Low and high density lipoprotein--cholesterol and coronary atherothrombosis

Vladimir Kanjuh1, Miodrag Ostojić, Nebojsa Lalić

  • 1Cardiovascular Pathology, University School of Medicine (Postgraduate), 11000 Belgrade, Dobracina 12. kanjuh@eunet.rs

Medicinski Pregled
|August 26, 2009
PubMed

Insights

Lowering LDL-C and raising HDL-C levels slows atherosclerosis progression and plaque instability. Elevated LDL-C is a primary risk factor for coronary heart disease mortality.

Area of Science:

  • Cardiovascular Science
  • Lipid Metabolism
  • Inflammation Biology

Background:

  • Atherosclerosis involves lipid accumulation, particularly LDL-C, within arterial walls, leading to plaque formation and potential rupture.
  • Lipoprotein-associated phospholipase A2 (Lp-PLA2) and its inflammatory mediators contribute to atherosclerotic plaque progression and vulnerability.

Discussion:

  • Familial hypercholesterolemia, often caused by LDL-C receptor gene defects, leads to severe, therapy-resistant atherosclerosis.
  • Dysfunctional endothelium and plaque cap lesions facilitate LDL-C entry into atherosclerotic plaques.
  • Atherosclerosis can be viewed as a disease process or an inevitable consequence of aging.

Key Insights:

  • Elevated LDL-C is the most significant risk factor for atherosclerosis, contributing to 26% of coronary heart disease mortality.
  • Therapeutic strategies including statins, niacin, ezetimibe, apheresis, and surgical interventions aim to reduce LDL-C and increase HDL-C.
  • New drugs like darapladib target Lp-PLA2, inhibiting inflammation and potentially stabilizing plaques.

Outlook:

  • Reducing LDL-C and increasing HDL-C are crucial for slowing atherosclerosis, stabilizing plaques, and promoting regression.
  • Targeting Lp-PLA2 offers a novel therapeutic avenue for managing inflammatory aspects of atherosclerosis.
  • Continued research into lipid management and anti-inflammatory strategies is vital for preventing cardiovascular events.

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