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Published on: October 12, 2017
Omega-3 fatty acids do not improve endothelial function in virologically suppressed HIV-infected men: a randomized
Corrilynn O Hileman1, Teresa L Carman, Norma J Storer
1Department of Medicine, Division of Infectious Diseases, MetroHealth Medical Center, Cleveland, Ohio, USA.
Insights
Omega-3 fatty acids did not improve endothelial function in adults with HIV. While inflammation markers showed a slight improvement, overall cardiovascular disease risk factors were not significantly impacted.
Area of Science:
- Cardiology
- Immunology
- Virology
Background:
- Cardiovascular disease (CVD) mortality may be reduced by omega-3 fatty acids, potentially via anti-inflammatory mechanisms.
- Inflammation and endothelial dysfunction are implicated in the elevated CVD risk observed in individuals with HIV.
- Stable antiretroviral therapy (ART) is crucial for managing HIV but may contribute to cardiovascular complications.
Purpose of the Study:
- To assess the impact of omega-3 fatty acids on endothelial function and inflammation in HIV-infected adults with moderate CVD risk.
- To determine if omega-3 supplementation can mitigate CVD risk factors in this population.
Main Methods:
- A 24-week, randomized, double-blind, placebo-controlled trial was conducted.
- Participants received omega-3-acid ethyl esters (1g twice daily) or a placebo.
- Key metrics included flow-mediated dilation (FMD), lipoproteins, and biomarkers for inflammation, endothelial activation, coagulation, and insulin resistance.
Main Results:
- No significant differences in the change of FMD were observed between the omega-3 and placebo groups.
- Lipoprotein levels and most biomarkers did not differ between groups.
- Soluble tumor necrosis factor receptor-I showed a trend favoring the omega-3 group, suggesting a potential anti-inflammatory effect.
Conclusions:
- Omega-3 fatty acids did not improve endothelial function, activation, coagulation, or insulin resistance in HIV-infected men on ART.
- A tendency towards improved inflammation markers was noted, but not sufficient to counteract HIV-related and ART-associated risks.
- Omega-3 fatty acids may not be potent enough to overcome the pro-inflammatory and endothelial dysfunction associated with HIV and its treatment.
Abstract:
Omega-3 fatty acids decrease cardiovascular disease (CVD) mortality possibly due to antiinflammatory effect. Inflammation and endothelial dysfunction likely play a role in the heightened CVD risk in HIV. Our goal was to evaluate the effect of omega-3 fatty acids primarily on endothelial function and inflammation in HIV-infected adults with moderate CVD risk on stable antiretroviral therapy. We conducted a 24-week, randomized, double-blind, placebo-controlled study to evaluate the effect of omega-3-acid ethyl esters 1 g twice a day. Flow-mediated dilation (FMD) of the brachial artery, lipoproteins and markers of inflammation, endothelial activation, coagulation, and insulin resistance were measured at entry and week 24. There were no within- or between-group differences in change in FMD over 24 weeks (mean change in FMD -0.13% vs. 1.5% for treatment vs. placebo; p=0.21). There were no between-group differences in changes in lipoprotein levels or biomarkers tested, except soluble tumor necrosis factor receptor-I, which favored omega-3-acid ethyl esters. Omega-3 fatty acids did not improve endothelial function or activation, coagulation, or insulin resistance in virologically suppressed, HIV-infected men with moderate CVD risk; however, inflammation tended to improve. This suggests that omega-3 fatty acids may not be potent enough to counteract the enhanced inflammation and endothelial dysfunction due to HIV and antiretrovirals.
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