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SUN Z Y, LIU X H. Predictive value of lipoprotein(a) for major adverse cardiovascular events in patients with acute coronary syndrome[J]. Chin J Clin Med, xxxx, xx(x): 1-7. DOI: 10.12025/j.issn.1008-6358.2025.20250033
Citation: SUN Z Y, LIU X H. Predictive value of lipoprotein(a) for major adverse cardiovascular events in patients with acute coronary syndrome[J]. Chin J Clin Med, xxxx, xx(x): 1-7. DOI: 10.12025/j.issn.1008-6358.2025.20250033

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

  • 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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