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颈动脉斑块及与炎症和内皮功能相关的候选基因与来自曼哈顿北部的西班牙裔人群有关。

Carotid plaque and candidate genes related to inflammation and endothelial function in Hispanics from northern Manhattan.

机构信息

Department of Neurology, University of Miami, Miller School of Medicine, PO Box 016960 (M-877), Miami, FL 33101, USA.

出版信息

Stroke. 2011 Apr;42(4):889-96. doi: 10.1161/STROKEAHA.110.591065. Epub 2011 Mar 10.

Abstract

BACKGROUND AND PURPOSE

The genetic influence on carotid atherosclerotic plaque is mostly unknown. This study examines the association between carotid plaque and single nucleotide polymorphisms in selected genes implicated in inflammation and endothelial function.

METHODS

A total of 43 genes (197 single nucleotide polymorphisms) involved in inflammation and endothelial function were interrogated in 287 Dominicans from the Northern Manhattan Study (mean age, 64±7 years; 58% women) who had undergone high-resolution B-mode ultrasound for examination of carotid plaque. Using an additive genetic model, multiple logistic regression analyses were conducted, a within-gene haplotype analysis was performed, and interactions between genes were examined. Results were validated in an independent set of 301 Dominicans.

RESULTS

Carotid plaque was present in 143 (47%) participants. Nine genes had at least 1 single nucleotide polymorphism associated (P≤0.01) with carotid plaque phenotypes: TNF, NOS2A, IL6R, TNFSF4, PPARA, IL1A, TLR4, ITGA2, and HABP2. Single nucleotide polymorphisms in TNFSF4, PPARA, TLR4, ITGA2, and HABP2 were also implicated with the same carotid phenotype in the validation analysis. Haplotype analysis revealed an additional gene of interest, VCAM1.

CONCLUSIONS

We report novel associations between variations in 10 genes involved in inflammation and endothelial function and carotid plaque phenotypes in a Dominican sample, with replication for 5 genes in an independent Dominican sample.

摘要

背景与目的

颈动脉粥样硬化斑块的遗传影响大多未知。本研究探讨了选定基因中与炎症和内皮功能相关的单核苷酸多态性与颈动脉斑块之间的关联。

方法

对 287 名来自北方曼哈顿研究(平均年龄 64±7 岁;58%为女性)的多米尼加人进行了高分辨率 B 型超声检查,以检查颈动脉斑块,共检测了 43 个参与炎症和内皮功能的基因(197 个单核苷酸多态性)。采用加性遗传模型,进行了多次逻辑回归分析,进行了基因内单倍型分析,并检查了基因之间的相互作用。在 301 名独立的多米尼加人中验证了结果。

结果

143 名(47%)参与者存在颈动脉斑块。有 9 个基因至少有 1 个单核苷酸多态性与颈动脉斑块表型相关(P≤0.01):TNF、NOS2A、IL6R、TNFSF4、PPARA、IL1A、TLR4、ITGA2 和 HABP2。在验证分析中,TNFSF4、PPARA、TLR4、ITGA2 和 HABP2 的单核苷酸多态性也与相同的颈动脉表型有关。单倍型分析显示另一个感兴趣的基因 VCAM1。

结论

我们报告了在多米尼加样本中,10 个参与炎症和内皮功能的基因中的变异与颈动脉斑块表型之间存在新的关联,在独立的多米尼加样本中对 5 个基因进行了复制。

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