Overview
: Use of novel radio-pharmaceutical 64CUDOTA-ECL1i to evaluate arterial atherosclrosis
Description
Using 64CUDOTA-ECL1i to evaluate arterial atherosclrosis in normal volunteers and patients with carotid or femoral arterial atherosclerosis..
Eligibility
Inclusion Criteria: Normal Volunteers: 18-40 years of age, non smoker, no history of
diabetes, hypertension, or hyperlipidemia. Patients: 50-89 years of age, adequate
nutritional status, with or without smoking history, diabetes, hypertension, and
hyperlipidema. Both asymptomatic and symptomatic patients with known carotid artery
atherosclrosis >70% and scheduled to undergo surgery. Advanced peripheral artery disease.
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Exclusion Criteria:Inability to receive and sign informed consent. Currently enrolled in
another study. Patients who have type 1 diabetes or are in septic shock, receiving steroid
therapy, recent history of heavy alcohol consumption, (male >2 drinks per day, and female >
1 drink per day. following extreme diets like Atkins or South Beach diet or with Stage 4
chronic renal failure. Patients with unstable clinical condition that in the opinion of the
PI precludes participation in the study. Inability to tolerate 60 minutes in a supine
position with arms down at sides. Contraindications to MR imaging, (pacemaker, brain
aneurysm clips, shrapnel, etc. Positive pregnancy test or lactating. Have another
conditions such as cancer or autoimmune/inflammatory diseases, e.g. rheumatoid arthritis or
multiple sclerosis that are known to have increased expression of CCR2.
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