{"title":"Study of the Association of PCSK9/Eam1104I Gene Polymorphism with Plasma Lipid Concentration and CAD in West Bengal Population","authors":"S. Maiti, Pranamita Biswas, S. Banerjee, N. Jana","doi":"10.21276/IJLSSR.2017.3.5.1","DOIUrl":null,"url":null,"abstract":"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:","PeriodicalId":22509,"journal":{"name":"The International Journal of Life-Sciences Scientific Research","volume":"30 1","pages":"1271-1277"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The International Journal of Life-Sciences Scientific Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21276/IJLSSR.2017.3.5.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
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: