The main aims of this study are to determine whether: a) psoriasis patients with or without arthritis have more cardiovascular inflammation than healthy subjects and b)3 months of etanercept (enbrel) therapy (prescribed to psoriasis patients with or without arthritis by their treating clinicians) will decrease cardiovascular inflammation.
Psoriasis is a common disease characterized by skin lesions and systemic inflammation with or without arthritis. Patients with psoriasis have a higher risk of cardiovascular disease than healthy subjects, and this may be related in part to the inflammatory nature of their disease. This study is intended to help provide explanations for the increased cardiovascular disease risk in psoriasis and to assess whether this risk can be reduced by biologic anti-inflammatory therapies prescribed to resolve skin lesions and arthritis.
Study Type
OBSERVATIONAL
Enrollment
29
Massachusetts General Hospital
Boston, Massachusetts, United States
Aortic/coronary target to background ratio (TBR) on cardiac FDG-PET.
Degree of aortic/coronary atherosclerotic plaque inflammation assessed via cardiac FDG-PET as target to background ratio (TBR) of the standardized uptake value (SUV).
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Aortic/coronary atherosclerotic plaque burden on MDCT coronary angiography.
Burden of aortic/coronary atherosclerotic plaque as measured by MDCT coronary angiography.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Aortic/coronary atherosclerotic plaque morphology on MDCT coronary angiography.
Morphology of the aortic/coronary atherosclerotic plaque (e.g. calcification score, vulnerability characteristics) as measured by MDCT coronary angiography.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Endothelial function as measured by flow-mediated vasodilation.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Oral glucose tolerance.
Blood sugar and insulin levels during a standard 2-hour oral glucose tolerance test.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Lipid and lipoprotein levels.
Levels of total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, apolipoprotein A1, apolipoprotein B, apolipoprotein C-II, apolipoprotein C-III, and apolipoprotein E.
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Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Inflammatory biomarker levels.
Levels of inflammatory biomarkers including but not limited to high-sensitivity C-reactive protein, interleukin-6, and TNF-alpha.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).
Body fat distribution.
Measurements of height, weight, waist-to-hip ratio, leg circumference, arm circumference, and neck circumference. Determinations by whole body DEXA scanning of the total body and regional percent fat and lean body mass. Determination by single-slice abdominal computed tomography of total fat area, visceral adipose tissue, and subcutaneous adipose tissue.
Time frame: Baseline in all subjects and change from baseline to 3 months in psoriasis cohort starting etanercept (enbrel).