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

Author:

Masenga Sepiso K.123,Elijovich Fernando4,Hamooya Benson M.15,Nzala Selestine6,Kwenda Geoffrey2,Heimburger Douglas C.3,Mutale Wilbroad7,Munsaka Sody M.2,Zhao Shilin8,Koethe John R.9,Kirabo Annet410

Affiliation:

1. School of Medicine and Health Sciences Mulungushi University Livingstone Zambia

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

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

4. Division of Clinical Pharmacology Vanderbilt University Medical Center Nashville TN

5. Department of Epidemiology and Biostatistics School of Public Health University of Zambia Lusaka Zambia

6. Department of Medical Education Development University of Zambia Lusaka Zambia

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

8. Department of Biostatistics Vanderbilt University Medical Center Nashville TN

9. Division of Infectious Diseases Vanderbilt University Medical Center Nashville TN

10. Department of Molecular Physiology and Biophysics Vanderbilt University Nashville TN

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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