Key result
Atorvastatin decreased serum oxLDL by 22.7% compared to a 7.5% increase with placebo (P<0.0001) in HIV patients, which correlated with improvements in coronary atherosclerosis.
Why the study?
Does atorvastatin reduce serum oxLDL levels and coronary plaque in HIV-infected patients with subclinical atherosclerosis?
RCT (n=40)
placebo-controlled
randomized
Does atorvastatin reduce serum oxLDL levels and coronary plaque in HIV-infected patients with subclinical atherosclerosis?
Atorvastatin significantly reduces serum oxLDL levels in HIV-infected patients, which correlates with reductions in high-risk coronary plaque features.
Atorvastatin lowers oxLDL in HIV patients with subclinical atherosclerosis; extends RCT evidence for statin effects on atherogenic lipids in this population.
OBJECTIVE: Circulating oxidized low-density lipoprotein (oxLDL) levels are elevated in HIV-infected patients and have been associated with atherosclerosis. Statins have been shown to reduce plaque on coronary computed tomography angiography (cCTA) in HIV-infected individuals. Thus, we investigated the effect of statins on serum oxLDL levels and the relationship between changes in oxLDL and coronary atherosclerosis on cCTA in patients with HIV. DESIGN: We previously conducted a 12-month randomized, placebo-controlled trial with atorvastatin in 40 HIV-infected patients on stable antiretroviral therapy with subclinical coronary atherosclerosis and low-density lipoprotein (LDL)-cholesterol less than 130 mg/dl. METHODS: In the current analysis, patients underwent cCTA and measurements of serum oxLDL, sCD14, sCD163, lipoprotein phospholipase-A2, and fasting lipids at baseline and end of the study. RESULTS: Nineteen patients were randomized to atorvastatin and 21 patients to placebo. Serum oxLDL decreased -22.7% (95% CI -28.7 to -16.7) in the atorvastatin group and increased 7.5% (95% CI -3.3 to 18.4) in the placebo group (P < 0.0001). Change in oxLDL significantly correlated with changes in noncalcified plaque volume, total plaque volume, positively remodeled plaque, and low attenuation plaque. The association between changes in oxLDL and noncalcified plaque volume was independent of the baseline 10-year Framingham risk, LDL, CD4 cell count, and viral load. CONCLUSION: Statins lower oxLDL levels in HIV-infected patients, and reductions in oxLDL are related to improvements in coronary atherosclerosis, independent of traditional cardiovascular risk factors. Reductions in oxLDL may be one mechanism through which statins exert beneficial effects on reducing atherosclerosis in HIV-infected individuals.
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Nou et al. (2015) conducted an RCT in HIV with subclinical coronary atherosclerosis (n=40). Atorvastatin vs. Placebo was evaluated on Change in serum oxLDL levels (p=< 0.0001). Atorvastatin decreased serum oxLDL by 22.7% compared to a 7.5% increase with placebo (P<0.0001) in HIV patients, which correlated with improvements in coronary atherosclerosis.
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