Aortic Stenosis Clinical Trial
Official title:
Endothelial Progenitors in Aortic Stenosis: Association With Aortic Stenosis Progression, Severity, Symptoms and Left Ventricular Function Assessed by 2D Strain Echocardiography
There is a correlation between endothelial progenitor cells (stem cells) and stenosis of the aortic valve.
Degenerative aortic valve (AV) stenosis (AS) is the most common valvular disease and
increases in prevalence with age. Severe aortic valve stenosis accounts for considerable
disease and death, especially in older patients. Aortic valve stenosis is the primary
indication for valve replacement in western countries, and the number will only increase as
elderly people are a growing subpopulation. Measures to identify AV disease earlier, to
identify factors that influence disease progression and treat AV disease pharmacologically
or with less invasive approaches would be a significant improvement over the current
standard of care. These advances will only be possible with a better understanding the
mechanisms underlying valve development and disease. Preliminary data suggest a novel
pathophysiological concept for impaired valvular endothelial cells regeneration, leading to
the progression of age-associated calcific AV disease and a potential treatment target is
the disrupted endothelial cell layer of the valve leaflet.
The research objectives are:
1. To assess the number and function of endothelial progenitor cellss and apoptotic
endothelial progenitor cellss in patients with mild, moderate and severe aortic
stenosis.
2. To study the association between aortic stenosis progression, severity, symptoms and
left ventricular function and the number and function of circulating endothelia
progenitor cells. By understanding the correlation between valve severity, left
ventricular longitudinal function and endothelial progenitor cells we will indentify
high risk patients population that need early intervention. We hope to add new
information on the pathogenesis of aortic stenosis and to indentify factors that
predict disease progression.
;
Allocation: Non-Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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