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MMP2 基因变异与纤维帽厚度的测量指标相关:社区动脉粥样硬化风险研究的颈动脉 MRI 研究。

MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study.

机构信息

University of Texas Health Science Center School of Public Health, Human Genetics Center, 1200 Hermann Pressler, Houston, TX 77030, United States.

出版信息

Atherosclerosis. 2010 May;210(1):188-93. doi: 10.1016/j.atherosclerosis.2009.12.006. Epub 2009 Dec 11.

Abstract

OBJECTIVE

Genetic variation in matrix metalloproteinase (MMP) promoter regions alter the transcriptional activity of MMPs and has been consistently associated with CHD, presumably through plaque degradation and remodeling. We examined the association of MMP promoter variation with multiple plaque characteristics measured by gadolinium-enhanced MRI among 1700 participants in the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study.

METHODS

For the analyses presented here, 1700 participants of the biracial ARIC Carotid MRI Study ( approximately 1000 participants with thick carotid artery walls and approximately 700 randomly sampled participants) were evaluated for associations of MMP genetic variation with multiple plaque characteristics, including carotid artery wall thickness, lipid core and fibrous cap measures. MRI studies were performed on a 1.5T scanner equipped with a bilateral 4-element phased array carotid coil.

RESULTS

Fifty-one percent of the participants were female, 77% white, 23% African American, and the mean age was 70 years. MMP2 C-1306T variant genotypes (CT+TT) were significantly associated with higher cap thickness measures, but not with wall thickness or lipid core measures. Individuals with the CC genotype had approximately 0.1mm thinner cap thickness compared to those carrying a T allele (P=0.02).

CONCLUSION

Genetic variation within the MMP2 promoter region was associated with cap thickness and therefore may influence the role of MMP2 in plaque vulnerability.

摘要

目的

基质金属蛋白酶(MMP)启动子区域的遗传变异改变了 MMP 的转录活性,并与 CHD 密切相关,可能是通过斑块降解和重塑。我们在动脉粥样硬化风险社区(ARIC)颈动脉 MRI 研究的 1700 名参与者中,通过钆增强 MRI 测量了多种斑块特征,研究了 MMP 启动子变异与这些特征之间的关系。

方法

在本研究的分析中,对 1700 名 ARIC 颈动脉 MRI 研究的双种族参与者(约 1000 名颈动脉壁增厚的参与者和约 700 名随机抽样的参与者)进行了 MMP 遗传变异与多种斑块特征的相关性分析,包括颈动脉壁厚度、脂质核心和纤维帽测量。MRI 研究在配备双侧 4 元件相控阵颈动脉线圈的 1.5T 扫描仪上进行。

结果

51%的参与者为女性,77%为白人,23%为非裔美国人,平均年龄为 70 岁。MMP2 C-1306T 变体基因型(CT+TT)与较厚的帽厚度测量值显著相关,但与壁厚度或脂质核心测量值无关。与携带 T 等位基因的个体相比,CC 基因型的个体帽厚度约薄 0.1mm(P=0.02)。

结论

MMP2 启动子区域内的遗传变异与帽厚度相关,因此可能影响 MMP2 在斑块脆弱性中的作用。

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