Carotid Artery Stenosis Clinical Trial
Official title:
The Correlation Between the Enzyme Paraoxigenase 1 (PON1) to Carotid Artery Atheromatous Plaque
The objective of the research, is to examine the hypothesis, that the enzyme paraoxygenase 1 ( PON1) can influence carotid artery's atherosclerotic plaque content and stability, and its relation to plasma's enzyme concentration.
Atherosclerosis is a major risk factor for morbidity and mortality in the western world. It
is characterized by the accumulation of fat (cholesterol) in the arterial wall, creation of
the atheromatous plagues and the creation of arterial stenosis and occlusion. The cellular
content of theses plaques include: fibroblasts, endothelial cells, smooth muscle cells,
macrophages, and lipids: phospholipids, cholesterol, oxysterols and fatty acids. Lipids
penetration from the blood stream collaborates different proteins, including the
anti-atherogenic enzyme - paraoxygenase 1 - PON1. This enzyme has many ani-atherogenic
activities, e.g. Protection from oxygenation and increase of cholesterol efflux from
macrophages by HDL. Although the enzyme has a verity of substrates and known
anti-atherogenous function, its mechanism is still vogue. The enzymes accumulation rate is
the function of the advancement of the fatty strike towards advanced lesion. There is
evidence that the presence accumulation and activity of the PON1 within the plaque, is a
defense mechanism against atherosclerosis development. The assumption to be proved is that
PON1 can control plaque's content and influence its atherogenous factors. Furthermore, we
will try to identify these factors that the PON1 acts on. Beside plaque's content and PON1's
influence on them, we would like to investigate the phenotype of haptoglobin in the subjects
that the plaques were removed from. It is known that diabetics that have the genotype
haptoglobin 2-2, characterized by increased risk for oxygenation stress and cardiovascular
events (up to 5 times). We would like to examine if there is a correlation between plaque's
content, PON1's ability to disassemble oxygenized factors within the plaque, and the
phenotype to haptoglobin.
Methods: The plaque source will be from carotid endarterectomy, in the vascular unit. This
procedure is a routine operation for patients suffering from carotid artery stenosis, based
on clinical decisions. The plaques will be transported to a lipid laboratory soon after they
will be harvested, will be frozen in liquid nitrogen and processed into powder. This
material will be the origin for the proteins we try to extract. Patient's blood samples
(that is drawn routinely for the operation) will be the source for the characterization of
the haptoglobin's genotype.
It is critical to emphasize that routinely, the plaques are waste products, and only 5 cc of
additional blood is withdrawn from the patients for research purposes.
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Observational Model: Case Control, Time Perspective: Prospective
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