Thrombosis and Haemostasis Research Unit, Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
Thromb Haemost. 2023 Mar;123(3):307-316. doi: 10.1055/s-0042-1760258. Epub 2023 Jan 5.
New biomarkers are warranted to identify patients with coronary artery disease (CAD) at high risk of recurrent cardiovascular events. It has been reported that the expression of microRNAs (miRs) may influence the development of CAD.
We aimed to investigate whether the expression of selected candidate miRs is a predictor of cardiovascular events in a cohort of stable CAD patients.
We performed a single-center prospective study of 749 stable CAD patients with a median follow-up of 2.8 years. We investigated the expression of nine candidate miRs and their relation to cardiovascular events in this cohort. The primary endpoint was the composite of nonfatal myocardial infarction (MI), stent thrombosis (ST), ischemic stroke, and cardiovascular death. The composite of nonfatal MI and ST was analyzed as a secondary endpoint. Furthermore, nonfatal MI, ST, ischemic stroke, and all-cause mortality were analyzed as individual endpoints.
Employing receiver operating characteristic curves, it was shown that compared with traditional cardiovascular risk factors alone, combining the expression of miR-223-3p with existing traditional cardiovascular risk factors increased the predictive value of ST (area under the curve: 0.88 vs. 0.77, = 0.04), the primary composite endpoint (0.65 vs. 0.61, = 0.049), and the secondary endpoint of the composite of nonfatal MI and ST (0.68 vs. 0.62, = 0.04).
Among patients with CAD, adding miR-223-3p expression to traditional cardiovascular risk factors may improve prediction of cardiovascular events, particularly ST. Clinical trials confirming these findings are warranted.
需要新的生物标志物来识别发生复发性心血管事件风险高的冠心病(CAD)患者。已有报道称,microRNAs(miRs)的表达可能影响 CAD 的发生发展。
我们旨在研究选定候选 miRs 的表达是否可预测稳定 CAD 患者队列中的心血管事件。
我们对 749 例稳定 CAD 患者进行了单中心前瞻性研究,中位随访时间为 2.8 年。我们研究了该队列中 9 种候选 miRs 的表达及其与心血管事件的关系。主要终点为非致死性心肌梗死(MI)、支架血栓形成(ST)、缺血性卒中和心血管死亡的复合终点。将非致死性 MI 和 ST 的复合终点作为次要终点进行分析。此外,还将非致死性 MI、ST、缺血性卒中和全因死亡率作为单独的终点进行分析。
采用受试者工作特征曲线显示,与单独使用传统心血管危险因素相比,将 miR-223-3p 的表达与现有的传统心血管危险因素相结合,提高了 ST(曲线下面积:0.88 比 0.77, = 0.04)、主要复合终点(0.65 比 0.61, = 0.049)和非致死性 MI 和 ST 复合终点(0.68 比 0.62, = 0.04)的预测价值。
在 CAD 患者中,将 miR-223-3p 的表达与传统心血管危险因素相结合,可能改善对心血管事件的预测,尤其是 ST。需要进行临床试验来证实这些发现。