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Elevated Plasma Levels of Circulating Extracellular miR-320a-3p in Patients with Paroxysmal Atrial Fibrillation

机译:阵发性心房颤动患者血浆中循环细胞外miR-320a-3p水平升高

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摘要

The potential of extracellular circulating microRNAs (miRNAs) as non-invasive biomarkers of atrial fibrillation (AF) has been confirmed by a number of recent studies. However, the current data for some miRNAs are controversial and inconsistent, probably due to pre-analytical and methodological differences. In this work, we attempted to fulfill the basic pre-analytical requirements provided for circulating miRNA studies for application to paroxysmal atrial fibrillation (PAF) research. We used quantitative PCR (qPCR) to determine the relative plasma levels of circulating miRNAs expressed in the heart or associated with atrial remodeling or fibrillation with reported altered plasma/serum levels in AF: miR-146a-5p, miR-150-5p, miR-19a-3p, miR-21-5p, miR-29b-3p, miR-320a-3p, miR-328-3p, miR-375-3p, and miR-409-3p. First, in a cohort of 90 adult outpatient clinic patients, we found that the plasma level of miR-320a-3p was elevated in PAF patients compared to healthy controls and hypertensive patients without AF. We further analyzed the impact of medication therapies on miRNA relative levels and found elevated miR-320a-3p levels in patients receiving angiotensin-converting-enzyme inhibitors (ACEI) therapy. Additionally, we found that miR-320a-3p, miR-21-5p, and miR-146a-5p plasma levels positively correlated with the CHA DS -Vasc score and were elevated in subjects with CHA DS -Vasc ≥ 2. Our results indicate that, amongst the analyzed miRNAs, miR-320a-3p may be considered as a potential PAF circulating plasma biomarker, leading to speculation as to whether this miRNA is a marker of platelet state change due to ACEI therapy.
机译:大量近期研究证实了细胞外循环微RNA(miRNA)作为房颤(AF)非侵入性生物标志物的潜力。但是,某些miRNA的当前数据存在争议且不一致,可能是由于分析前和方法学上的差异。在这项工作中,我们试图满足为循环miRNA研究提供的基本分析前要求,以用于阵发性心房颤动(PAF)研究。我们使用定量PCR(qPCR)来确定在心脏中表达的或与房颤重塑或原纤维形成有关的循环miRNA的相对血浆水平,其中房颤/血浆水平据报道有所改变:miR-146a-5p,miR-150-5p,miR -19a-3p,miR-21-5p,miR-29b-3p,miR-320a-3p,miR-328-3p,miR-375-3p和miR-409-3p。首先,在队列的90名成人门诊患者中,我们发现PAF患者的miR-320a-3p血浆水平高于健康对照组和无AF的高血压患者。我们进一步分析了药物治疗对miRNA相对水平的影响,发现接受血管紧张素转换酶抑制剂(ACEI)治疗的患者中miR-320a-3p水平升高。此外,我们发现miR-320a-3p,miR-21-5p和miR-146a-5p血浆水平与CHA DS -Vasc得分呈正相关,并且在CHA DS -Vasc≥2的受试者中升高。在分析的miRNA中,miR-320a-3p可能被认为是潜在的PAF循环血浆生物标志物,导致人们猜测该miRNA是否是由于ACEI治疗引起的血小板状态改变的标志物。

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