Epidemiology
Lp(a) at or above 180 mg/dL nearly triples MACE risk even after LDL-C targets are met in diabetic ACS patients post-PCI (Sci Prog 2025)
Original title: Predictive value of Lp(a) for MACE in ACS patients with T2DM following PCI, with achieved LDL-C target: A cross-sectional study
In a retrospective study of 462 patients with acute coronary syndrome and type 2 diabetes who underwent percutaneous coronary intervention and achieved the recommended LDL-C target (1.4 mmol/L or below), patients were followed for a median 27 months for major adverse cardiovascular events (MACE, defined as all-cause death, recurrent myocardial infarction, ischaemic stroke, or hospitalisation for recurrent angina). Patients who developed MACE had more coronary lesions and significantly higher Lp(a). Those with Lp(a) at or above 180 mg/dL had a higher incidence of MACE and recurrent myocardial infarction than the other two Lp(a) groups, and after multivariate adjustment remained independently associated with increased MACE risk (hazard ratio 2.82, 95% CI 1.47-5.41, P = .002) and recurrent myocardial infarction (hazard ratio 3.71, 95% CI 1.17-11.81, P = .026). Elevated Lp(a) identifies substantial residual cardiovascular risk in diabetic ACS patients who have otherwise met LDL-C treatment goals.
Original abstract
ObjectiveIt is widely accepted that elevated low-density lipoprotein cholesterol (LDL-C) levels are a major risk factor for coronary heart disease (CHD). However, even patients who have achieved LDL-C levels below the currently recommended targets may still have residual risk. Recently, Lipoprotein(a) [Lp(a)] has attracted significant attention as independent causal risk factor for CHD. Nonetheless, the role of Lp(a) in acute coronary syndrome (ACS) patients with type 2 diabetes mellitus (T2DM) who have undergone percutaneous coronary intervention (PCI) and achieved the LDL-C target (≤1.4 mmol/L) remains unclear.MethodsThis retrospective study enrolled 462 ACS patients with comorbid T2DM who underwent PCI, with a median follow-up duration of 27 months post-procedure. The primary endpoint was major adverse cardiovascular events (MACE), defined as all-cause death, recurrent acute myocardial infarction (AMI), ischemic stroke, or hospitalization due to recurrent angina. Based on MACE occurrences, patients were divided into MACE group and non-MACE group. Furthermore, patients were further divided into three groups according to their Lp(a) levels. Kaplan-Meier and Cox regression analyses were performed.ResultsPatients with MACE had more coronary artery lesions, and the plasma Lp(a) concentrations in the MACE group were significantly higher than in the non-MACE group. The incidence of MACE and recurrent AMI was higher in the Lp(a) ≥ 180 mg/dL group compared to the other two groups. Even after multivariate adjustment, Lp(a) ≥ 180 mg/dL remained closely associated with an increased risk of MACE (HR 2.82, 95% CI: 1.47-5.41, P = .002) and recurrent AMI (HR 3.71, 95% CI: 1.17-11.81, P = .026).ConclusionElevated Lp(a) levels were strongly associated with poor prognosis in ACS patients with T2DM who underwent PCI.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.