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Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.常见止血和炎症基因变异与心血管健康研究中老年人群的静脉血栓形成。
J Thromb Haemost. 2009 Sep;7(9):1499-505. doi: 10.1111/j.1538-7836.2009.03522.x. Epub 2009 Jun 22.
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Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study.颈动脉内膜中层厚度的节段特异性遗传效应:北曼哈顿研究
Stroke. 2008 Dec;39(12):3159-65. doi: 10.1161/STROKEAHA.108.522789. Epub 2008 Sep 11.
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Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke.胆固醇酯转运蛋白、白细胞介素-8、过氧化物酶体增殖物激活受体α和Toll样受体4基因变异与非致死性心肌梗死和缺血性中风发病风险
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Carotid plaque, a subclinical precursor of vascular events: the Northern Manhattan Study.颈动脉斑块,血管事件的亚临床先兆:北曼哈顿研究
Neurology. 2008 Apr 1;70(14):1200-7. doi: 10.1212/01.wnl.0000303969.63165.34. Epub 2008 Mar 19.
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Association between PPARalpha gene polymorphisms and myocardial infarction.过氧化物酶体增殖物激活受体α(PPARα)基因多态性与心肌梗死之间的关联。
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Factor VII-activating protease (FSAP): vascular functions and role in atherosclerosis.凝血因子VII激活蛋白酶(FSAP):血管功能及其在动脉粥样硬化中的作用
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Toll-like receptor 4 gene (Asp299Gly) polymorphism associates with carotid artery elasticity. The cardiovascular risk in young Finns study.Toll样受体4基因(Asp299Gly)多态性与颈动脉弹性相关。芬兰年轻人心血管风险研究。
Atherosclerosis. 2008 May;198(1):152-9. doi: 10.1016/j.atherosclerosis.2007.09.024. Epub 2007 Nov 9.
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Association of integrin alpha2 gene variants with ischemic stroke.整合素α2基因变异与缺血性中风的关联。
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Toll receptor polymorphisms and carotid artery intima-media thickness.Toll受体多态性与颈动脉内膜中层厚度
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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.

DOI:10.1161/STROKEAHA.110.591065
PMID:21393601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3116444/
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。