We examined the impact of baseline high-density lipoprotein cholesterol efflux capacity (CEC) on major cardiac adverse events (MACE) in patients with coronary artery disease (CAD) during a long-term secondary prevention. Method: CEC was measured using a cell-based efflux system in (3)[H]-cholesterol-labeled J774 macrophages in apolipoprotein B-depleted plasma between January 2011 and January 2013. Patients with CAD were divided into 2 groups as a boundary CEC value of 1: 0.19 ≤ CEC 1 (impaired CEC group, mean CEC of 0.76 0.16, n 136), and 1 ≤ CEC ≤ 2.08 (enhanced CEC group, 1.20 0.19, n 44). MACE, comprised the incidence of cardiac death, non-fatal myocardial infarction, and any revascularizations (RV) without restenosis approximately 1 year after vascularization, was retrospectively investigated at September 2019. Impact of enhanced CEC on MACE among 22 variables was examined by applying a Cox proportional hazard model.
Result:The frequency of MACE in impaired CEC group (16.9%, mean observational interval of 2111 888 days) was significantly higher than that in enhanced CEC group (2.3%, 2,252 685, p 0.013), largely driven by the significantly higher RV incidence (14.0 % versus 2.3 %, p 0.032). Enhancement of CEC was the significant predictor of MACE (hazard ratio: 0.11; 95% CI: 0.013-0.879; p 0.038).
Conclusion:A baseline CEC level of more than 1 in patients with CAD brought favorable long-term clinical outcomes, suggesting that CEC is a useful prognostic and therapeutic surrogate for secondary prevention of CAD.apy of LDL-C 1) . Among the pleiotropic atheroprotective effects of high-density lipoprotein cholesterol (HDL-C), cholesterol efflux from macrophage (cholesterol efflux capacity, CEC) was consistently demonstrated as a negative predictor of CAD, independent of HDL-C and LDL-C levels 2, 3) . In addition, the CEC in asymptomatic healthy subjects predicts the incidence of atherosclerotic cardiovascular events