HIV infection and high density lipoprotein metabolism
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Updated: Jul 9, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Honor Rose1, Jennifer Hoy, Ian Woolley
1Baker Heart Research Institute, Melbourne, Australia.
Insights
HIV infection alters high-density lipoprotein (HDL) metabolism, increasing cardiovascular disease risk. This study found dyslipidemia and impaired cholesterol transport in HIV-positive individuals, regardless of treatment.
Area of Science:
- Lipidology
- Virology
- Cardiovascular Medicine
Background:
- HIV infection and its treatments are linked to dyslipidemia and increased cardiovascular disease (CVD) risk.
- Understanding high-density lipoprotein (HDL) metabolism is crucial for managing CVD in HIV patients.
Purpose of the Study:
- To investigate HDL metabolism parameters in HIV-positive patients compared to HIV-negative controls.
- To assess the impact of HIV infection and antiretroviral therapy on lipid profiles and cholesterol transport.
Main Methods:
- Cross-sectional study comparing three groups: treatment-naïve HIV patients, HIV patients on protease inhibitors, and HIV-negative controls.
- Analysis of lipid parameters, including triglycerides, total cholesterol, LDL cholesterol, HDL cholesterol, apolipoproteins (apoB, apoA-I), lecithin cholesterol acyltransferase (LCAT), cholesteryl ester transfer protein (CETP), and phospholipid transfer protein (PLTP).
- Assessment of plasma's ability to promote cholesterol efflux and correlation analysis with CD4+ cell counts.
Main Results:
- HIV-infected patients, irrespective of treatment, showed elevated triglycerides, apoB, LCAT mass/activity, and CETP compared to controls.
- All HIV-infected groups exhibited lower HDL cholesterol and prebeta(1)-HDL.
- ApoA-I levels and cholesterol efflux capacity were similar across groups, but PLTP was reduced in treated patients. A positive correlation was observed between apoA-I and CD4+ cell counts.
Conclusions:
- HIV infection significantly alters HDL metabolism, characterized by dyslipidemia and impaired reverse cholesterol transport.
- These metabolic changes may contribute to the increased cardiovascular risk observed in HIV-positive individuals.
- Antiretroviral therapy may further impact specific HDL-related proteins like PLTP.
Abstract:
HIV infection and its treatment are associated with dyslipidemia, including hypoalphalipoproteinemia, and increased risk of cardiovascular disease. Parameters of HDL metabolism in HIV-positive patients were investigated in a cross-sectional study. The following groups of subjects were selected: (i) 25 treatment-naïve HIV-infected patients or HIV-infected patients on long therapy break, (ii) 28 HIV-infected patients currently treated with protease inhibitors, and (iii) 33 HIV-negative subjects. Compared to the HIV-negative group, all groups of HIV-infected patients were characterized by significantly elevated triglyceride and apolipoprotein B levels, mass and activity of lecithin cholesterol acyl transferase and cholesteryl ester transfer protein (p<0.01). Total and LDL cholesterol was lower in treatment-naïve HIV-infected group only. HDL cholesterol and prebeta(1)-HDL were significantly lower in all HIV-infected groups (p<0.05), while mean levels of apolipoprotein A-I (apoA-I) and ability of plasma to promote cholesterol efflux were similar in all groups. We found a positive correlation between apoA-I and levels of CD4+ cells (r(2)=0.3, p<0.001). Plasma level of phospholipid transfer protein was reduced in the group on antiretroviral therapy. Taken together these results suggest that HIV infection is associated with modified HDL metabolism re-directing cholesterol to the apoB-containing lipoproteins and likely reducing the functionality of reverse cholesterol transport.
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