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dc.contributor.authorFlygel, Trym Thune
dc.contributor.authorHameiri-Bowen, Dan
dc.contributor.authorSimms, Victoria
dc.contributor.authorRowland-Jones, Sarah
dc.contributor.authorFerrand, Rashida Abbas
dc.contributor.authorBandason, Tsitsi
dc.contributor.authorYindom, Louis-Marie
dc.contributor.authorOdland, Jon Øyvind
dc.contributor.authorCavanagh, Jorunn Pauline
dc.contributor.authorFlægstad, Trond
dc.contributor.authorSovershaeva, Evgeniya
dc.date.accessioned2023-12-21T09:57:21Z
dc.date.available2023-12-21T09:57:21Z
dc.date.issued2023-10-07
dc.description.abstractObjectives: Chronic lung disease is a recognized complication in children with HIV. Acute respiratory exacerbations (ARE) are common among this group and cause significant morbidity. Exhaled nitric oxide (eNO) is a known marker of local airway inflammation. We investigated the association between eNO and ARE, biomarkers of systemic inflammation, and the effect of azithromycin on eNO levels.<p> <p>Methods: Individuals aged 6–19 years with HIV-associated chronic lung disease in Harare, Zimbabwe, were enrolled in a placebo-controlled randomized trial investigating the effect of 48-week azithromycin treatment on lung function and ARE. eNO levels and biomarkers were measured at inclusion and after treatment in a consecutively enrolled subset of participants. Linear regression and generalized linear models were used to study associations between eNO and ARE, biomarkers, and the effect of azithromycin on eNO levels. <p>Results: In total, 172 participants were included in this sub-study, 86 from the placebo group and 86 from the azithromycin group. Participants experiencing at least one ARE during follow-up had significantly higher eNO levels at baseline than participants who did not (geometric mean ratio 1.13, 95% confidence interval [CI] 1.03–1.24, p = 0.015), adjusted for trial arm, age, sex and history of tuberculosis. Matrix metalloproteinase (MMP)-3, -7, and -10 were significantly associated with higher baseline eNO levels. At 48 weeks, azithromycin treatment did not affect eNO levels (geometric mean ratio 0.86, 95% CI 0.72– 1.03, p = 0.103). <p>Conclusion: Higher baseline eNO levels were a risk factor for ARE. eNO was associated with proinflammatory biomarkers previously found to contribute to the development of chronic lung disease. The potential use of eNO as a marker of inflammation and risk factor for ARE in HIV-associated chronic lung disease needs further investigation.en_US
dc.identifier.citationFlygel, Hameiri-Bowen, Simms, Rowland-Jones, Ferrand, Bandason, Yindom, Odland, Cavanagh, Flægstad, Sovershaeva. Exhaled nitric oxide is associated with inflammatory biomarkers and risk of acute respiratory exacerbations in children with HIV-associated chronic lung disease. HIV Medicine. 2023en_US
dc.identifier.cristinIDFRIDAID 2186604
dc.identifier.doi10.1111/hiv.13565
dc.identifier.issn1464-2662
dc.identifier.issn1468-1293
dc.identifier.urihttps://hdl.handle.net/10037/32193
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.ispartofFlygel, T.T. (2024). HIV Infected African Children: Gut microbiota in relation to chronic lung disease and long-term antibiotic treatment. (Doctoral thesis). <a href=https://hdl.handle.net/10037/33175>https://hdl.handle.net/10037/33175</a>.
dc.relation.journalHIV Medicine
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleExhaled nitric oxide is associated with inflammatory biomarkers and risk of acute respiratory exacerbations in children with HIV-associated chronic lung diseaseen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's license is described as Attribution 4.0 International (CC BY 4.0)