Schulte Christian, Molz Simon, Appelbaum Sebastian, Karakas Mahir, Ojeda Francisco, Lau Denise M, Hartmann Tim, Lackner Karl J, Westermann Dirk, Schnabel Renate B, Blankenberg Stefan, Zeller Tanja
Department of General and Interventional Cardiology, University Heart Center Hamburg Eppendorf, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner site Hamburg/Luebeck/Kiel, Hamburg, Germany.
PLoS One. 2015 Dec 31;10(12):e0145930. doi: 10.1371/journal.pone.0145930. eCollection 2015.
Circulating microRNAs (miRNAs) have been described as potential diagnostic biomarkers in cardiovascular disease and in particular, coronary artery disease (CAD). Few studies were undertaken to perform analyses with regard to risk stratification of future cardiovascular events. miR-126, miR-197 and miR-223 are involved in endovascular inflammation and platelet activation and have been described as biomarkers in the diagnosis of CAD. They were identified in a prospective study in relation to future myocardial infarction.
The aim of our study was to further evaluate the prognostic value of these miRNAs in a large prospective cohort of patients with documented CAD.
Levels of miR-126, miR-197 and miR-223 were evaluated in serum samples of 873 CAD patients with respect to the endpoint cardiovascular death. miRNA quantification was performed using real time polymerase chain reaction (RT-qPCR).
The median follow-up period was 4 years (IQR 2.78-5.04). The median age of all patients was 64 years (IQR 57-69) with 80.2% males. 38.9% of the patients presented with acute coronary syndrome (ACS), 61.1% were diagnosed with stable angina pectoris (SAP). Elevated levels of miRNA-197 and miRNA-223 reliably predicted future cardiovascular death in the overall group (miRNA-197: hazard ratio (HR) 1.77 per one standard deviation (SD) increase (95% confidence interval (CI) 1.20; 2.60), p = 0.004, C-index 0.78; miRNA-223: HR 2.23 per one SD increase (1.20; 4.14), p = 0.011, C-index 0.80). In ACS patients the prognostic power of both miRNAs was even higher (miRNA-197: HR 2.24 per one SD increase (1.25; 4.01), p = 0.006, C-index 0.89); miRA-223: HR 4.94 per one SD increase (1.42; 17.20), p = 0.012, C-index 0.89).
Serum-derived circulating miRNA-197 and miRNA-223 were identified as predictors for cardiovascular death in a large patient cohort with CAD. These results reinforce the assumption that circulating miRNAs are promising biomarkers with prognostic value with respect to future cardiovascular events.
循环微RNA(miRNA)已被描述为心血管疾病尤其是冠状动脉疾病(CAD)的潜在诊断生物标志物。很少有研究针对未来心血管事件的风险分层进行分析。miR-126、miR-197和miR-223参与血管内炎症和血小板活化,并且已被描述为CAD诊断中的生物标志物。它们是在一项关于未来心肌梗死的前瞻性研究中被鉴定出来的。
我们研究的目的是在一大组有记录的CAD患者的前瞻性队列中进一步评估这些miRNA的预后价值。
在873例CAD患者的血清样本中评估miR-126、miR-197和miR-223的水平,以心血管死亡为终点。使用实时聚合酶链反应(RT-qPCR)进行miRNA定量。
中位随访期为4年(四分位间距2.78 - 5.04)。所有患者的中位年龄为64岁(四分位间距57 - 69),男性占80.2%。38.9%的患者表现为急性冠状动脉综合征(ACS),61.1%被诊断为稳定型心绞痛(SAP)。miRNA-197和miRNA-223水平升高可靠地预测了总体组未来的心血管死亡(miRNA-197:每增加一个标准差(SD),风险比(HR)为1.77(95%置信区间(CI)1.20;2.60),p = 0.004,C指数0.78;miRNA-223:每增加一个SD,HR为2.23(1.20;4.14),p = 0.011,C指数0.80)。在ACS患者中,这两种miRNA的预后能力甚至更高(miRNA-197:每增加一个SD,HR为2.24(1.25;4.01),p = 0.006,C指数0.89);miRA-223:每增加一个SD,HR为4.94(1.42;17.20),p = 0.012,C指数0.89)。
血清来源的循环miRNA-197和miRNA-223被鉴定为一大组CAD患者心血管死亡的预测指标。这些结果强化了这样一种假设,即循环miRNA是具有关于未来心血管事件预后价值的有前景的生物标志物。