Elevated Eosinophils as a Feature of Inflammation Associated With Hypertension in Virally Suppressed People Living With HIV.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
18 02 2020
Historique:
entrez: 18 2 2020
pubmed: 18 2 2020
medline: 15 12 2020
Statut: ppublish

Résumé

Background People living with HIV (PLWH) are at increased risk of cardiovascular disease, including hypertension, which persists despite effective plasma viral suppression on antiretroviral therapy. HIV infection is characterized by long-term alterations in immune function, but the contribution of immune factors to hypertension in PLWH is not fully understood. Prior studies have found that both innate and adaptive immune cell activation contributes to hypertension. Methods and Results We hypothesized that chronic inflammation may contribute to hypertension in PLWH. To test this hypothesis, we enrolled a cohort of 70 PLWH (44% hypertensive) on a long-term single antiretroviral therapy regimen for broad phenotyping of inflammation biomarkers. We found that hypertensive PLWH had higher levels of inflammatory cytokines, including tumor necrosis factor-α receptor 1, interleukin-6, interleukin-17, interleukin-5, intercellular adhesion molecule 1 and macrophage inflammatory protein-1α. After adjustment for age, sex, and fat mass index, the circulating eosinophils remained significantly associated with hypertension. On the basis of these results, we assessed the relationship of eosinophils and hypertension in 2 cohorts of 50 and 81 039 similar HIV-negative people; although eosinophil count was associated with prevalent hypertension, this relationship was abrogated by body mass index. Conclusions These findings may represent a unique linkage between immune status and cardiovascular physiological characteristics in HIV infection, which should be evaluated further.

Identifiants

pubmed: 32064996
doi: 10.1161/JAHA.118.011450
pmc: PMC7070208
doi:

Substances chimiques

Anti-Retroviral Agents 0
Cytokines 0
Inflammation Mediators 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e011450

Subventions

Organisme : FIC NIH HHS
ID : D43 TW009744
Pays : United States
Organisme : NIAID NIH HHS
ID : K23 AI100700
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002243
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI110527
Pays : United States
Organisme : NHLBI NIH HHS
ID : K01 HL130497
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Sepiso K Masenga (SK)

School of Medicine and Health Sciences Mulungushi University Livingstone Zambia.
Department of Biomedical Sciences School of Health Sciences University of Zambia Lusaka Zambia.
Vanderbilt Institute for Global Health Vanderbilt University Medical Center Nashville TN.

Fernando Elijovich (F)

Division of Clinical Pharmacology Vanderbilt University Medical Center Nashville TN.

Benson M Hamooya (BM)

School of Medicine and Health Sciences Mulungushi University Livingstone Zambia.
Department of Epidemiology and Biostatistics School of Public Health University of Zambia Lusaka Zambia.

Selestine Nzala (S)

Department of Medical Education Development University of Zambia Lusaka Zambia.

Geoffrey Kwenda (G)

Department of Biomedical Sciences School of Health Sciences University of Zambia Lusaka Zambia.

Douglas C Heimburger (DC)

Vanderbilt Institute for Global Health Vanderbilt University Medical Center Nashville TN.

Wilbroad Mutale (W)

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

Sody M Munsaka (SM)

Department of Biomedical Sciences School of Health Sciences University of Zambia Lusaka Zambia.

Shilin Zhao (S)

Department of Biostatistics Vanderbilt University Medical Center Nashville TN.

John R Koethe (JR)

Division of Infectious Diseases Vanderbilt University Medical Center Nashville TN.

Annet Kirabo (A)

Division of Clinical Pharmacology Vanderbilt University Medical Center Nashville TN.
Department of Molecular Physiology and Biophysics Vanderbilt University Nashville TN.

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