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Recurrence of cardiovascular events despite achieving LDL-C <1.4 mmol/L in patients with coronary artery disease

Yu Kataoka1, Stephen J Nicholls2, Satoshi Kitahara3

  • 1Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center (Kataoka, Katasako-Yabumoto, Mitsui, Murai, Iwai, Sawada, Matama, Honda, Takagi, Fujino, Yoneda, Nakao, Asaumi, and Noguchi), Osaka, Japan.

Insights

Even with low-density lipoprotein cholesterol (LDL-C) below 1.4 mmol/L, patients with coronary artery disease (CAD) face ongoing risks. Achieving LDL-C below 1.0 mmol/L may further reduce major adverse cardiovascular events (MACE).

Area of Science:

  • Cardiology
  • Vascular Medicine
  • Clinical Research

Background:

  • European Society of Cardiology guidelines recommend LDL-C <1.4 mmol/L for very high-risk patients to prevent atherosclerotic cardiovascular disease (ASCVD).
  • Despite achieving target LDL-C levels, atherosclerosis progression and subsequent cardiovascular events remain a concern.
  • Coronary artery disease (CAD) patients require further risk stratification beyond LDL-C levels.

Purpose of the Study:

  • To investigate the clinical characteristics of CAD patients experiencing ASCVD events despite achieving LDL-C <1.4 mmol/L.
  • To identify predictors of major adverse cardiovascular events (MACE) in this patient cohort.
  • To evaluate the impact of achieving lower on-treatment LDL-C levels (<1.0 mmol/L) on MACE.

Main Methods:

  • Retrospective analysis of 780 CAD patients who achieved LDL-C <1.4 mmol/L post-percutaneous coronary intervention.
  • Comparison of clinical demographics between patients with and without MACE (cardiac death, MI, revascularization).
  • Multivariate analysis to identify independent predictors of MACE, including polyvascular disease (PVD) and on-treatment LDL-C levels.

Main Results:

  • MACE occurred in 6.2% of patients during a median follow-up of 1632 days.
  • Patients with MACE were significantly more likely to have PVD (72.9% vs 17.3%) and less likely to receive ezetimibe (45.8% vs 63.2%).
  • Lower on-treatment LDL-C <1.0 mmol/L was associated with reduced MACE risk (HR=0.37), particularly in patients with PVD (HR=0.36).

Conclusions:

  • Achieving LDL-C <1.4 mmol/L does not eliminate cardiovascular risk in CAD patients.
  • Polyvascular disease is a significant predictor of MACE in this population.
  • A more stringent LDL-C goal (<1.0 mmol/L) may be beneficial for preventing recurrent ASCVD events, especially in patients with PVD.
Abstract

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