Why the study?
AIP is an established predictor of atherosclerosis and CAD, but whether it holds prognostic value for patients with premature coronary artery disease remained unclear.
Is the atherogenic index of plasma associated with major adverse cardiovascular events in patients with premature coronary artery disease?
Is the atherogenic index of plasma associated with major adverse cardiovascular events in patients with premature coronary artery disease?
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The atherogenic index of plasma is an independent prognostic marker for major adverse cardiovascular events in patients with premature coronary artery disease.
BACKGROUND: The atherogenic index of plasma (AIP) as a novel lipid biomarker has been shown to be an important predictor of atherosclerosis and coronary artery disease. However, it remains unclear whether AIP has prognostic value for patients with premature coronary artery disease (PCAD). Therefore, the present investigation aims to explore the relationship between AIP and major adverse cardiovascular events (MACE) in the PCAD population. METHODS: A total of 721 patients with PCAD diagnosed by coronary angiography were enrolled in this study. Their AIP was calculated as log [triglyceride (TG)/high-density lipoprotein-cholesterol (HDL-C)]. The primary outcome of this study was MACE, defined as a combination of cardiovascular (CV) death, coronary artery revascularization, non-fatal myocardial infarction (MI), and non-fatal stroke. RESULTS: After a median follow-up time of 52 months, 138 patients developed MACE. The patients in the highest AIP tertile group have a higher incidence of MACE (26.6% vs 11.8% and 19.8%, p < 0.001). The Kaplan-Meier curves demonstrated that there were significant differences in the risk of MACE among different AIP groups (log-rank p < 0.001). In addition, the multivariable Cox regression model showed that the hazard ratio of MACE in the highest tertile group was 2.27 (95% CI 1.30-3.94), and 1.33 (95% CI 1.06-1.67) for per SD increase in AIP. CONCLUSIONS: AIP is significantly associated with the risk of MACE in patients with PCAD and serves as a novel independent prognostic marker for this population.
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Ran et al. (2025) studied this question.
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