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首页> 外文期刊>International Journal of Medical Sciences >Scavenger Receptor Class B Type 1 Gene rs5888 Single Nucleotide Polymorphism and the Risk of Coronary Artery Disease and Ischemic Stroke: A Case-Control Study
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Scavenger Receptor Class B Type 1 Gene rs5888 Single Nucleotide Polymorphism and the Risk of Coronary Artery Disease and Ischemic Stroke: A Case-Control Study

机译:清除剂受体B类1型基因rs5888单核苷酸多态性与冠状动脉疾病和缺血性中风的风险:病例对照研究

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Background: Our previous studies have showed that the rs5888 single nucleotide polymorphism (SNP) in Scavenger receptor class B type 1 (SCARB1) gene is associated with serum lipid levels in the general Chinese populations. The present study was undertaken to detect the associations between rs5888 SNP and the risk of coronary artery disease (CAD) and ischemic stroke (IS). Methods: A total of 1,716 unrelated subjects (CAD, 601; IS, 533; and healthy controls, 582) were included in this study. Genotyping of the rs5888 SNP were determined by polymerase chain reaction and restriction fragment length polymorphism. Results: The genotypic frequencies of SCARB1 rs5888 SNP were different between CAD patients and controls, the subjects with TT genotype had high risk of CAD (OR = 1.76, P = 0.038 for TT vs. CC; and OR = 1.75, P = 0.036 for TT vs. CC/CT). There was no significant association between genotypes and the risk of IS. Further analysis showed that the subjects with TT genotype in the total population had lower levels of high-density lipoprotein cholesterol than the subjects with CC/CT genotypes (P P 0.05 for each). Conclusions: The present study suggests that the SCARB1 rs5888 SNP influences serum lipid levels, and is associated with the risk of CAD.
机译:背景:我们以前的研究表明,在普通华人人群中,清道夫受体B类1型(SCARB1)基因中的rs5888单核苷酸多态性(SNP)与血清脂质水平相关。本研究旨在检测rs5888 SNP与冠状动脉疾病(CAD)和缺血性中风(IS)的风险之间的关联。方法:本研究共纳入1,716名无关受试者(CAD,601; IS,533;健康对照组,582)。 rs5888 SNP的基因分型通过聚合酶链反应和限制性片段长度多态性确定。结果:CAD患者和对照组之间SCARB1 rs5888 SNP的基因型频率不同,TT基因型受试者有较高的CAD风险(TT vs. CC的OR = 1.76,P = 0.038; OR = 1.75,P = 0.036)。 TT与CC / CT)。基因型与IS风险之间没有显着关联。进一步的分析显示,总人口中具有TT基因型的受试者的高密度脂蛋白胆固醇水平低于CC / CT基因型的受试者(每项P P 0.05)。结论:本研究表明SCARB1 rs5888 SNP影响血清脂质水平,并与CAD风险相关。

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