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A borderline range for Quantiferon Gold In-Tube results
OBJECTIVE: Interferon gamma release assays like Quantiferon Gold In-Tube (QFT) are used to identify individuals infected with Mycobacterium tuberculosis. A dichotomous cut-off (0.35 IU/ml) defines a positive QFT without considering test variability. Our objective was to evaluate the introduction of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667766/ https://www.ncbi.nlm.nih.gov/pubmed/29095918 http://dx.doi.org/10.1371/journal.pone.0187313 |
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author | Jonsson, Jerker Westman, Anna Bruchfeld, Judith Sturegård, Erik Gaines, Hans Schön, Thomas |
author_facet | Jonsson, Jerker Westman, Anna Bruchfeld, Judith Sturegård, Erik Gaines, Hans Schön, Thomas |
author_sort | Jonsson, Jerker |
collection | PubMed |
description | OBJECTIVE: Interferon gamma release assays like Quantiferon Gold In-Tube (QFT) are used to identify individuals infected with Mycobacterium tuberculosis. A dichotomous cut-off (0.35 IU/ml) defines a positive QFT without considering test variability. Our objective was to evaluate the introduction of a borderline range under routine conditions. METHODS: Results of routine QFT samples from Sweden (2009–2014) were collected. A borderline range (0.20–0.99 IU/ml) was introduced in 2010 recommending a follow-up sample. The association between borderline results and incident active TB within 3 to 24 months was investigated through linkage with the national TB-register. RESULTS: Using the recommended QFT cut-off, 75.1% tests were negative, 21.4% positive and 3.5% indeterminate. In total, 9% (3656/40773) were within the borderline range. In follow-up samples, individuals with initial results between 0.20–0.34 IU/ml and 0.35–0.99 IU/ml displayed negative results below the borderline range (<0.20 IU/ml) in 66.1% (230/348) and 42.5% (285/671) respectively, and none developed incident TB. Among 6712 individuals with a positive initial test >0.99 IU/ml, 65 (0.97%) developed incident TB within 3–24 months. CONCLUSIONS: We recommend retesting of subjects with QFT results in the range 0.20–0.99 IU/ml to enhance reliability and validity of the test. Half of the subjects in the borderline range will be negative at a level <0.20 IU/ml when retested and have a very low risk of developing incident active TB. |
format | Online Article Text |
id | pubmed-5667766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56677662017-11-17 A borderline range for Quantiferon Gold In-Tube results Jonsson, Jerker Westman, Anna Bruchfeld, Judith Sturegård, Erik Gaines, Hans Schön, Thomas PLoS One Research Article OBJECTIVE: Interferon gamma release assays like Quantiferon Gold In-Tube (QFT) are used to identify individuals infected with Mycobacterium tuberculosis. A dichotomous cut-off (0.35 IU/ml) defines a positive QFT without considering test variability. Our objective was to evaluate the introduction of a borderline range under routine conditions. METHODS: Results of routine QFT samples from Sweden (2009–2014) were collected. A borderline range (0.20–0.99 IU/ml) was introduced in 2010 recommending a follow-up sample. The association between borderline results and incident active TB within 3 to 24 months was investigated through linkage with the national TB-register. RESULTS: Using the recommended QFT cut-off, 75.1% tests were negative, 21.4% positive and 3.5% indeterminate. In total, 9% (3656/40773) were within the borderline range. In follow-up samples, individuals with initial results between 0.20–0.34 IU/ml and 0.35–0.99 IU/ml displayed negative results below the borderline range (<0.20 IU/ml) in 66.1% (230/348) and 42.5% (285/671) respectively, and none developed incident TB. Among 6712 individuals with a positive initial test >0.99 IU/ml, 65 (0.97%) developed incident TB within 3–24 months. CONCLUSIONS: We recommend retesting of subjects with QFT results in the range 0.20–0.99 IU/ml to enhance reliability and validity of the test. Half of the subjects in the borderline range will be negative at a level <0.20 IU/ml when retested and have a very low risk of developing incident active TB. Public Library of Science 2017-11-02 /pmc/articles/PMC5667766/ /pubmed/29095918 http://dx.doi.org/10.1371/journal.pone.0187313 Text en © 2017 Jonsson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jonsson, Jerker Westman, Anna Bruchfeld, Judith Sturegård, Erik Gaines, Hans Schön, Thomas A borderline range for Quantiferon Gold In-Tube results |
title | A borderline range for Quantiferon Gold In-Tube results |
title_full | A borderline range for Quantiferon Gold In-Tube results |
title_fullStr | A borderline range for Quantiferon Gold In-Tube results |
title_full_unstemmed | A borderline range for Quantiferon Gold In-Tube results |
title_short | A borderline range for Quantiferon Gold In-Tube results |
title_sort | borderline range for quantiferon gold in-tube results |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667766/ https://www.ncbi.nlm.nih.gov/pubmed/29095918 http://dx.doi.org/10.1371/journal.pone.0187313 |
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