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白细胞介素-10启动子多态性在严重主-髂动脉闭塞性疾病发生中的作用

Role of IL-10 promoter polymorphisms in the development of severe aorto-iliac occlusive disease.

作者信息

Blanco Estrella, Moñux Guillermo, Mas Ana, Serrano Francisco J, de la Concha Emilio G, Urcelay Elena

机构信息

Unit of Angiology and Vascular Surgery, Hospital Universitario de Guadalajara, Guadalajara, Spain.

出版信息

Hum Immunol. 2008 Oct;69(10):651-4. doi: 10.1016/j.humimm.2008.07.005. Epub 2008 Aug 12.

Abstract

Aortic severe occlusive disease (ASO) is a peripheral manifestation of atherosclerosis with an inflammatory component. Interleukin (IL)-10 is an anti-inflammatory cytokine that plays a key role in the development of atherosclerosis, promoting the stability of the atherosclerotic plaque. Several polymorphisms within the 5' region of the IL-10 gene have been related to altered transcriptional activity and protein levels. We aimed at studying two microsatellites, IL-10R and IL-10G, at -4 and -1.2 Kb, and three single nucleotide polymorphisms at positions -1082A/G, -819C/T and -592C/A in a collection of 94 ASO patients and 519 ethnically matched controls. Our results show that the IL-10 proximal promoter haplotype IL-10G*11/ -1082G/ -819C/ -592C is more frequent in ASO patients than in controls (28.7% vs 16% p = 0.003; OR = 2.12). Therefore, our data suggest a role of the IL-10 gene on ASO susceptibility.

摘要

主动脉严重闭塞性疾病(ASO)是动脉粥样硬化的一种外周表现形式,具有炎症成分。白细胞介素(IL)-10是一种抗炎细胞因子,在动脉粥样硬化的发展过程中起关键作用,可促进动脉粥样硬化斑块的稳定性。IL-10基因5'区域内的几种多态性与转录活性和蛋白质水平的改变有关。我们旨在研究94例ASO患者和519例种族匹配的对照人群中位于-4和-1.2 kb处的两个微卫星IL-10R和IL-10G,以及位于-1082A/G、-819C/T和-592C/A位置的三个单核苷酸多态性。我们的结果显示,ASO患者中IL-10近端启动子单倍型IL-10G*11 / -1082G / -819C / -592C的频率高于对照组(28.7%对16%,p = 0.003;OR = 2.12)。因此,我们的数据表明IL-10基因在ASO易感性中起作用。

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