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Metabolic abnormalities and viral replication are associated with biomarkers of vascular dysfunction in HIV-infected
T I Miller1, W Borkowsky, L A DiMeglio
1Department of Pediatrics, Division of Pediatric Clinical Research, Miller School of Medicine at the University of Miami, Miami, FL, USA.
Insights
HIV-infected children show increased vascular dysfunction biomarkers compared to uninfected children. Unfavorable lipid profiles and active HIV replication are key risk factors for this heightened vascular dysfunction.
Area of Science:
- Pediatric cardiovascular health
- HIV/AIDS research
- Vascular biology
Background:
- Children with HIV may face premature cardiovascular disease.
- Understanding vascular dysfunction in pediatric HIV is crucial.
Purpose of the Study:
- To compare vascular dysfunction biomarkers in HIV-infected children versus HIV-exposed, uninfected (HEU) children.
- To identify factors associated with vascular dysfunction in HIV-infected children.
Main Methods:
- Prospective cohort study of 226 HIV-infected and 140 HEU children.
- Measured biomarkers of inflammation, coagulant, endothelial, and metabolic dysfunction.
- Collected data on anthropometry, body composition, lipids, glucose, insulin, HIV severity, and antiretroviral therapy.
Main Results:
- HIV-infected children exhibited higher levels of monocyte chemoattractant protein-1 (MCP-1), fibrinogen, soluble intracellular cell adhesion molecule-1 (sICAM), and soluble vascular cell adhesion molecule-1 (sVCAM).
- Higher levels of C-reactive protein (CRP) and fibrinogen were linked to lower BMI z-scores in HIV-infected children.
- Unfavorable lipid profiles and increased HIV viral load were associated with elevated inflammatory and endothelial dysfunction markers.
Conclusions:
- HIV-infected children demonstrate elevated biomarkers of vascular dysfunction compared to HEU children.
- Key risk factors include unfavorable lipid profiles and active HIV replication, highlighting the need for cardiovascular monitoring.
Objectives:
HIV-infected children may be at risk for premature cardiovascular disease. We compared levels of biomarkers of vascular dysfunction in HIV-infected children (with and without hyperlipidaemia) with those in HIV-exposed, uninfected (HEU) children enrolled in the Pediatric HIV/AIDS Cohort Study (PHACS), and determined factors associated with these biomarkers.
Methods:
A prospective cohort study was carried out. Biomarkers of inflammation [C-reactive protein (CRP), interleukin-6 (IL-6) and monocyte chemoattractant protein-1 (MCP1)], coagulant dysfunction (fibrinogen and P-selectin), endothelial dysfunction [soluble intracellular cell adhesion molecule-1 (sICAM), soluble vascular cell adhesion molecule-1 (sVCAM) and E-selectin], and metabolic dysfunction (adiponectin) were measured in 226 HIV-infected and 140 HEU children. Anthropometry, body composition, lipids, glucose, insulin, HIV disease severity, and antiretroviral therapy were recorded.
Results:
The median ages of the children were 12.3 years in the HIV-infected group and 10.1 years in the HEU group. Body mass index (BMI) z-scores, waist and hip circumferences, and percentage body fat were lower in the HIV-infected children. Total and non-high-density lipoprotein (HDL) cholesterol and triglycerides were higher in HIV-infected children. HIV-infected children also had higher MCP-1, fibrinogen, sICAM and sVCAM levels. In multivariable analyses in the HIV-infected children alone, BMI z-score was associated with higher CRP and fibrinogen, but lower MCP-1 and sVCAM. Unfavourable lipid profiles were positively associated with IL-6, MCP-1, fibrinogen, and P- and E-selectin, whereas increased HIV viral load was associated with markers of inflammation (MCP-1 and CRP) and endothelial dysfunction (sICAM and sVCAM).
Conclusions:
HIV-infected children have higher levels of biomarkers of vascular dysfunction than do HEU children. Risk factors associated with higher biomarkers include unfavourable lipid levels and active HIV replication.
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