Circulating microRNA as a Biomarker for Coronary Artery Disease

被引:28
作者
Fazmin, Ibrahim T. [1 ,2 ]
Achercouk, Zakaria [1 ]
Edling, Charlotte E. [1 ]
Said, Asri [3 ]
Jeevaratnam, Kamalan [1 ]
机构
[1] Univ Surrey, Fac Hlth & Med Sci, Guildford GU2 7AL, Surrey, England
[2] Univ Cambridge, Sch Clin Med, Cambridge CB2 1TN, England
[3] Univ Malaysia Sarawak, Sch Med, Sarawak 94300, Malaysia
关键词
coronary artery disease; biomarkers; noncoding RNA; microRNA; RECEPTOR; 4; SIGNAL; MEDIATED TRANSFER; DOWN-REGULATION; MESSENGER-RNAS; PLASMA; EXPRESSION; ATHEROSCLEROSIS; CELLS; GROWTH; AGE;
D O I
10.3390/biom10101354
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Coronary artery disease (CAD) is the leading cause of sudden cardiac death in adults, and new methods of predicting disease and risk-stratifying patients will help guide intervention in order to reduce this burden. Current CAD detection involves multiple modalities, but the consideration of other biomarkers will help improve reliability. The aim of this narrative review is to help researchers and clinicians appreciate the growing relevance of miRNA in CAD and its potential as a biomarker, and also to suggest useful miRNA that may be targets for future study. We sourced information from several databases, namely PubMed, Scopus, and Google Scholar, when collating evidentiary information. MicroRNAs (miRNA) are short, noncoding RNAs that are relevant in cardiovascular physiology and pathophysiology, playing roles in cardiac hypertrophy, maintenance of vascular tone, and responses to vascular injury. CAD is associated with changes in miRNA expression profiles, and so are its risk factors, such as abnormal lipid metabolism and inflammation. Thus, they may potentially be biomarkers of CAD. Nevertheless, there are limitations in using miRNA. These include cost and the presence of several confounding factors that may affect miRNA profiles. Furthermore, there is difficulty in the normalisation of miRNA values between published studies, due to pre-analytical variations in samples.
引用
收藏
页码:1 / 21
页数:21
相关论文
共 144 条
[1]   Plasma MicroRNA 499 as a Biomarker of Acute Myocardial Infarction [J].
Adachi, Taichi ;
Nakanishi, Michio ;
Otsuka, Yoritaka ;
Nishimura, Kunihiro ;
Hirokawa, Gou ;
Goto, Yoichi ;
Nonogi, Hiroshi ;
Iwai, Naoharu .
CLINICAL CHEMISTRY, 2010, 56 (07) :1183-1185
[2]   Circulating microRNA-1 as a potential novel biomarker for acute myocardial infarction [J].
Ai, Jing ;
Zhang, Rong ;
Li, Yue ;
Pu, Jielin ;
Lu, Yanjie ;
Jiao, Jundong ;
Li, Kang ;
Yu, Bo ;
Li, Zhuqin ;
Wang, Rongrong ;
Wang, Lihong ;
Li, Qiang ;
Wang, Nina ;
Shan, Hongli ;
Li, Zhongyu ;
Yang, Baofeng .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (01) :73-77
[3]   Circulating endothelium-enriched microRNA-126 as a potential biomarker for coronary artery disease in type 2 diabetes mellitus patients [J].
Al-Kafaji, Ghada ;
Al-Mahroos, Ghazi ;
Al-Muhtaresh, Haifa Abdulla ;
Sabry, Mohamed Abdalla ;
Razzak, Rima Abdul ;
Salem, Abdel Halim .
BIOMARKERS, 2017, 22 (3-4) :268-278
[4]   Upregulation of Circulating Cardiomyocyte-Enriched miR-1 and miR-133 Associate with the Risk of Coronary Artery Disease in Type 2 Diabetes Patients and Serve as Potential Biomarkers [J].
Al-Muhtaresh, Haifa Abdulla ;
Salem, Abdel Halim ;
Al-Kafaji, Ghada .
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2019, 12 (04) :347-357
[5]  
Albanese M., MICRO RNAS ARE MINOR, DOI [10.1101/2020.05.20.106393v1.abstract, DOI 10.1101/2020.05.20.106393V1.ABSTRACT]
[6]  
[Anonymous], 2018, 2016 DIAGNOSTIC BIOM, P3
[7]   Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma [J].
Arroyo, Jason D. ;
Chevillet, John R. ;
Kroh, Evan M. ;
Ruf, Ingrid K. ;
Pritchard, Colin C. ;
Gibson, Donald F. ;
Mitchell, Patrick S. ;
Bennett, Christopher F. ;
Pogosova-Agadjanyan, Era L. ;
Stirewalt, Derek L. ;
Tait, Jonathan F. ;
Tewari, Muneesh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (12) :5003-5008
[8]  
Auber Martin, 2019, J Extracell Vesicles, V8, P1656042, DOI 10.1080/20013078.2019.1656042
[9]   RNA-Based Therapeutics: From Antisense Oligonucleotides to miRNAs [J].
Bajan, Sarah ;
Hutvagner, Gyorgy .
CELLS, 2020, 9 (01)
[10]   Cardiac fibroblast-derived microRNA passenger strand-enriched exosomes mediate cardiomyocyte hypertrophy [J].
Bang, Claudia ;
Batkai, Sandor ;
Dangwal, Seema ;
Gupta, Shashi Kumar ;
Foinquinos, Ariana ;
Holzmann, Angelika ;
Just, Annette ;
Remke, Janet ;
Zimmer, Karina ;
Zeug, Andre ;
Ponimaskin, Evgeni ;
Schmiedl, Andreas ;
Yin, Xiaoke ;
Mayr, Manuel ;
Halder, Rashi ;
Fischer, Andre ;
Engelhardt, Stefan ;
Wei, Yuanyuan ;
Schober, Andreas ;
Fiedler, Jan ;
Thum, Thomas .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (05) :2136-2146