In HIV patients, statin therapy will attenuate plaque inflammation, thus, making plaques less vulnerable, will deter plaque progression, and improve endothelial function. In addition to known cholesterol-lowering and C-reactive protein lowering effects, immunomodulatory effects of statins will lead to a shift from pro-inflammatory monocyte and T cell subsets to less atherogenic subpopulations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
40
20 mg PO QD for the first 3 months, followed by 40 mg PO QD for the final 9 months.
Placebo
Massachusetts General Hospital
Boston, Massachusetts, United States
Coronary and Aortic Plaque Inflammation
12 month change in mean FDG-PET TBR (18-fluorodeoxyglucose positron emission tomography target-to-background ratio)
Time frame: Measured at baseline and 1 year
Plaque Progression
12 month percent change in plaque volume
Time frame: Measured at baseline and 1 year
Endothelial Function
Assessment of endothelial function was to be measured by endothelial vasodilator function.
Time frame: 1 year
Immune Function
12 month change in CD4 T-lymphocytes
Time frame: Measured at baseline and 1 year
Lipid Profile
12 month change in lipid profile
Time frame: Measured at baseline and 1 year
C-reactive Protein (CRP)
12 month change in Log CRP concentration
Time frame: Measured at baseline and 1 year
Adipocytokines
12 month change in IL-6
Time frame: Measured at baseline and 1 year
Liver Function Tests (LFTs)
Number of participants with LFT abnormalities (greater than or equal to 3 times the upper limit of normal). For reference, the normal ranges for AST and ALT are shown below. Please note that the normal range for ALT at Labcorp changed over the course of the study. AST and ALT elevations were determined based on the normal range at the time the lab test was performed. ALT: 0-40 IU/L, 0-44 IU/L, or 0-55 IU/L AST: 0-40 IU/L
Time frame: Measured at baseline, 1, 3, 6, 9, and 12 months
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