Abstract
Background. Among antiretroviral therapy (ART)–treated people with human immunodeficiency virus (PWH), persistent systemic immune activation contributes to atherogenesis atherosclerotic, cardiovascular disease (CVD) events, and mortality. Factors associated with key immune activation indices have not previously been characterized among a global primary CVD prevention cohort of PWH. Methods. Leveraging baseline Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) data, we evaluated factors associated with soluble CD14 (sCD14) and oxidized low-density lipoprotein (oxLDL). Results. The primary analysis cohort included 4907 participants from 5 global-burden-of-disease regions (38% female, 48% Black, median age 50 years). In fully adjusted models for sCD14, female sex and White race (among those in high-income regions) were associated with higher sCD14 levels, while higher body mass index (BMI) and current use of nucleoside reverse transcriptase inhibitor + integrase strand transfer inhibitor ART were associated with lower sCD14 levels. In fully adjusted models for oxLDL, male sex, residence in high-income regions, White race (among those in high-income regions), and higher BMI were associated with higher oxLDL levels. In a subanalysis cohort of 1396 women with HIV, increased reproductive age was associated with higher sCD14 levels but not with higher oxLDL levels. Conclusions. Factors associated with sCD14 and oxLDL, 2 key indices of immune-mediated CVD risk, differ. Future studies will elucidate ways in which medications (eg, statins) and behavioral modifications influence sCD14 and oxLDL and the extent to which dampening of these markers mediates CVD-protective effects.
| Original language | English |
|---|---|
| Pages (from-to) | 1324-1333 |
| Number of pages | 10 |
| Journal | Clinical Infectious Diseases |
| Volume | 75 |
| Issue number | 8 |
| DOIs | |
| State | Published - Oct 15 2022 |
Bibliographical note
Publisher Copyright:© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America.
Funding
Financial support. This work was supported through NIH, National Institute of Heart, Lung, and Blood Institute grants U01HL123336 to the Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) Clinical Coordinating Center and U01HL123339 to the REPRIEVE Data Coordinating Center, as well as through funding from ViiV Healthcare, Kowa Pharmaceuticals America, Inc, and Gilead Sciences. NIAID has supported this study through grants UM1 AI068636, which supports the ACTG Leadership and Operations Center, and UM1 AI106701, which supports the ACTG Laboratory. This work was also supported by NIH, NIAID grant R01AI123001 (to M. V. Z. and S. E. L.).
| Funders | Funder number |
|---|---|
| Gilead Sciences | |
| National Institutes of Health (NIH) | |
| National Heart, Lung, and Blood Institute (NHLBI) | U01HL123339, U01HL123336 |
| ACTG Leadership and Operations Center | UM1 AI106701, R01AI123001 |
| National Institute of Allergy and Infectious F32-AI286447 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI168214 Jason W. Rosch Diseases National Institute of Allergy and Infectious P30 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R00-AI166116 Christopher D. Radka Diseases National Institute of Allergy and Infectious T32-AI106700 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI192221 Jason W. Rosch Diseases National Inst... | UM1 AI068636 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- HIV
- cardiovascular disease risk
- immune activation markers
- reproductive aging
- women
ASJC Scopus subject areas
- Microbiology (medical)
- Infectious Diseases
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