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Lipoprotein Associated- Phospholipase A2 in STEMI Vs. NSTE-ACS Patients: a Marker of Cardiovascular Atherosclerotic Risk Rather Than Thrombosis

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Date 2023 Apr 6
PMID 37022507
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Abstract

Methods: A consecutive cohort of patients undergoing coronary angiography for acute coronary syndrome (ACS) were included and divided according to presentation for non ST-segment elevation-ACS or ST-segment elevation Myocardial Infarction (STEMI). Lp-PLA2 activity was assessed in blood samples drawn at admission using the Diazyme Lp-PlA2 Activity Assay.

Results: We included in our study 117 patients, of whom 31 (26.5%) presented with STEMI. STEMI patients were significantly younger (p = 0.05), displayed a lower rate of hypertension (p = 0.002), previous MI (p = 0.001) and PCI (p = 0.01) and used less frequently statins (p = 0.01) and clopidogrel (p = 0.02). White blood cells and admission glycemia were increased in STEMI (p = 0.001, respectively). The prevalence and severity of CAD was not different according to ACS types, but for a higher prevalence of thrombus (p < 0.001) and lower TIMI flow (p = 0.002) in STEMI. The levels of Lp-PlA2 were significantly lower in STEMI as compared to NSTE-ACS patients, (132 ± 41.1 vs. 154.6 ± 40.9 nmol/min/mL, p = 0.01). In fact, the rate of patients with Lp-PlA2 above the median (148 nmol/min/mL) was significantly lower in STEMI patients as compared to NSTE-ACS (32.3% vs. 57%, p = 0.02, adjusted OR[95% CI] = 0.20[0.06-0.68], p = 0.010). Moreover, a direct linear relationship was observed between Lp-PlA2 and LDL-C (r = 0.47, p < 0.001), but not with inflammatory biomarkers.

Conclusion: The present study shows that among ACS patients, the levels of Lp-PlA2 are inversely associated with STEMI presentation and thrombotic coronary occlusion, being instead increased in NSTE-ACS patients, therefore potentially representing a marker of more aggressive chronic cardiovascular disease with an increased risk of recurrent cardiovascular events.

Citing Articles

Research progress of cPLA2 in cardiovascular diseases (Review).

Lin W, Wang S, Liu R, Zhang D, Zhang J, Qi X Mol Med Rep. 2025; 31(4).

PMID: 39981923 PMC: 11868774. DOI: 10.3892/mmr.2025.13468.

References
1.
Nardin M, Verdoia M, Barbieri L, Schaffer A, Suryapranata H, De Luca G . Radial vs Femoral Approach in Acute Coronary Syndromes: A Meta- Analysis of Randomized Trials. Curr Vasc Pharmacol. 2017; 16(1):79-92. DOI: 10.2174/1570161115666170504125831. View

2.
Wang T . Assessing the role of circulating, genetic, and imaging biomarkers in cardiovascular risk prediction. Circulation. 2011; 123(5):551-65. PMC: 3059807. DOI: 10.1161/CIRCULATIONAHA.109.912568. View

3.
Zethelius B, Berglund L, Sundstrom J, Ingelsson E, Basu S, Larsson A . Use of multiple biomarkers to improve the prediction of death from cardiovascular causes. N Engl J Med. 2008; 358(20):2107-16. DOI: 10.1056/NEJMoa0707064. View

4.
Epps K, Wilensky R . Lp-PLA₂- a novel risk factor for high-risk coronary and carotid artery disease. J Intern Med. 2010; 269(1):94-106. DOI: 10.1111/j.1365-2796.2010.02297.x. View

5.
Liu Y, Hu X, Li H, Jiang W, Wang X, Lin H . Association of lipoprotein-associated phospholipase A₂ with characteristics of vulnerable coronary atherosclerotic plaques. Yonsei Med J. 2011; 52(6):914-22. PMC: 3220251. DOI: 10.3349/ymj.2011.52.6.914. View