:43.2%,TT:45.6%)相比无显著差异。我们的研究未能证明在病程超过10年的斯洛文尼亚2型糖尿病患者中,RAGE基因的-429T/C或-374T/A基因多态性与CAD之间存在关联。

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