西孟加拉邦人群PCSK9/Eam1104I基因多态性与血脂浓度和冠心病的相关性研究

S. Maiti, Pranamita Biswas, S. Banerjee, N. Jana
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引用次数: 1

摘要

冠状动脉疾病(CAD)被认为是发达国家死亡的主要原因。由于胆固醇和脂肪的沉积,斑块在心脏动脉内壁形成,导致心脏血管变窄,降低血液流入心脏的速度。蛋白转化酶枯草杆菌样keexin 9型(PCSK9)是CAD发病过程中调控脂蛋白滞留途径的候选基因之一。它是一种新发现的丝氨酸蛋白酶,通过介导LDL受体(LDLR)在LDL- c稳态中起关键作用。低密度脂蛋白受体通过转录后机制分解,诱导空腹状态下极低密度脂蛋白的产生。本研究的目的是调查155名CAD患者和102名年龄匹配的健康对照者PCSK9基因单核苷酸多态性(SNP)的频率。分析血清脂质包括总胆固醇(TC)、甘油三酯(TG)、HDL、LDL和VLDL。PCR-RFLP分析了PCSK9中携带Eam 1104I酶切位点的基因型区域。基因考虑患者与对照组血清TC、TG、HDL-C、LDL-C、VLDL-C水平差异有统计学意义(P<0.001, <0.0001)。在CAD患者中,G等位基因频率小于A等位基因频率。G等位基因负责降低LDL: HDL比率,这表明它对西孟加拉邦人群冠心病的发生有保护作用。人体循环系统或心血管系统通过各种血管将血液和其他必需营养素循环到全身。冠状动脉疾病(CAD)是与该系统相关的最常见疾病之一[1]。根据世界卫生组织的一份报告,每年有730万人死于冠心病,约占全球死亡人数的13%。印度的情况是最糟糕的,使其成为“世界冠心病之都”。这导致对额外工具的需求不断增长,以帮助临床医生识别有CAD风险的“脆弱”患者。在线阅读本文快速响应代码网站:
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Study of the Association of PCSK9/Eam1104I Gene Polymorphism with Plasma Lipid Concentration and CAD in West Bengal Population
Coronary artery disease (CAD) is suspected as a leading cause of mortality in developed countries. Due to cholesterol and fat deposit plaque is forming into the inner walls of the arteries of the heart, which leads to narrowing of blood vessels of heart and reduce the blood flow rate into heart. Proprotein convertase subtilisin-like kexin type 9 (PCSK9) is one of the candidate gene that regulate lipoprotein retention pathway of CAD development. It is a newly discovered serine protease that plays a key role in LDL-C homeostasis by mediating LDL receptor (LDLR). The LDL receptor is breakdown through a post transcriptional mechanism and induces the production of very low-density lipoprotein in the fasting state. The aim of this study was to investigate the frequency of single nucleotide polymorphism (SNP) of PCSK9 gene of 155 CAD patients and 102 ages matched healthy controls. Serum lipids including total cholesterol (TC), triglycerides (TG), HDL, LDL, and VLDL were analyzed. PCR-RFLP analysis was carried out to genotype regions carrying Eam 1104I restriction site in the PCSK9. Gene considering significant difference in serum TC, TG, HDL-C, LDL-C and VLDL-C levels (P<0.001, <0.0001) of patients and control samples. In CAD patients, G allele frequency is less than A allele frequency. G allele is responsible for decreasing the LDL: HDL ratio which shows evidence in having its protecting effect on the occurrence of CAD in West Bengal Population. Key-wordsCAD, PCSK9, SNP, Eam1104I, Polymorphism, West Bengal population INTRODUCTION The human circulatory system or the cardiovascular system circulates blood and other essential nutrients throughout the body with the help of various blood vessels. Coronary Artiery Disease (CAD) is one of the most common type of disease that is related to this system [1]. According to a WHO report, 7.3 million people die from coronary heart disease every year accounting for approximately 13% of global deaths . The scenario in India is amongst the worst making it the “coronary heart disease capital of the world”. This has led to the growing demand for additional tools to help clinicians identify the “vulnerable” patient at risk for CAD. Access this article online Quick Response Code Website:
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