Association of ET1 and APE1 Genes Polymorphism with Coronary Artery Disease

S. T. Raza, A. Eba, Irshad A. Wani, Sanchita Srivastava, F. Mahdi
{"title":"Association of ET1 and APE1 Genes Polymorphism with Coronary Artery Disease","authors":"S. T. Raza, A. Eba, Irshad A. Wani, Sanchita Srivastava, F. Mahdi","doi":"10.1055/s-0044-1788069","DOIUrl":null,"url":null,"abstract":"Abstract Coronary artery disease (CAD) is one of the most common cardiovascular diseases (CVDs), being the foremost reason for mortality and disability globally. It is a cascade of polygenic architecture of various disorders as a resultant of complexities between various genetic factors and environmental factors. The aim of the present study was to investigate whether the ET1 and APE1 gene polymorphism is associated with the susceptibility to CAD. This study was approved by the Ethical Review Committee of Era Medical College and Hospital. Three milliliters of venous blood sample was collected in ethylenediaminetetraacetic acid-coated vials, and genomic DNA was isolated by using the standard phenol-chloroform extraction method for restriction fragment length polymorphism-polymerase chain reaction study. The APE1 gene AA, AG, GG, and AG + GG genotypes frequencies were 13.91, 40.87, 45.22, and 86.99% in CAD cases and 13, 50, 37, and 87% in controls, respectively. The ET1 gene GG, GT, TT, GT + TT genotypes frequencies were 6.67, 37.5, 55.8, and 93.34% in CAD cases and 6.67, 25.33, 68, and 93.34% in controls. The ET1 and APE1 gene polymorphisms were not significantly associated with the risk of CAD.","PeriodicalId":506654,"journal":{"name":"International Journal of Angiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Angiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-0044-1788069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Coronary artery disease (CAD) is one of the most common cardiovascular diseases (CVDs), being the foremost reason for mortality and disability globally. It is a cascade of polygenic architecture of various disorders as a resultant of complexities between various genetic factors and environmental factors. The aim of the present study was to investigate whether the ET1 and APE1 gene polymorphism is associated with the susceptibility to CAD. This study was approved by the Ethical Review Committee of Era Medical College and Hospital. Three milliliters of venous blood sample was collected in ethylenediaminetetraacetic acid-coated vials, and genomic DNA was isolated by using the standard phenol-chloroform extraction method for restriction fragment length polymorphism-polymerase chain reaction study. The APE1 gene AA, AG, GG, and AG + GG genotypes frequencies were 13.91, 40.87, 45.22, and 86.99% in CAD cases and 13, 50, 37, and 87% in controls, respectively. The ET1 gene GG, GT, TT, GT + TT genotypes frequencies were 6.67, 37.5, 55.8, and 93.34% in CAD cases and 6.67, 25.33, 68, and 93.34% in controls. The ET1 and APE1 gene polymorphisms were not significantly associated with the risk of CAD.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ET1 和 APE1 基因多态性与冠状动脉疾病的关系
摘要 冠状动脉疾病(CAD)是最常见的心血管疾病(CVDs)之一,是导致全球死亡和残疾的首要原因。由于各种遗传因素和环境因素之间的复杂性,冠状动脉疾病是一种多基因结构的连锁反应。本研究旨在探讨 ET1 和 APE1 基因多态性是否与 CAD 易感性相关。本研究已获得年代医学院和医院伦理审查委员会的批准。在涂有乙二胺四乙酸的小瓶中采集三毫升静脉血样本,采用标准苯酚-氯仿提取法分离基因组DNA,进行限制性片段长度多态性-聚合酶链反应研究。在 CAD 病例中,APE1 基因 AA、AG、GG 和 AG + GG 的基因型频率分别为 13.91%、40.87%、45.22% 和 86.99%;在对照组中,APE1 基因 AA、AG、GG 和 AG + GG 的基因型频率分别为 13%、50%、37% 和 87%。在 CAD 病例中,ET1 基因的 GG、GT、TT、GT + TT 基因型频率分别为 6.67%、37.5%、55.8% 和 93.34%;在对照组中,ET1 基因的 GG、GT、TT、GT + TT 基因型频率分别为 6.67%、25.33%、68% 和 93.34%。ET1 和 APE1 基因多态性与 CAD 风险无显著相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Major Delay in Door-to-Ballon Time for Primary Percutaneous Coronary Intervention is Not Related to Interventional Cardiologist's Late Arrival Atherogenic Effect of Homocysteine, a Biomarker of Inflammation and Its Treatment Venous Thromboembolism: Current Insights and Future Directions Association of ET1 and APE1 Genes Polymorphism with Coronary Artery Disease Comparative Efficacy of Hypertension Management Strategies
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1