Changes in the Lipidome Are Associated With Immune Activation and Subclinical Vascular Disease in Youth With Human Immunodeficiency Virus in Uganda

Sahera Dirajlal-Fargo*, Melica Nikahd, Kate Ailstock, Manjunath Manubolu, Victor Musiime, Cissy Kityo, Grace A. Mccomsey, Nicholas T. Funderburg*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Background: This study examined the changes in the lipidome and associations with immune activation and cardiovascular disease (CVD) markers in youth with perinatally acquired human immunodeficiency virus (YPHIV). Methods: The serum lipidome was measured in antiretroviral therapy (ART)-treated YPHIV (n = 100) and human immunodeficiency virus-uninfected children (n = 98) in Uganda. Plasma markers of systemic inflammation, monocyte activation, gut integrity, and T-cell activation, as well as common carotid artery intima media thickness and pulse wave velocity (PWV), were evaluated at baseline and 96 weeks. Results: Overall, median age was 12 years, and 52% were females. Total cholesterol, low-density lipoprotein (LDL), and high-density lipoprotein were similar between the groups; however, the concentrations of ceramides, diacylglycerols, free fatty acids, lysophosphatidylcholines, and phosphatidylcholines were higher in YPHIV (P ≤. 03). Increases in phosphatidylethanolamine (16:0 and 18:0) correlated with increases in soluble CD163, oxidized LDL, C-reactive protein, intestinal fatty acid binding protein, and PWV in YPHIV (r ≥ 0.3). Conclusions: YPHIV successfully suppressed on ART have elevated lipid species that are associated with CVD, specifically palmitic acid (C16:0) and stearic acid (C18:0).

Original languageEnglish (US)
Pages (from-to)403-413
Number of pages11
JournalJournal of Infectious Diseases
Volume231
Issue number2
DOIs
StatePublished - Feb 15 2025

Funding

Financial support. This work was supported by the National Institute of Allergy and Infectious Diseases and the Eunice Kennedy Shriver National Institute of Child Health (grant numbers U01 AI168630 to N. T. F. and S. D.-F., and R21HD106579 to S. D.-F.). This publication was made possible through funding support of University Hospitals Cleveland Medical Center Clinical Research Center (UHCRC) and the Clinical and Translational Science Collaborative of Cleveland (UL1TR002548) from the National Center for Advancing Translational Sciences component of the National Institutes of Health (NIH) and NIH Roadmap for Medical Research. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of UHCRC or the NIH.

Keywords

  • cardiovascular disease
  • immune activation
  • inflammation
  • lipids
  • perinatally acquired HIV

ASJC Scopus subject areas

  • General Medicine

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