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脂蛋白a对急性冠脉综合征患者主要心血管不良事件的预测价值

Predictive value of lipoprotein(a) for major adverse cardiovascular events in patients with acute coronary syndrome

  • 摘要:
    目的  探讨脂蛋白alipoprotein(a),Lp(a)水平对急性冠脉综合征(acute coronary syndrome,ACS)患者主要心血管不良事件(major adverse cardiovascular events,MACE)的预测价值。
    方法  回顾性纳入2021年8月至2023年10月于大连市友谊医院住院并完成冠状动脉造影的ACS患者310例,根据Lp(a)水平分为高Lp(a)组(>300 mg/L,n=224)和低Lp(a)组(≤300 mg/L,n=86)。所有患者出院后随访收集MACE发生情况,绘制生存曲线。采用多因素Cox回归分析ACS患者发生MACE的影响因素。
    结果  高Lp(a)组年龄、C反应蛋白、总胆固醇、载脂蛋白B、多支病变比例、冠脉介入治疗(PCI)比例、Gensini评分高于低Lp(a)组,尿酸、左室射血分数(LVEF)低于低Lp(a)组(均P<0.05)。所有ACS患者的中位随访时间为22(17,24)个月,共61例(19.68%)患者发生MACE,高Lp(a)组较低Lp(a)组心绞痛再入院比例和累积MACE发生率更高(P=0.009、P=0.001)。单因素分析结果显示,高Lp(a)水平、糖尿病、心肌梗死、左主干病变、多支病变、PCI、年龄、Gensini评分、LVEF、同型半胱氨酸均与MACE发生显著相关(均P<0.05)。经多因素校正后,高Lp(a)组MACE风险是低Lp(a)组的3.42倍(HR=3.42,P=0.016)。
    结论 Lp(a)>300 mg/L是ACS患者发生MACE的独立危险因素,可作为ACS患者发生MACE的预测指标。

     

    Abstract:
    Objective  To explore the predictive value of lipoprotein(a) (Lpa) levels for major adverse cardiovascular events(MACE) in patients with acute coronary syndrome(ACS).
    Methods  A total of 310 ACS patients who were hospitalized in Dalian Friendship Hospital and completed coronary angiography from August 2021 to October 2023 were included in this study. According to the level of Lp(a), the patients were divided into high Lp(a) group (>300 mg/L, n=224) and low Lp(a) group (≤300 mg/L, n=86). All patients undergo outpatient follow-up after discharge, the occurrence of major MACE was recorded, and multivariate Cox regression analysis was performed to analyze the influencing factors of MACE in ACS patients.
    Results  The age, C-reactive protein, total cholesterol, ApoB, proportion of multiple lesions and PCI, Gensini score of the high Lp(a) group were higher than those of the low Lp(a) group, while uric acid and LVEF were lower than those of the low Lp(a) group (all P<0.05). The median follow-up time for all ACS patients was 22 (17, 24) months, with a total of 61 patients (19.68%) experiencing MACE. The high Lp(a) group had a higher readmission rate and cumulative MACE incidence for angina compared to the low Lp(a) group (P=0.009, P=0.001). Single factor analysis showed that high Lp(a) level, diabetes, myocardial infarction, left main artery disease, multi vessel disease, PCI, age, Gensini score, LVEF, homocysteine are significantly correlated with MACE (all P<0.05). After adjusting for multiple factors, the MACE risk in the high Lp(a) group was 3.42 times higher than that in the low Lp(a) group (HR=3.42, P=0.016).
    Conclusion Lp(a)>300 mg/L is an independent risk factor for the development of MACE in patients with ACS, and can be used as a predictor for the development of MACE in patients with ACS.

     

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