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SERPINA9基因变异与颈动脉粥样硬化的关联:社区动脉粥样硬化风险(ARIC)颈动脉MRI研究

Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study.

作者信息

Tang Weihong, Morrison Alanna, Wasserman Bruce A, Folsom Aaron R, Sun Wei, Campbell Stephen, Kao W H Linda, Boerwinkle Eric

机构信息

Division of Epidemiology and Community Health, School of Public Health, University of Minnesota Minneapolis, MN, USA.

出版信息

Int J Mol Epidemiol Genet. 2013 Nov 28;4(4):258-67. eCollection 2013.

Abstract

The SNP rs11628722 in the SERPINA9 gene was previously associated with incident ischemic stroke in the Atherosclerosis Risk in Communities (ARIC) study. Centerin, the protein encoded by SERPINA9, is involved in maturation and maintenance of naïve B cells, which play a role in atherogenesis. We investigated whether 21 tag SNPs in the SERPINA9 gene are associated with features of carotid artery atherosclerotic plaque measured by magnetic resonance imaging (MRI). Carotid MRI data were obtained from 1,282 European Americans and 341 African Americans of the ARIC Carotid MRI study, which recruited participants from ARIC by a stratified sampling plan that over-sampled participants with carotid intima-media thickening. Five MRI measures, focused on carotid wall volume, wall thickness, and lipid core, were analyzed. Genetic associations between the MRI measurements and each of the 21 SNPs were analyzed in linear regression models with adjustment for sample weights and traditional risk factors. Rs11628722 was tested a priori. In African Americans, rs11628722 was significantly associated with carotid wall volume (p < 0.05). Among the other 20 SNPs, adjusted for multiple testing, rs4905204, which encodes an Ala to Val amino acid change, was significantly associated with maximum wall thickness (p < 0.000625) and suggestively associated with total wall volume (p < 0.0026) in European Americans. In conclusion, SNPs in the SERPINA9 gene showed race-specific associations with characteristics of carotid atherosclerotic plaques. Replications in other populations are needed to validate findings of this study and to establish the SERPINA9 gene as a candidate in the etiology of carotid atherosclerosis.

摘要

在社区动脉粥样硬化风险(ARIC)研究中,SERPINA9基因中的单核苷酸多态性(SNP)rs11628722先前与缺血性卒中发病相关。SERPINA9基因编码的蛋白Centerin参与未成熟B细胞的成熟和维持,而未成熟B细胞在动脉粥样硬化形成中起作用。我们研究了SERPINA9基因中的21个标签SNP是否与通过磁共振成像(MRI)测量的颈动脉粥样硬化斑块特征相关。颈动脉MRI数据来自ARIC颈动脉MRI研究中的1282名欧裔美国人和341名非裔美国人,该研究通过分层抽样计划从ARIC招募参与者,对颈动脉内膜中层增厚的参与者进行了过度抽样。分析了五项聚焦于颈动脉壁体积、壁厚和脂质核心的MRI测量指标。在对样本权重和传统风险因素进行校正的线性回归模型中,分析了MRI测量指标与21个SNP中每一个的遗传关联。对rs11628722进行了预先检验。在非裔美国人中,rs11628722与颈动脉壁体积显著相关(p<0.05)。在其他20个SNP中,经多重检验校正后,编码丙氨酸到缬氨酸氨基酸变化的rs4905204在欧裔美国人中与最大壁厚显著相关(p<0.000625),并与总壁体积有提示性关联(p<0.0026)。总之,SERPINA9基因中的SNP与颈动脉粥样硬化斑块特征存在种族特异性关联。需要在其他人群中进行重复研究,以验证本研究结果,并将SERPINA9基因确立为颈动脉粥样硬化病因学的候选基因。

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