• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

微小RNA-224(rs188519172 A>G)基因变异与冠状动脉疾病易感性降低相关:一项病例对照研究。

MicroRNA-224 (rs188519172 A>G) Gene Variability is Associated with a Decreased Susceptibility to Coronary Artery Disease: A Case-Control Study.

作者信息

Mir Rashid, Jha Chandan K, Elfaki Imadeldin, Rehman Suriya, Javid Jamsheed, Khullar Naina, Banu Shaheena, Chahal Sukh Mohinder Singh

机构信息

Department of Medical Lab Technology, Faculty of Applied Medical Sciences, University of Tabuk, Tabuk, Saudi Arabia.

Department of Human Genetics, Punjabi University, Patiala, Punjab, India.

出版信息

Microrna. 2019;8(3):198-205. doi: 10.2174/2211536608666181211153859.

DOI:10.2174/2211536608666181211153859
PMID:30539710
Abstract

AIM

The microRNAs regulate the expression of multiple genes involved in diseases such as cancer, diabetes and cardiovascular disease. In this study, we have investigated the association between the miR-224 gene polymorphism (rs188519172A>G) and susceptibility of coronary artery disease CAD.

METHODOLOGY

Hundred CAD patients and 100-matched healthy control were included. Genotyping of the miR-224 (rs188519172A>G) polymorphism was performed using Amplification refractory mutation system PCR method (ARMS-PCR).

RESULTS

A significant difference was observed in the genotype distribution among CAD patients and healthy controls (P=0.018). The frequencies of all three genotypes GG, GA, AA reported in the patient's samples were 33%, 66% and 01%, and in the healthy controls samples, were 16%, 82% and 2% respectively. A multivariate analysis based on logistic regression was conducted for each group to estimate the association between miR-224 rs188519172 genotypes and risk to coronary artery disease. Results show that the miR-224 (rs188519172 A>G) polymorphism was associated with a decreased risk to CAD in a codominant model, GA genotype vs. GG (OR = 0.39 (95 % CI, 0.19-0.76), RR 0.58 (0.38-0.90, P=0.006). In the dominant model, (GA+AA vs. GG), there was also a significant association with the OR=0.38 (95 % CI (0.19-0.76), RR 0.58 (0.38-0.89), and P=0.006. Whereas, in the recessive model, (GG+GA vs. AA), there was no significant association of CAD with OR=0.49 (95% CI (0.044-5.54), RR 0.74 (0.33-1.68), and P=0.48.

CONCLUSION

Our findings indicated that miR-224 (rs188519172) GA genotype is associated with a decreased susceptibility to CAD.

摘要

目的

微小RNA调控多种与癌症、糖尿病和心血管疾病等疾病相关的基因表达。在本研究中,我们调查了miR - 224基因多态性(rs188519172A>G)与冠状动脉疾病(CAD)易感性之间的关联。

方法

纳入100例CAD患者和100例匹配的健康对照。采用扩增阻滞突变系统PCR方法(ARMS - PCR)对miR - 224(rs188519172A>G)多态性进行基因分型。

结果

CAD患者和健康对照的基因型分布存在显著差异(P = 0.018)。患者样本中报告的所有三种基因型GG、GA、AA的频率分别为33%、66%和1%,而在健康对照样本中分别为16%、82%和2%。对每组进行基于逻辑回归的多变量分析,以估计miR - 224 rs188519172基因型与冠状动脉疾病风险之间的关联。结果显示,在共显性模型中,miR - 224(rs188519172 A>G)多态性与CAD风险降低相关,GA基因型与GG基因型相比(比值比=0.39(95%置信区间,0.19 - 0.76),相对风险0.58(0.38 - 0.90),P = 0.006)。在显性模型中,(GA + AA与GG相比),也存在显著关联,比值比=0.38(95%置信区间(0.19 - 0.76),相对风险0.58(0.38 - 0.89),P = 0.006)。然而,在隐性模型中,(GG + GA与AA相比),CAD与比值比=0.49(95%置信区间(0.044 - 5.54),相对风险0.74(0.33 - 1.68),P = 0.48)无显著关联。

结论

我们的研究结果表明,miR - 224(rs188519172)GA基因型与CAD易感性降低相关。

相似文献

1
MicroRNA-224 (rs188519172 A>G) Gene Variability is Associated with a Decreased Susceptibility to Coronary Artery Disease: A Case-Control Study.微小RNA-224(rs188519172 A>G)基因变异与冠状动脉疾病易感性降低相关:一项病例对照研究。
Microrna. 2019;8(3):198-205. doi: 10.2174/2211536608666181211153859.
2
Potential Impact of MicroRNA-423 Gene Variability in Coronary Artery Disease.微小RNA-423基因变异性在冠状动脉疾病中的潜在影响
Endocr Metab Immune Disord Drug Targets. 2019;19(1):67-74. doi: 10.2174/1871530318666181005095724.
3
Molecular Evaluation of MicroRNA-146 Gene Variability (rs2910164 C> G) and its Association with Increased Susceptibility to Coronary Artery Disease.miR-146 基因变异(rs2910164 C>G)的分子评估及其与冠心病易感性增加的关联。
Microrna. 2020;9(5):363-372. doi: 10.2174/2211536609666201209151130.
4
Incidence of MicroR-4513C/T Gene Variability in Coronary Artery Disease - A Case-Control Study.冠心病中微小RNA-4513 C/T基因变异性的发生率——一项病例对照研究
Endocr Metab Immune Disord Drug Targets. 2019;19(8):1216-1223. doi: 10.2174/1871530319666190417111940.
5
Potential Impact of Gene Polymorphism in Coronary Artery Disease.基因多态性在冠状动脉疾病中的潜在影响。
J Cardiovasc Dev Dis. 2018 Jul 13;5(3):38. doi: 10.3390/jcdd5030038.
6
The rs2070895 (-250G/A) Single Nucleotide Polymorphism in Hepatic Lipase (HL) Gene and the Risk of Coronary Artery Disease in North Indian Population: A Case-Control Study.肝脂酶(HL)基因中的rs2070895(-250G/A)单核苷酸多态性与北印度人群冠状动脉疾病风险:一项病例对照研究。
J Clin Diagn Res. 2016 Aug;10(8):GC01-6. doi: 10.7860/JCDR/2016/20496.8378. Epub 2016 Aug 1.
7
Myeloperoxidase G-463A polymorphism and susceptibility to coronary artery disease: a meta-analysis.髓过氧化物酶 G-463A 多态性与冠心病易感性的关系:一项荟萃分析。
Gene. 2013 Jul 10;523(2):152-7. doi: 10.1016/j.gene.2013.03.131. Epub 2013 Apr 10.
8
Biological and Clinical Implications of TNF-α Promoter and CYP1B1 Gene Variations in Coronary Artery Disease Susceptibility.TNF-α 启动子和 CYP1B1 基因变异与冠心病易感性的生物学和临床意义。
Cardiovasc Hematol Disord Drug Targets. 2021;21(4):266-277. doi: 10.2174/1871529X22666211221151830.
9
Clinical Utility of Amplification Refractory Mutation System-Based PCR and Mutation-Specific PCR for Precise and Rapid Genotyping of Angiotensin-Converting Enzyme 1 (ACE1-rs4646996 D>I) and Angiotensin-Converting Enzyme 2 (ACE2-rs4240157T>C) Gene Variations in Coronary Artery Disease and Their Strong Association with Its Disease Susceptibility and Progression.基于扩增阻滞突变系统的聚合酶链反应和突变特异性聚合酶链反应在冠状动脉疾病中对血管紧张素转换酶1(ACE1-rs4646996 D>I)和血管紧张素转换酶2(ACE2-rs4240157T>C)基因变异进行精确快速基因分型的临床应用及其与疾病易感性和进展的强关联。
Diagnostics (Basel). 2022 May 26;12(6):1321. doi: 10.3390/diagnostics12061321.
10
A functional polymorphism in the promoter of miR-17-92 cluster is associated with decreased risk of ischemic stroke.miR-17-92 簇启动子中的功能性多态性与缺血性脑卒中风险降低相关。
BMC Med Genomics. 2019 Nov 8;12(1):159. doi: 10.1186/s12920-019-0589-1.

引用本文的文献

1
Molecular Determination of Vascular Endothelial Growth Factor, miRNA-423 Gene Abnormalities by Utilizing ARMS-PCR and Their Association with Fetal Hemoglobin Expression in the Patients with Sickle Cell Disease.利用扩增阻滞突变系统聚合酶链反应(ARMS-PCR)对镰状细胞病患者血管内皮生长因子、miRNA-423基因异常进行分子检测及其与胎儿血红蛋白表达的关联研究
Curr Issues Mol Biol. 2022 Jun 1;44(6):2569-2582. doi: 10.3390/cimb44060175.
2
Role of MicroRNAs in the Pathogenesis of Coronary Artery Disease.微小RNA在冠状动脉疾病发病机制中的作用
Front Cardiovasc Med. 2021 Apr 12;8:632392. doi: 10.3389/fcvm.2021.632392. eCollection 2021.
3
Role of Selected miRNAs as Diagnostic and Prognostic Biomarkers in Cardiovascular Diseases, Including Coronary Artery Disease, Myocardial Infarction and Atherosclerosis.
特定微小RNA作为心血管疾病(包括冠状动脉疾病、心肌梗死和动脉粥样硬化)诊断和预后生物标志物的作用
J Cardiovasc Dev Dis. 2021 Feb 19;8(2):22. doi: 10.3390/jcdd8020022.
4
Potential Impact of MicroRNA Gene Polymorphisms in the Pathogenesis of Diabetes and Atherosclerotic Cardiovascular Disease.微小RNA基因多态性在糖尿病和动脉粥样硬化性心血管疾病发病机制中的潜在影响
J Pers Med. 2019 Nov 25;9(4):51. doi: 10.3390/jpm9040051.
5
LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population.低密度脂蛋白受体基因多态性(rs5925和rs1529729)与南印度人群冠状动脉疾病易感性相关。
Med Sci (Basel). 2019 Jul 15;7(7):80. doi: 10.3390/medsci7070080.
6
Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study.印度人群中网膜素1 rs2274907 A>T和rs2274908 G>A基因多态性与冠状动脉疾病相关性的评估:一项病例对照研究
J Pers Med. 2019 Jun 6;9(2):30. doi: 10.3390/jpm9020030.