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Change in lipoprotein-associated phospholipase A2 and its association with cardiovascular outcomes in patients with acute coronary syndrome

机译:急性冠状动脉综合征患者脂蛋白相关磷脂酶A2的变化及其与心血管预后的关系

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摘要

Lipoprotein-associated phospholipase A2 (Lp-PLA2) probably plays an important role in the development of acute coronary syndrome (ACS). However, alterations of Lp-PLA2 levels during ACS and its association with cardiovascular outcome are unclear. Our aim was to investigate the change in Lp-PLA2 and its association with cardiovascular outcome in patients with ACS.A total of 79 patients with ACS came from the coronary care unit (CCU) between June 1, 2015 and August 31, 2016 in this longitudinal study. Serum levels of Lp-PLA2, troponin I, and creatine kinase isoenzymes MB (CK-MB) were measured at admission, on the first morning (D1), on the second morning of hospitalization (D2), and on the last second morning before discharge (D4). The patients were followed up till November 30, 2016. The primary outcomes were cardiovascular death and cardiovascular rehospitalization. Kaplan–Meier analysis and Cox proportional hazard models were used to identify risk factors for poor outcome in patients with ACS.All patients were followed up for 10.6 ± 4.7 months. The patients were divided into 2 groups according to the median of Lp-PLA2: lower Lp-PLA2 group and higher Lp-PLA2 group. Elevated levels of Lp-PLA2 significantly decreased during the early phases of ACS in higher Lp-PLA2 group. And Lp-PLA2 level increased at first and then decreased in lower Lp-PLA2 group. Kaplan–Meier analysis showed that patients with elevated Lp-PLA2 had a lower cardiovascular event-free survival (log-rank χ2 = 4.736, P = .030) than those with lower Lp-PLA2. Cox regression analysis indicated that high Lp-PLA2 level (hazard ratio [HR] = 1.005, 95% confidence interval [CI] = 1.002–1.008, P = .003), time delay from symptom onset to admission (HR = 1.088, 95% CI = 1.038–1.139, P < .001) independently predicted cardiovascular event in patients with ACS after adjusting for potential confounders.Serum level of Lp-PLA2 altered considerably during the early phase of ACS and increased Lp-PLA2 independently predicted cardiovascular outcome in patients with ACS after adjustment for potential confounders.
机译:脂蛋白相关的磷脂酶A2(Lp-PLA2)可能在急性冠状动脉综合征(ACS)的发展中起重要作用。但是,尚不清楚ACS期间Lp-PLA2水平的变化及其与心血管预后的关系。我们的目的是调查ACS患者Lp-PLA2的变化及其与心血管结局的关系.2015年6月1日至2016年8月31日之间,共有79例ACS患者来自冠心病监护病房(CCU)。纵向研究。在入院时,住院第一天(D1),住院第二天(D2)和之前的最后第二天早晨测量血清Lp-PLA2,肌钙蛋白I和肌酸激酶同工酶MB(CK-MB)放电(D4)。对患者进行了随访,直到2016年11月30日。主要结果是心血管死亡和心血管再入院。采用Kaplan–Meier分析和Cox比例风险模型确定ACS患者预后不良的危险因素。所有患者均获得了10.6±±4.7个月的随访。根据Lp-PLA2的中位数将患者分为2组:较低的Lp-PLA2组和较高的Lp-PLA2组。在较高的Lp-PLA2组中,ACS早期阶段Lp-PLA2的升高水平明显降低。在较低的Lp-PLA2组中,Lp-PLA2水平先升高后降低。 Kaplan–Meier分析显示,Lp-PLA2升高的患者比Lp-PLA2降低的患者无心血管事件生存率低(log-rankχ 2 = 4.736,P = .030)。 Cox回归分析表明,Lp-PLA2水平较高(危险比[HR] = 1.005,95%置信区间[CI] = 1.002-1.008,P = .003),从症状发作到入院的时间延迟(HR = 1.088,95)校正潜在混杂因素后,%CI = 1.038–1.139,P <.001)独立预测ACS患者的心血管事件。ACS早期,Lp-PLA2的血清水平发生了显着变化,而Lp-PLA2的升高独立预测了心血管疾病的发生。调整了潜在混杂因素后的ACS患者。

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