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Prognostic implications of calculated Apo-lipoprotein B in patients with ST-segment elevation myocardial infarction
Saeed Ghodsi1, Mehrnaz Mohebi1, Seyed-Ali Sadre-Bafghi1
1Research department, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Apolipoprotein B (Apo-B) effectively predicts cardiovascular events in ST-segment elevation myocardial infarction (STEMI) patients undergoing primary PCI. This simple calculated Apo-B metric surpasses LDL-C and Non-HDLC in prognostic utility for STEMI patients.
Area of Science:
- Cardiology
- Lipidology
- Cardiovascular Risk Assessment
Background:
- Debates persist regarding the role of lipoproteins, including Apolipoprotein B (Apo-B), in managing coronary artery disease (CAD).
- Apo-B may offer incremental prognostic value in acute ST-segment elevation myocardial infarction (STEMI).
Purpose of the Study:
- To evaluate the prognostic utility of calculated Apo-B in STEMI patients treated with primary percutaneous coronary intervention (PCI).
Main Methods:
- Retrospective cohort study of 2,259 STEMI patients undergoing primary PCI.
- Apo-B calculated using established equations from initial lipid measurements.
- High Apo-B defined as ≥65; primary endpoint was major adverse cardiovascular events (MACE).
Main Results:
- High Apo-B levels (≥65) were significantly associated with MACE (OR: 3.02; 95% CI: 1.07-8.47; p=0.036).
- Apo-B did not predict suboptimal TIMI flow (OR: 0.56; 95% CI: 0.17-1.87; p=0.349).
- LDL-C and Non-HDLC showed weaker predictive power for MACE compared to Apo-B.
Conclusions:
- Calculated Apo-B is a simple and effective tool for predicting cardiovascular events in STEMI patients.
- Apo-B demonstrates superior prognostic capability for MACE compared to LDL-C and Non-HDLC in this cohort.
Background:
Debates still surround using lipoproteins including Apo-B in risk assessment, management, and prognosis of patients with coronary artery disease. During an acute ST-segment elevation myocardial infarction, Apo-B might help to achieve incremental prognostic information.
Objective:
We sought to determine the potential prognostic utility of calculated Apo-B in a cohort of patients with STEMI undergoing primary PCI.
Methods:
A retrospective cohort study was conducted enrolling 2,259 patients with a diagnosis of acute STEMI who underwent primary PCI. Apo-B was obtained using a valid equation based on initial lipid measurements. High Apo-B was defined as a level of 65 or higher. Primary endpoint of the study was major adverse cardiovascular events (MACE).
Results:
Mean age of the participants was 59.54 years and 77.9% of them were male. After a Median follow up of 15 (6.2) months, high Apo-B was associated with MACE and the OR (95% CI) was 3.02 (1.07-8.47), p = .036. Odds ratios for prediction of MACE pertaining to LVEF, and smoking were 0.97 (p = .044), and 1.07 (p = .033), respectively. However, High Apo-B was not able to predict suboptimal TIMI flow. Accordingly, the Odds ratio was 0.56 (0.17-1.87), p = 0.349. The power of High LDL-C and Non-HDLC for prediction of MACE were assessed in distinct models. Attained odds ratios were [2.40 (0.90-6.36), p = .077] and [1.80 (0.75-4.35), p = 0.191], respectively.
Conclusion:
Calculated Apo-B appears to be a simple tool applicable for prediction of cardiovascular events in patients with STEMI superior to both Non-HDLC and LDL-C.
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