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dc.contributor.authorGraham, Susan M
dc.contributor.authorRajwans, Nimerta
dc.contributor.authorTapia, Kenneth A
dc.contributor.authorJaoko, Walter
dc.contributor.authorEstambale, Benson B.
dc.contributor.authorMcClelland, R. Scott
dc.contributor.authorOverbaugh, Julie
dc.contributor.authorLiles, W Conrad
dc.date.accessioned2018-06-28T07:11:36Z
dc.date.available2018-06-28T07:11:36Z
dc.date.issued2013
dc.identifier.urihttps://doi.org/10.1186/1471-2334-13-263
dc.identifier.urihttp://ir.jooust.ac.ke:8080/xmlui/handle/123456789/1343
dc.descriptionhttps://doi.org/10.1186/1471-2334-13-263en_US
dc.description.abstractBackground HIV-1-related inflammation is associated with increased levels of biomarkers of vascular adhesion and endothelial activation, and may increase production of the inflammatory protein angiopoietin-2 (ANG-2), an adverse prognostic biomarker in severe systemic infection. We hypothesized that antiretroviral therapy (ART) initiation would decrease endothelial activation, reducing plasma levels of ANG-2. Methods Antiretroviral-naïve Kenyan women with advanced HIV infection were followed prospectively. Endothelial activation biomarkers including soluble intercellular adhesion molecule-1 (ICAM-1), vascular adhesion molecule-1 (VCAM-1), and E-selectin, and plasma ANG-2 and angiopoietin-1 (ANG-1) were tested in stored plasma samples from 0, 6, and 12 months after ART initiation. We used Wilcoxon matched-pairs signed rank tests to compare endothelial activation biomarkers across time-points, generalized estimating equations to analyze associations with change in log10-transformed biomarkers after ART initiation, and Cox proportional-hazards regression to analyze associations with mortality. Results The 102 HIV-1-seropositive women studied had advanced infection (median CD4 count, 124 cells/μL). Soluble ICAM-1 and plasma ANG-2 levels decreased at both time-points after ART initiation, with concomitant increases in the beneficial protein ANG-1. Higher ANG-2 levels after ART initiation were associated with higher plasma HIV-1 RNA, oral contraceptive pill use, pregnancy, severe malnutrition, and tuberculosis. Baseline ANG-2 levels were higher among five women who died after ART initiation than among women who did not (median 2.85 ng/mL [inter-quartile range (IQR) 2.47–5.74 ng/mL] versus median 1.32 ng/mL [IQR 0.35–2.18 ng/mL], p = 0.01). Both soluble ICAM-1 and plasma ANG-2 levels predicted mortality after ART initiation. Conclusions Biomarkers of endothelial activation decreased after ART initiation in women with advanced HIV-1 infection. Changes in plasma ANG-2 were associated with HIV-1 RNA levels over 12 months of follow-up. Soluble ICAM-1 and plasma ANG-2 levels represent potential biomarkers for adverse outcomes in advanced HIV-1 infection.en_US
dc.language.isoenen_US
dc.publisherBioMed Central Ltd.en_US
dc.subjectHIVen_US
dc.subject1HAARTICAMen_US
dc.subject1VCAMen_US
dc.subject1Een_US
dc.subjectSelectinAngiopoietinen_US
dc.subject1Angiopoietinen_US
dc.subject2Endotheliumen_US
dc.titleA prospective study of endothelial activation biomarkers, including plasma angiopoietin-1 and angiopoietin-2, in Kenyan women initiating antiretroviral therapyen_US
dc.typeArticleen_US


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