Emergency center, The First Affiliated Hospital of Army Medical University, Chongqing, China.
Eur J Clin Invest. 2022 Dec;52(12):e13867. doi: 10.1111/eci.13867. Epub 2022 Sep 8.
A potential inflammatory biomarker, soluble urokinase-type plasminogen activator receptor (suPAR) has been utilized to assist the prognostic assessment of coronary artery disease (CAD) patients; however, outcomes have been inconsistent. The prognostic relevance of suPAR as a predictor of CAD patient adverse outcomes was therefore examined.
Research articles published as of 1 January 2022 were retrieved from PubMed, Embase, the Web of Science and the Cochrane Library. All-cause mortality, cardiovascular mortality and other major cardiovascular events (nonfatal myocardial infarction, heart failure or stroke) were analysed as a subset of relevant studies' results. We calculated hazard ratios (HRs) and 95% confidence intervals (CIs) for each study. The broad EQUATOR guidelines were conformed. Risk of bias was assessed with ROBINS-I tool.
In total, this analysis included nine studies including 14,738 CAD patients. All included studies made a correction for certain potential confounders. However, risk of bias ranged from moderate to critical. When the ROBINS-I tool was used. Patients with CAD that exhibited increased suPAR levels had a substantially higher risk of all-cause mortality (HR = 2.24; 95% CI 1.97-2.55) or cardiovascular mortality (HR = 2.02; 95% CI 1.58-2.58), but not of developing other major cardiovascular events (HR = 1.63; 95% CI 0.86-3.11). Considerable heterogeneity across studies was observed in our meta-analyses, but no significant publication bias was detected.
In patients with coronary disease, suPAR may have prognostic value for both all-cause and cardiovascular mortality but not for other major cardiovascular events.
可溶性尿激酶型纤溶酶原激活物受体(suPAR)作为一种潜在的炎症生物标志物,已被用于辅助冠心病(CAD)患者的预后评估,但结果并不一致。因此,本研究旨在探讨 suPAR 作为 CAD 患者不良预后预测因子的预后相关性。
截至 2022 年 1 月 1 日,从 PubMed、Embase、Web of Science 和 Cochrane 图书馆检索发表的研究文章。将全因死亡率、心血管死亡率和其他主要心血管事件(非致命性心肌梗死、心力衰竭或中风)作为相关研究结果的一个子集进行分析。我们为每个研究计算了风险比(HR)和 95%置信区间(CI)。研究遵循了广泛的 EQUATOR 指南。使用 ROBINS-I 工具评估了偏倚风险。
本分析共纳入 9 项研究,包括 14738 例 CAD 患者。所有纳入的研究都对某些潜在的混杂因素进行了校正。然而,偏倚风险从中度到高度不等。使用 ROBINS-I 工具时,suPAR 水平升高的 CAD 患者全因死亡率(HR=2.24;95%CI 1.97-2.55)或心血管死亡率(HR=2.02;95%CI 1.58-2.58)的风险显著增加,但发生其他主要心血管事件(HR=1.63;95%CI 0.86-3.11)的风险没有增加。荟萃分析中观察到研究之间存在显著的异质性,但未检测到显著的发表偏倚。
在患有冠状动脉疾病的患者中,suPAR 可能对全因和心血管死亡率具有预后价值,但对其他主要心血管事件没有预测价值。