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Discrepancy between the tuberculin skin test and the whole-blood interferon gamma assay for the diagnosis of latent tuberculosis infection in an intermediate tuberculosis-burden country

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dc.contributor.authorKang, YA-
dc.contributor.authorLee, HW-
dc.contributor.authorYoon, HI-
dc.contributor.authorCho, BL-
dc.contributor.authorHan, SK-
dc.contributor.authorShim, YS-
dc.contributor.authorYim, JJ-
dc.date.accessioned2024-08-08T01:50:34Z-
dc.date.available2024-08-08T01:50:34Z-
dc.date.created2023-07-25-
dc.date.created2023-07-25-
dc.date.issued2005-06-
dc.identifier.citationJAMA - Journal of the American Medical Association, Vol.293 No.22, pp.2756-2761-
dc.identifier.issn0098-7484-
dc.identifier.urihttps://hdl.handle.net/10371/208582-
dc.description.abstractContext A recently developed whole-blood interferon gamma (IFN-gamma) assay based on stimulation with the Mycobacterium tuberculosis-specific antigens early secreted antigenic target 6 and culture filtrate protein 10 shows promise for the diagnosis of latent tuberculosis (TB) infection. Objective To compare the tuberculin skin test (TST) and the whole-blood IFN-gamma assay in the diagnosis of latent TB infection according to the intensity of exposure. Design and Setting A prospective comparison between the whole-blood IFN-gamma assay and the TST using a 2-TU dose of purified protein derivative RT23 in a population with intermediate TB burden was conducted sequentially between February 1, 2004, and February 28, 2005, in a Korean tertiary referral hospital. Participants Of 273 participants, 220 (95.7%) had received BCG vaccine. Participants were grouped according to their risk of infection: group 1, no identifiable risk of M tuberculosis infection (n = 99); group 2, recent casual contacts (n = 72); group 3, recent close contacts (n = 48); group 4, bacteriologically or pathologically confirmed TB patients (n = 54). Main Outcome Measures Levels of agreement between the TST and the IFN-gamma assay and the likelihood of infection in the various groups. Results For the TST with a 10-mm induration cutoff, the positive response rate in group 1 was 51%; group 2, 60%; group 3, 71%, and group 4, 78%. For the IFN-gamma assay, the positive response rate in group 1 was 4%; group 2, 10%; group 3, 44%; and group 4, 81%. The overall agreement between the TST and the IFN-gamma assay in healthy volunteers was kappa = 0.16. The odds of a positive test result per unit increase in exposure across the 4 groups increased by a factor of 5.31 (95% confidence interval [01, 3.62-7.79) for the IFN-gamma assay and by a factor of 1.52 (95% Cl, 1.20-1.91) for the TST (P<.001). Using a 15-mm induration cutoff for the TST did not make a substantial difference to the test results. Conclusion The IFN-gamma assay is abetter indicator of the risk of M tuberculosis infection than TST in a BCG-vaccinated population.-
dc.language영어-
dc.publisherAmerican Medical Association-
dc.titleDiscrepancy between the tuberculin skin test and the whole-blood interferon gamma assay for the diagnosis of latent tuberculosis infection in an intermediate tuberculosis-burden country-
dc.typeArticle-
dc.identifier.doi10.1001/jama.293.22.2756-
dc.citation.journaltitleJAMA - Journal of the American Medical Association-
dc.identifier.wosid000229643700024-
dc.identifier.scopusid2-s2.0-20144384031-
dc.citation.endpage2761-
dc.citation.number22-
dc.citation.startpage2756-
dc.citation.volume293-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorCho, BL-
dc.contributor.affiliatedAuthorShim, YS-
dc.contributor.affiliatedAuthorYim, JJ-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCALMETTE-GUERIN VACCINATION-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusENUMERATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusESAT-6-
dc.subject.keywordPlusSCALE-
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  • College of Medicine
  • Department of Medicine
Research Area Nontuberculous Mycobacteria, Tuberculosis, multidrug-resistant tuberculosis, 결핵, 다제내성결핵, 비결핵항산균 폐질환

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