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dc.contributor.authorWinje, Brita Askeland
dc.contributor.authorWhite, Richard Aubrey
dc.contributor.authorSyre, Heidi
dc.contributor.authorSkutlaberg, Dag Harald
dc.contributor.authorOftung, Fredrik
dc.contributor.authorMengshoel, Anne Torunn
dc.contributor.authorBlix, Hege Salvesen
dc.contributor.authorBrantsæter, Arne Broch
dc.contributor.authorHolter, Ellen
dc.contributor.authorHandal, Nina
dc.contributor.authorSimonsen, Gunnar Skov
dc.contributor.authorAfset, Jan Egil
dc.contributor.authorKran, Anne-Marte Bakken
dc.date.accessioned2019-03-01T12:39:23Z
dc.date.available2019-03-01T12:39:23Z
dc.date.created2018-07-18T12:40:44Z
dc.date.issued2018
dc.identifier.citationThorax. 2018, 73 (7), 652-661.nb_NO
dc.identifier.issn0040-6376
dc.identifier.urihttp://hdl.handle.net/11250/2588271
dc.description.abstractIntroduction Targeted testing and treatment of latent TB infection (LTBI) are priorities on the global health agenda, but LTBI management remains challenging. We aimed to evaluate the prognostic value of the QuantiFERON TB-Gold (QFT) test for incident TB, focusing on the interferon (IFN)-γ level, when applied in routine practice in a low TB incidence setting. Methods In this large population-based prospective cohort, we linked QFT results in Norway (1 January 2009–30 June 2014) with national registry data (Norwegian Surveillance System for Infectious Diseases, Norwegian Prescription Database, Norwegian Patient Registry and Statistics Norway) to assess the prognostic value of QFT for incident TB. Participants were followed until 30 June 2016. We used restricted cubic splines to model non-linear relationships between IFN-γ levels and TB, and applied these findings to a competing risk model. Results The prospective analyses included 50 389 QFT results from 44 875 individuals, of whom 257 developed TB. Overall, 22% (n=9878) of QFT results were positive. TB risk increased with the IFN-γ level until a plateau level, above which further increase was not associated with additional prognostic information. The HRs for TB were 8.8 (95% CI 4.7 to 16.5), 19.2 (95% CI 11.6 to 31.6) and 31.3 (95% CI 19.8 to 49.5) times higher with IFN-γ levels of 0.35 to <1.00, 1.00 to <4.00 and >4.00 IU/mL, respectively, compared with negative tests (<0.35 IU/mL). Conclusions Consistently, QFT demonstrates increased risk of incident TB with rising IFN-γ concentrations, indicating that IFN-γ levels may be used to guide targeted treatment of LTBI.nb_NO
dc.language.isoengnb_NO
dc.publisherBMJ Publishing Groupnb_NO
dc.titleStratification by interferon-γ release assay level predicts risk of incident TBnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber652-661nb_NO
dc.source.volume73nb_NO
dc.source.journalThoraxnb_NO
dc.source.issue7nb_NO
dc.identifier.doi10.1136/thoraxjnl-2017-211147
dc.identifier.cristin1597783
dc.description.localcode© 2018. This is the authors' accepted and refereed manuscript to the article. The final authenticated version is available online at: http://dx.doi.org/10.1136/thoraxjnl-2017-211147nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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