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用于冠状动脉疾病的微小RNA生物标志物?

MicroRNA Biomarkers for Coronary Artery Disease?

作者信息

Kaudewitz Dorothee, Zampetaki Anna, Mayr Manuel

机构信息

King's British Heart Foundation Centre, King's College London, 125 Coldharbour Lane, London, SE59NU, UK.

出版信息

Curr Atheroscler Rep. 2015 Dec;17(12):70. doi: 10.1007/s11883-015-0548-z.

Abstract

MicroRNA (miRNA, miR) measurements in patients with coronary heart disease are hampered by the confounding effects of medication commonly used in cardiovascular patients such as statins, antiplatelet drugs, and heparin administration. Statins reduce the circulating levels of liver-derived miR-122. Antiplatelet medication attenuates the release of platelet-derived miRNAs. Heparin inhibits the polymerase chain reactions, in particular the amplification of the exogenous Caenorhabditis elegans spike-in control, thereby resulting in an artefactual rise of endogenous miRNAs. As these limitations have not been previously recognised, a reevaluation of the current miRNA literature, in particular of case-control studies in patients with cardiovascular disease or coronary interventions, is required.

摘要

冠心病患者体内微小RNA(miRNA,miR)的检测受到心血管疾病患者常用药物(如他汀类药物、抗血小板药物和肝素)的混杂影响。他汀类药物会降低肝脏来源的miR-122的循环水平。抗血小板药物会减弱血小板来源的miRNA的释放。肝素会抑制聚合酶链反应,尤其是对外源秀丽隐杆线虫加标对照的扩增,从而导致内源性miRNA出现人为升高。由于这些局限性此前未被认识到,因此需要对当前的miRNA文献进行重新评估,尤其是对心血管疾病患者或接受冠状动脉介入治疗患者的病例对照研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a097/4613887/b5c0546d1bd0/11883_2015_548_Fig1_HTML.jpg

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