Positron emission tomography in the prediction of inflammation in children with human immunodeficiency virus related bronchiectasis

dc.contributor.authorMasekela, Refiloe
dc.contributor.authorGongxeka, Harlem
dc.contributor.authorGreen, Robin J.
dc.contributor.authorSathekge, Mike Machaba
dc.contributor.emailmike.sathekge@up.ac.zaen_US
dc.date.accessioned2012-05-31T14:27:25Z
dc.date.available2012-05-31T14:27:25Z
dc.date.issued2012-01
dc.description.abstractThere is a lack of objective tools to reliably diagnose exacerbations in bronchiectasis. The primary aim of this study was to assess the ability of fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) to detect sites of active inflammation in children with human immunodeficiency virus (HIV)-related bronchiectasis with or without exacerbations. The secondary aim was to assess whether 18F-FDG-PET/CT results are in agreement with local and systemic inflammatory markers and markers of HIV disease activity. Forty-one children with HIV-related bronchiectasis underwent 18F-FDG PET/CT. Data on the presence of a clinical exacerbation were recorded. Serum was collected for CD4 count, HIV viral load, C-reactive protein (CRP) and cytokines IL-8, INF-γ and TNF-α. Induced sputum samples were processed for microbiological culture and for IL-8, INF-γ and TNF-α. Mean age of all children was 8.2±2.2 years. Twelve subjects showed 18F-FDG lung uptake while six of them had an exacerbation. There was no difference in the 18F-FDG uptake in participants with or without an exacerbation (P=0.613). Fluorine- 18-FDG-PET had a good correlation with the presence of consolidation (P=0.01, OR=6.67). The mean CRP was higher in the subjects with 18F-FDG uptake when compared to those without uptake (51.96±95.12 vs. 13.26±19.87), although this difference was not significant (P=0.09). In conclusion, the 18F-FDG-PET technique could not reliably predict the presence of an exacerbation in children with HIV, and its diagnostic value was limited to identifying disease activity on the scan in acute pneumonia cases. Fluorine-18-FDG-PET had no significant correlation with CRP (or) with other inflammatory biomarkers and markers of HIV disease activity.en_US
dc.description.sponsorshipFunding for this study was partially obtained from the Research Development Programme fund of the University of Pretoria awarded to RM.en_US
dc.description.urihttp://www.nuclmed.gren_US
dc.identifier.citationMasekela, R, Gongxeka, H, Green, RJ & Sathekge, M 2012, 'Positron emission tomography in the prediction of inflammation in children with human immunodeficiency virus related bronchiectasis', Hellenic Journal of Nuclear Medicine, vol. 15, no. 1, pp.23-27.en_US
dc.identifier.issn1790-5427
dc.identifier.urihttp://hdl.handle.net/2263/19037
dc.language.isoenen_US
dc.publisherHellenic Society of Nuclear Medicineen_US
dc.rights© Hellenic Society of Nuclear Medicine 2011.en_US
dc.subjectBronchiectasisen_US
dc.subjectExacerbationsen_US
dc.subject18F-FDG PET scanen_US
dc.subjectCytokinesen_US
dc.subjectHuman immunodeficiency virus (HIV)en_US
dc.titlePositron emission tomography in the prediction of inflammation in children with human immunodeficiency virus related bronchiectasisen_US
dc.typePostprint Articleen_US

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