Ward Jeanine A, Esa Nada, Pidikiti Rahul, Freedman Jane E, Keaney John F, Tanriverdi Kahraman, Vitseva Olga, Ambros Victor, Lee Rosalind, McManus David D
Department of Emergency Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Cardiac Electrophysiology Section, Cardiovascular Medicine Division, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Fam Med Med Sci Res. 2013 Oct 1;2(2):108. doi: 10.4172/2327-4972.1000108.
BACKGROUND: Differences in plasma and whole blood expression microRNAs (miRNAs) in patients with an acute coronary syndrome (ACS) have been determined in both in vitro and in vivo studies. Although most circulating miRNAs are located in the cellular components of whole blood, little is known about the miRNA profiles of whole blood subcomponents, including plasma, platelets and leukocytes in patients with myocardial ischemia. METHODS: Thirteen patients with a ST-segment-elevation (STEMI) or non-ST-segment elevation (NSTEMI) myocardial infarction were identified in the University of Massachusetts Medical Center Emergency Department (ED) or cardiac catheterization laboratory between February and June of 2012. Whole blood was obtained from arterial blood samples at the time of cardiac catheterization and cell-specific miRNA profiling was performed. Expression of 343 miRNAs was quantified from whole blood, plasma, platelets, and peripheral blood mononuclear cells using a high-throughput, quantitative Real-Time polymerase-chain reaction system (qRT-PCR). RESULTS: MiRNAs associated with STEMI as compared to NSTEMI patients included miR-25-3p, miR-221-3p, and miR-374b-5p. MiRNA 30d-5p was associated with plasma, platelets, and leukocytes in both STEMI and NSTEMI patients; miRNAs 221-3p and 483-5p were correlated with plasma and platelets only in NSTEMI patients. CONCLUSIONS: Cell-specific miRNA profiles differed between patients with STEMI and NSTEMI. The miRNA distribution is also unique amongst plasma, platelets, and leukocytes in patients with ischemic heart disease or ACS. Our findings suggest unique miRNA profiles among the circulating subcomponents in patients presenting with myocardial ischemia.
背景:急性冠状动脉综合征(ACS)患者血浆和全血中微小RNA(miRNA)表达的差异已在体外和体内研究中得到确定。尽管大多数循环miRNA位于全血的细胞成分中,但对于心肌缺血患者全血亚成分(包括血浆、血小板和白细胞)的miRNA谱了解甚少。 方法:2012年2月至6月期间,在马萨诸塞大学医学中心急诊科(ED)或心导管实验室确定了13例ST段抬高型(STEMI)或非ST段抬高型(NSTEMI)心肌梗死患者。在心脏导管插入术时从动脉血样本中获取全血,并进行细胞特异性miRNA分析。使用高通量定量实时聚合酶链反应系统(qRT-PCR)从全血、血浆、血小板和外周血单核细胞中定量343种miRNA的表达。 结果:与NSTEMI患者相比,与STEMI相关的miRNA包括miR-25-3p、miR-221-3p和miR-374b-5p。miRNA 30d-5p在STEMI和NSTEMI患者的血浆、血小板和白细胞中均有相关性;miRNA 221-3p和483-5p仅在NSTEMI患者的血浆和血小板中相关。 结论:STEMI和NSTEMI患者的细胞特异性miRNA谱不同。在缺血性心脏病或ACS患者的血浆、血小板和白细胞中,miRNA分布也具有独特性。我们的研究结果表明,心肌缺血患者循环亚成分中存在独特的miRNA谱。
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