Endothelial Dysfunction Is Related to Monocyte Activation in Antiretroviral-Treated People With HIV and HIV-Negative Adults in Kenya.

Africa HIV I-FABP antiretroviral therapy endothelial activation inflammation sCD14

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 19 06 2020
accepted: 10 09 2020
entrez: 23 10 2020
pubmed: 24 10 2020
medline: 24 10 2020
Statut: epublish

Résumé

Residual monocyte activation may contribute to increased risk for endothelial dysfunction and subsequent atherosclerotic cardiovascular diseases (CVDs) among people with HIV (PWH) on antiretroviral therapy (ART). We examined the relationship between monocyte activation and endothelial activation in PWH in Kenya. Serum levels of markers of endothelial activation (soluble/circulating intercellular [sICAM-1] and vascular [sVCAM-1] cell adhesion molecule-1), intestinal barrier dysfunction (intestinal fatty acid binding protein [I-FABP]), and monocyte activation (soluble CD14 [sCD14]) were measured in 275 PWH on ART and 266 HIV-negative persons. Linear regression was used to evaluate associations, adjusting for demographic and traditional CVD risk factors. Among 541 participants, the median age was 43 years, 50% were female, and most PWH were virally suppressed (97%). sICAM-1 and sVCAM-1 levels were significantly higher in PWH than in HIV-negative participants ( Despite viral suppression, African PWH have evidence of enhanced endothelial activation associated with sCD14, suggesting that monocyte activation plays a role in atherosclerotic plaque development. Future studies are needed to determine mechanistic pathways leading to monocyte activation in this population.

Sections du résumé

BACKGROUND BACKGROUND
Residual monocyte activation may contribute to increased risk for endothelial dysfunction and subsequent atherosclerotic cardiovascular diseases (CVDs) among people with HIV (PWH) on antiretroviral therapy (ART). We examined the relationship between monocyte activation and endothelial activation in PWH in Kenya.
METHODS METHODS
Serum levels of markers of endothelial activation (soluble/circulating intercellular [sICAM-1] and vascular [sVCAM-1] cell adhesion molecule-1), intestinal barrier dysfunction (intestinal fatty acid binding protein [I-FABP]), and monocyte activation (soluble CD14 [sCD14]) were measured in 275 PWH on ART and 266 HIV-negative persons. Linear regression was used to evaluate associations, adjusting for demographic and traditional CVD risk factors.
RESULTS RESULTS
Among 541 participants, the median age was 43 years, 50% were female, and most PWH were virally suppressed (97%). sICAM-1 and sVCAM-1 levels were significantly higher in PWH than in HIV-negative participants (
CONCLUSIONS CONCLUSIONS
Despite viral suppression, African PWH have evidence of enhanced endothelial activation associated with sCD14, suggesting that monocyte activation plays a role in atherosclerotic plaque development. Future studies are needed to determine mechanistic pathways leading to monocyte activation in this population.

Identifiants

pubmed: 33094120
doi: 10.1093/ofid/ofaa425
pii: ofaa425
pmc: PMC7568437
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofaa425

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : FIC NIH HHS
ID : R21 TW010459
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Tecla M Temu (TM)

Department of Global Health, University of Washington, Seattle, Washington, USA.

Stephen J Polyak (SJ)

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.

Jerry S Zifodya (JS)

Department of Medicine, Tulane University, New Orleans, Louisiana, USA.

Celestine N Wanjalla (CN)

Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.

John R Koethe (JR)

Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.

Sarah Masyuko (S)

Department of Global Health, University of Washington, Seattle, Washington, USA.

Jerusha Nyabiage (J)

Department of Global Health, University of Washington, Seattle, Washington, USA.

John Kinuthia (J)

Department of Global Health, University of Washington, Seattle, Washington, USA.
Kenyatta National Hospital, Nairobi, Kenya.

Ana L Gervassi (AL)

Center for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, Washington, USA.

Julius Oyugi (J)

Department of Medical Microbiology, University of Nairobi, Nairobi, Kenya.

Stephanie Page (S)

Division of Metabolism, Endocrinology and Nutrition, University of Washington, Seattle, Washington, USA.

Carey Farquhar (C)

Department of Global Health, University of Washington, Seattle, Washington, USA.

Classifications MeSH