Arterial stiffness is associated with oxidative stress and endothelial activation among persons with treated HIV in Zambia.

Oxidative stress arterial stiffness endothelial activation endothelial dysfunction peroxynitrite

Journal

Southern African journal of HIV medicine
ISSN: 2078-6751
Titre abrégé: South Afr J HIV Med
Pays: South Africa
ID NLM: 100965417

Informations de publication

Date de publication:
2021
Historique:
received: 12 08 2021
accepted: 24 09 2021
entrez: 3 12 2021
pubmed: 4 12 2021
medline: 4 12 2021
Statut: epublish

Résumé

Cardiovascular disease (CVD) prevalence is rising among persons with HIV (PLWH) in sub-Saharan Africa. Oxidative stress and endothelial activation, resulting in reduced vascular compliance, are contributors to CVD risk. However, there is a paucity of vascular health data in this population. To assess the relationships of oxidative stress and endothelial activation with vascular stiffness among PLWH. Fifty-four PLWH on antiretroviral therapy > 5 years and 57 HIV-negative controls, all aged 18-45 years, were enrolled from the University Teaching Hospital, Lusaka, Zambia. Oxidative stress was measured by nitrotyrosine, a peroxynitrite biomarker, and endothelial activation by soluble intercellular adhesion molecule-1 (sICAM-1) plasma levels. Vascular compliance was measured using carotid-radial pulse wave velocity (crPWV) and arterial stiffness index (crASI). PLWH had higher sICAM-1 levels (median 345 ng/mL) compared to controls (275 ng/mL, PLWH in sub-Saharan Africa had significantly greater oxidative stress and endothelial activation compared to HIV-negative individuals. These factors may contribute to increased arterial stiffness and higher CVD prevalence in this population.

Sections du résumé

BACKGROUND BACKGROUND
Cardiovascular disease (CVD) prevalence is rising among persons with HIV (PLWH) in sub-Saharan Africa. Oxidative stress and endothelial activation, resulting in reduced vascular compliance, are contributors to CVD risk. However, there is a paucity of vascular health data in this population.
OBJECTIVES OBJECTIVE
To assess the relationships of oxidative stress and endothelial activation with vascular stiffness among PLWH.
METHOD METHODS
Fifty-four PLWH on antiretroviral therapy > 5 years and 57 HIV-negative controls, all aged 18-45 years, were enrolled from the University Teaching Hospital, Lusaka, Zambia. Oxidative stress was measured by nitrotyrosine, a peroxynitrite biomarker, and endothelial activation by soluble intercellular adhesion molecule-1 (sICAM-1) plasma levels. Vascular compliance was measured using carotid-radial pulse wave velocity (crPWV) and arterial stiffness index (crASI).
RESULTS RESULTS
PLWH had higher sICAM-1 levels (median 345 ng/mL) compared to controls (275 ng/mL,
CONCLUSION CONCLUSIONS
PLWH in sub-Saharan Africa had significantly greater oxidative stress and endothelial activation compared to HIV-negative individuals. These factors may contribute to increased arterial stiffness and higher CVD prevalence in this population.

Identifiants

pubmed: 34858654
doi: 10.4102/sajhivmed.v22i1.1298
pii: HIVMED-22-1298
pmc: PMC8603157
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1298

Subventions

Organisme : NIAID NIH HHS
ID : K23 AI100700
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI110527
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024975
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW009744
Pays : United States
Organisme : NHLBI NIH HHS
ID : K01 HL130497
Pays : United States

Informations de copyright

© 2021. The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

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Auteurs

Theresa Chikopela (T)

Department of Physiology, Faculty of Medicine, Lusaka Apex Medical University, Lusaka, Zambia.

Fastone Goma (F)

Department of Physiological Sciences, School of Medicine, University of Zambia, Lusaka, Zambia.

Longa Kaluba (L)

School of Medicine, Cavendish University, Lusaka, Zambia.

Wilbroad Mutale (W)

Department of Health Policy and Management, School of Public Health, University of Zambia, Lusaka, Zambia.
Department of Internal Medicine, School of Medicine, University of Zambia, Lusaka, Zambia.

Chris Guure (C)

Department of Biostatistics, School of Public Health, University of Ghana, Legon, Ghana.

Douglas C Heimburger (DC)

Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.

John R Koethe (JR)

Division of Infectious Diseases, Vanderbilt University Medical Center, Vanderbilt University, Nashville, Tennessee, United States of America.

Classifications MeSH