PSORIASIS Clinical Trial
Official title:
Etanercept and Vascular Function in Psoriasis
The investigators plan to measure the health of the vascular system of subjects taking Etanercept for the treatment of plaque psoriasis.
Psoriasis is a chronic disease that mainly affects the skin. The most common form of
psoriasis, plaque psoriasis, can appear anywhere on the body, but it is most commonly found
on the elbows, knees, scalp, and lower back. Skin typically becomes red and inflamed and may
form scaly patches. While psoriasis may look like just a skin disease, it is in fact a
result of an overacting, malfunctioning immune system. One consequence of this dysfunction
is over-activity of a substance called tumor necrosis factor (TNF). TNF alters the body's
immune response by promoting inflammation. High TNF activity is associated with psoriasis
and many other diseases of the immune system.
There are multiple treatments for psoriasis ranging from topical medications including
steroid creams, coal tar extracts, and exposure to UV light. For moderate to severe disease,
drugs that change how the immune system works are sometimes used. One of these drugs is
Etanercept, a prescription medicine approved by the FDA for the treatment of moderate to
severe plaque psoriasis. Etanercept works by reducing the amount of TNF in the body and
thereby reducing inflammation and keep skin clearer.
Inflammation appears on the skin of patients with psoriasis, but recent research has shown
that abnormal inflammation plays a role in the development of a disease of blood vessels
called atherosclerosis. Atherosclerosis is the build-up of plaques within arteries in the
body causing gradual narrowing and occasionally rupturing causing angina (chest pain), heart
attacks, strokes, and peripheral vascular disease. Many of the traditional risk factors for
atherosclerosis (including high blood pressure, diabetes, and smoking) are themselves
associated with increased inflammation.
These risk factors themselves also increase the production of certain molecules called
reactive oxygen species. Too many reactive oxygen species molecules results in a condition
called oxidative stress. Oxidative stress leads to abnormal function of the cells that line
the blood vessels, called endothelial cells, and this process promotes inflammation within
the blood vessel. Over time, this leads to irreversible damage to the heart and blood
vessels.
To counteract this damage, the body produces endothelial progenitor cells (EPCs) in the bone
marrow. The EPCs help balance out the damage that occurs in the blood vessels from oxidative
stress and other harmful processes. Several other drugs commonly used in heart disease have
recently been shown to improve EPCs function.
This balance of oxidative stress, inflammation, EPCs and the immune system is complex and
not fully understood. Drugs like Etanercept that modify the inflammatory response of the
immune system are useful not only as therapies for diseases like psoriasis, but can help
expand understanding of inflammation and arthrosclerosis.
The investigators plan to measure the health of the vascular system of subjects taking
Etanercept for the treatment of plaque psoriasis. To do that, we plan to take blood samples
to check for cardiovascular risk factors, inflammation levels, oxidative stress levels, and
EPCs. The investigators will also measure how well the arteries relax by ultrasound ( a
non-invasive test). Because we want to measure the effect of Etanercept on the blood vessels
we will have each subject take Etanercept for 3 months and a placebo injection for 3 months
checking ultrasound and blood tests at the end of each cycle.
Subjects in the study will all be individuals who would be eligible to receive Etanercept
under its current FDA use guidelines (for psoriasis). Our interest is in the potential
effects of this drug on the vascular system. By performing this study we hope to better
understand the interplay between vascular disease, inflammation and the immune system. If a
drug that modulates the inflammatory response causes changes in vascular function, it would
be an important step towards possible new avenues of treatment of cardiovascular disease.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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