The HDL anti-inflammatory function is impaired in myocardial infarction and may predict new cardiac events independent of HDL cholesterol

  • Robin P. F. Dullaart*
  • , Wijtske Annema
  • , Rene A. Tio
  • , Uwe J. F. Tietge
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    36 Citations (Scopus)

    Abstract

    Background: Intrinsic functional properties of high density lipoproteins (HDL) are considered to be physiologically important for atheroprotection. We compared the HDL anti-inflammatory capacity between patients with acute myocardial infarction (MI) and patients with non-cardiac chest pain, and prospectively determined the association of new major adverse cardiovascular events (MACE) with this metric of HDL function.

    Methods: A prospective study was carried out in 93 patients referred for acute chest pain (65 patients with acute MI). The HDL anti-inflammatory capacity was determined as the ability to suppress tumor necrosis factor-alpha-induced vascular cell adhesion molecule-1 mRNA expression in endothelial cells in vitro.

    Results: Acute MI at admission was associated with impaired HDL anti-inflammatory capacity (p = 0.001), even after adjustment for HDL cholesterol and apolipoprotein A-I (p = 0.003). Twenty nine MACE were ascertained during a median follow-up of 1210 (910-1679) days. New MACE was associated with impaired HDL anti-inflammatory capacity (hazard ratio: 1.80 (1.17-2.77) per SD change, p = 0.007) in age, sex, HDL cholesterol and apolipoprotein-AI adjusted analysis.

    Conclusions: The ability of HDL to attenuate endothelial inflammation is impaired in acute MI, and this metric of HDL function may serve as a predictor of new MACE, even independent of HDL cholesterol and apolipoprotein A-I. (C) 2014 Elsevier B.V. All rights reserved.

    Original languageEnglish
    Pages (from-to)34-38
    Number of pages5
    JournalClinica chimica acta
    Volume433
    DOIs
    Publication statusPublished - 10-Jun-2014

    Keywords

    • Acute coronary syndrome
    • Atypical chest pain
    • HDL anti-inflammatory function
    • STEMI
    • Non-STEMI
    • HIGH-DENSITY-LIPOPROTEIN
    • ACUTE CORONARY SYNDROME
    • THERAPEUTIC TARGET
    • CHEST-PAIN
    • EFFLUX
    • ATHEROSCLEROSIS
    • MORTALITY
    • CAPACITY
    • DISEASE
    • RISK

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