首页> 外文期刊>Cardiovascular Diabetology >Association of arterial stiffness with single nucleotide polymorphism rs1333049 and metabolic risk factors
【24h】

Association of arterial stiffness with single nucleotide polymorphism rs1333049 and metabolic risk factors

机译:动脉僵硬度与单核苷酸多态性rs1333049和代谢危险因素的关联

获取原文
       

摘要

Background Increased arterial stiffness is a cardiovascular outcome of metabolic syndrome (MetS). The chromosome 9p21 locus has been identified as a major locus for risk of coronary artery disease (CAD). The single nucleotide polymorphism (SNP), rs1333049 on chromosome 9p21.3 has been strongly associated with CAD and myocardial infarction. Increased arterial stiffness could be the link between the 9p21 polymorphism and increased cardiovascular risk. Since the impact of a genetic polymorphism on arterial stiffness especially in Asian populations has not been well defined, we aimed to investigate the association of arterial stiffness with rs 1333049 variant on chromosome 9p21.3 in Thai subjects with and without MetS risk factors. Methods A total of 208 Thai subjects, aged 35–75 years, 135 with and 73 without MetS, according to IDF and NCEP-ATPIII criteria, were included in this study. Aortic-femoral pulse wave velocity (afPWV), brachial-ankle pulse wave velocity (baPWV) and aortic ankle pulse wave velocity (aaPWV) were measured and used as markers of arterial stiffness. The chromosome 9p21.3 locus, represented by the rs 1333049 variant and blood biochemistry were evaluated. Results Arterial stiffness was elevated in subjects with MetS when compared with nonMetS subjects. PWV, especially afPWV increased progressively with increasing number of MetS risk factors (r = 0.322, P Conclusions Our findings demonstrate for the first time that arterial stiffness is associated with genetic polymorphism in 9p21 and metabolic risk factors in a Thai population.
机译:背景技术动脉僵硬度增加是代谢综合征(MetS)的心血管结果。 9p21染色体位点已被确定为冠心病(CAD)风险的主要位点。 9p21.3染色体上的单核苷酸多态性(SNP)rs1333049与CAD和心肌梗塞密切相关。动脉僵硬度增加可能是9p21多态性与心血管风险增加之间的联系。由于尚未明确定义遗传多态性对动脉僵硬度的影响,尤其是在亚洲人群中,因此我们旨在研究具有和不具有MetS危险因素的泰国受试者中,动脉僵硬度与rs 1333049变异体在9p21.3染色体上的关联。方法根据IDF和NCEP-ATPIII标准,总共包括208名泰国受试者,年龄35-75岁,有MetS的135名和73名无MetS的受试者。测量主股脉搏波速度(afPWV),臂踝脉搏波速度(baPWV)和主动脉踝脉搏波速度(aaPWV),并将其用作动脉僵硬度的标志物。评价了以rs 1333049变体为代表的染色体9p21.3基因座和血液生物化学。结果与非MetS受试者相比,MetS受试者的动脉僵硬度升高。 PWV,尤其是afPWV随着MetS危险因素数量的增加而逐渐增加(r = 0.322,P结论)我们的发现首次证明了动脉僵硬度与泰国人群9p21基因多态性和代谢危险因素相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号