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Updated: Jun 20, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
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
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.
Abstract:
After reviewing the general characteristics of lipids (LDL-C, VLDL-C, HDL-C) and atherothrombosis, including the I-VIII degrees of its histopathological arterial lesions (with contributions of J. E. Edwards and R. Virmani), the authors described the P. Libby's data on lipoprotein-associated phospholipaseA2 (Lp-PLA2) and its two inflammatory mediators: lysophosphatidylcholine and oxidized nonesterified fatty acids. They are involved in plaque progression and vulnerability. Lp-PLA2 is an emerging proinflammatory marker. The new drug darapladib inhibits Lp-PLA2 and acts against inflammation. LDL-C is present in the atherosclerotic plaque from the circulating blood in arterial lumen (through the dysfunctional endothelium) and vasa vasorum as well as after the decomposition of foam cells (monocytes-phagocytes, smooth muscle and dendritic cells) and outpoured erythrocytes (its membranes) after hemorrhage. The blood from the arterial lumen can also enter the atherosclerotic plaque through the lesions in its fibrous cap (erosion, fissure, rupture). Atherosclerosis as a disease or as an inevitable accompaniment of aging ("the senescence hypothesis"). The familial hypercholesterolemia is usually due to mutation of just one gene--a defective LDL-C receptor gene on chromosome 19. The accelerated and severe atherosclerosis very resistant to therapy occurs. The patients with homozygous familial hypercholesterolemia can die of myocardial infarction in early childhood. Therapeutic decrease of LDL-C and increase of HDL-C slows down the evolution of atherosclerosis, stabilizes the atherosclerotic plaques, and even brings about their partial regression. Statins, niacin, ezetimibe, LDL-C apheresis, and surgery: shunt between the portal and inferior caval veins, liver transplantation, and partial ileal bypass. The elevated LDL-C is the most established risk factor for atherosclerosis with impact on coronary heart disease mortality of 26%, and it should be the primary target of preventive and therapeutic efforts.
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