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Rapid Detection of Mycobacterium Tuberculosis Using a Novel Point-of-Care BZ TB/NTM NALF Assay: Integrating LAMP and LFIA Technologies

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dc.contributor.authorKim, Ha Nui-
dc.contributor.authorLee, Junmin-
dc.contributor.authorYoon, Soo-Young-
dc.contributor.authorJang, Woong Sik-
dc.contributor.authorLim, Chae Seung-
dc.date.accessioned2023-06-12T02:40:10Z-
dc.date.available2023-06-12T02:40:10Z-
dc.date.issued2023-04-
dc.identifier.issn2075-4418-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/63243-
dc.description.abstractTuberculosis (TB) is one of the leading causes of infectious mortality from a single infectious agent, Mycobacterium tuberculosis (MTB). This study evaluated the performance of the newly developed BZ TB/NTM NALF assay, which integrated loop-mediated isothermal amplification and lateral flow immunochromatographic assay technologies, for the detection of MTB. A total of 80 MTB-positive samples and 115 MTB-negative samples were collected, all of which were confirmed by TB real-time PCR (RT-PCR) using either AdvanSure (TM) TB/NTM RT-PCR Kit or Xpert((R)) MTB/RIF Assay. The performance of the BZ TB/NTM NALF assay was evaluated by calculating its sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) in comparison to those of the RT-PCR methods. Compared to the RT-PCR, the sensitivity, specificity, PPV, and NPV of BZ TB/NTM NALF assay were 98.7%, 99.1%, 98.7%, and 99.1%, respectively. The concordance rate between BZ TB/NTM NALF and RT-PCR was 99.0%. Rapid and simple detection of MTB is essential for global case detection and further elimination of TB. The performance of the BZ TB/NTM NALF Assay is acceptable with a high concordance with RT-PCR, indicating that it is reliable for use in a low-resource environment.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI AG-
dc.titleRapid Detection of Mycobacterium Tuberculosis Using a Novel Point-of-Care BZ TB/NTM NALF Assay: Integrating LAMP and LFIA Technologies-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/diagnostics13081497-
dc.identifier.scopusid2-s2.0-85153926481-
dc.identifier.wosid000979529300001-
dc.identifier.bibliographicCitationDiagnostics, v.13, no.8-
dc.citation.titleDiagnostics-
dc.citation.volume13-
dc.citation.number8-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusMEDIATED ISOTHERMAL AMPLIFICATION-
dc.subject.keywordPlusLABORATORY DIAGNOSIS-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusBIAS-
dc.subject.keywordAuthortuberculosis-
dc.subject.keywordAuthorTB-
dc.subject.keywordAuthorMTB-
dc.subject.keywordAuthorNALF-
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