Files in this item
Accuracy of the tuberculosis molecular bacterial load assay to diagnose and monitor response to anti-tuberculosis therapy : a longitudinal comparative study with standard-of-care smear microscopy, Xpert MTB/RIF Ultra, and culture in Uganda
Item metadata
dc.contributor.author | Musisi, Emmanuel | |
dc.contributor.author | Wamutu, Samuel | |
dc.contributor.author | Ssengooba, Willy | |
dc.contributor.author | Kasiinga, Sharifah | |
dc.contributor.author | Sessolo, Abdulwahab | |
dc.contributor.author | Sanyu, Ingvar | |
dc.contributor.author | Kaswabuli, Sylvia | |
dc.contributor.author | Zawedde, Josephine | |
dc.contributor.author | Byanyima, Patrick | |
dc.contributor.author | Kia, Praiscillia | |
dc.contributor.author | Muwambi, William | |
dc.contributor.author | Toskin, Divine Tracy | |
dc.contributor.author | Kigozi, Edgar | |
dc.contributor.author | Walbaum, Natasha | |
dc.contributor.author | Dombay, Evelin | |
dc.contributor.author | Legrady, Mate Bonifac | |
dc.contributor.author | Ssemambo, Kizza David-Martin | |
dc.contributor.author | Joloba, Moses | |
dc.contributor.author | Kuchaka, Davis | |
dc.contributor.author | Worodria, William | |
dc.contributor.author | Huang, Laurence | |
dc.contributor.author | Gillespie, Stephen H | |
dc.contributor.author | Sabiiti, Wilber | |
dc.date.accessioned | 2024-04-04T09:30:07Z | |
dc.date.available | 2024-04-04T09:30:07Z | |
dc.date.issued | 2024-04 | |
dc.identifier | 295491613 | |
dc.identifier | d635465f-bfb8-4913-a378-d45872458de6 | |
dc.identifier | 38458206 | |
dc.identifier | 38458206 | |
dc.identifier | 85186638380 | |
dc.identifier.citation | Musisi , E , Wamutu , S , Ssengooba , W , Kasiinga , S , Sessolo , A , Sanyu , I , Kaswabuli , S , Zawedde , J , Byanyima , P , Kia , P , Muwambi , W , Toskin , D T , Kigozi , E , Walbaum , N , Dombay , E , Legrady , M B , Ssemambo , K D-M , Joloba , M , Kuchaka , D , Worodria , W , Huang , L , Gillespie , S H & Sabiiti , W 2024 , ' Accuracy of the tuberculosis molecular bacterial load assay to diagnose and monitor response to anti-tuberculosis therapy : a longitudinal comparative study with standard-of-care smear microscopy, Xpert MTB/RIF Ultra, and culture in Uganda ' , The Lancet Microbe , vol. 5 , no. 4 , pp. e345-e354 . https://doi.org/10.1016/S2666-5247(23)00367-1 | en |
dc.identifier.issn | 2666-5247 | |
dc.identifier.other | ORCID: /0000-0001-6537-7712/work/156627349 | |
dc.identifier.other | ORCID: /0000-0002-4742-2791/work/156627514 | |
dc.identifier.uri | https://hdl.handle.net/10023/29599 | |
dc.description | Funding: Emmanuel Musisi’s doctoral research was supported by the European and Developing Countries Clinical Trial Partnership (EDCTP)-funded PanACEA II studentship (grant number TR1A2015-1102) and the University of St Andrews St Leonards scholarship. Funding from Makerere University Research and Innovation Fund (MAKRIF) by the Government of Uganda to Emmanuel Musisi and Samuel Wamutu supported collection and processing of specimens. Enrolment was funded by NIH R01 HL128156 and NIH R01 HL143998 grants. | en |
dc.description.abstract | BACKGROUND: In 2018, the tuberculosis molecular bacterial load assay (TB-MBLA), a ribosomal RNA-based test, was acknowledged by WHO as a molecular assay that could replace smear microscopy and culture for monitoring tuberculosis treatment response. In this study, we evaluated the accuracy of TB-MBLA for diagnosis and monitoring of treatment response in comparison with standard-of-care tests. METHODS: For this longitudinal prospective study, patients aged 18 years or older with presumptive tuberculosis (coughing for at least 2 weeks, night sweats, and weight loss) were enrolled at China-Uganda Friendship Hospital Naguru (Kampala, Uganda). Participants were evaluated for tuberculosis by TB-MBLA in comparison with Xpert MTB/RIF Ultra (Xpert-Ultra) and smear microscopy, with Mycobacteria Growth Indicator Tube (MGIT) culture as a reference test. Participants who were positive on Xpert-Ultra were enrolled on a standard 6-month anti-tuberculosis regimen, and monitored for treatment response at weeks 2, 8, 17, and 26 after initiation of treatment and then 3 months after treatment. FINDINGS: Between Nov 15, 2019, and June 15, 2022, 210 participants (median age 35 years [IQR 27-44]) were enrolled. 135 (64%) participants were male and 72 (34%) were HIV positive. The pretreatment diagnostic sensitivities of TB-MBLA and Xpert-Ultra were similar (both 99% [95% CI 95-100]) but the specificity was higher for TB-MBLA (90% [83-96]) than for Xpert-Ultra (78% [68-86]). Ten participants were Xpert-Ultra trace positive, eight (80%) of whom were negative by TB-MBLA and MGIT culture. Smear microscopy had lower diagnostic sensitivity (75% [65-83]) but higher specificity (98% [93-100]) than TB-MBLA and Xpert-Ultra. Among participants who were smear microscopy negative, the sensitivity of TB-MBLA was 96% (95 CI 80-100) and was 100% (95% CI 86-100) in those who were HIV positive. 129 (61%) participants were identified as tuberculosis positive by Xpert-Ultra and these individuals were enrolled in the treatment group and monitored for treatment response. According to TB-MBLA, 19 of these patients cleared bacillary load to zero by week 2 of treatment and remained negative throughout the 6-month treatment follow-up. Positivity for tuberculosis decreased with treatment as measured by all tests, but the rate was slower with Xpert-Ultra. Consequently, 31 (33%) of 95 participants were still Xpert-Ultra positive at the end of treatment but were clinically well and negative on TB-MBLA and culture at 6 months of treatment. Two patients were still Xpert-Ultra positive with a further 3 months of post-treatment follow-up. The rate of conversion to negative of the DNA-based Xpert-Ultra was 3·3-times slower than that of the rRNA-based TB-MBLA. Consequently for the same patient, it would take 13 weeks and 52 weeks to reach complete tuberculosis negativity by TB-MBLA and Xpert-Ultra, respectively. Participants who were positive on smear microscopy at 8 weeks, who received an extra month of intensive treatment, had a similar TB-MBLA-measured bacillary load at 8 weeks to those who were smear microscopy negative. INTERPRETATION: TB-MBLA has a similar performance to Xpert-Ultra for pretreatment diagnosis of tuberculosis, but is more accurate at detecting and characterising the response to treatment than Xpert-Ultra and standard-of-care smear microscopy. FUNDING: European and Developing Countries Clinical Trials Partnership, Makerere University Research and Innovation Fund, US National Institutes of Health. | |
dc.format.extent | 183250 | |
dc.language.iso | eng | |
dc.relation.ispartof | The Lancet Microbe | en |
dc.subject | RA0421 Public health. Hygiene. Preventive Medicine | en |
dc.subject | E-DAS | en |
dc.subject | SDG 3 - Good Health and Well-being | en |
dc.subject.lcc | RA0421 | en |
dc.title | Accuracy of the tuberculosis molecular bacterial load assay to diagnose and monitor response to anti-tuberculosis therapy : a longitudinal comparative study with standard-of-care smear microscopy, Xpert MTB/RIF Ultra, and culture in Uganda | en |
dc.type | Journal article | en |
dc.contributor.sponsor | European and Developing Countries | en |
dc.contributor.institution | University of St Andrews. School of Medicine | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. Sir James Mackenzie Institute for Early Diagnosis | en |
dc.contributor.institution | University of St Andrews. Centre for Biophotonics | en |
dc.contributor.institution | University of St Andrews. Biomedical Sciences Research Complex | en |
dc.contributor.institution | University of St Andrews. Infection and Global Health Division | en |
dc.contributor.institution | University of St Andrews. Global Health Implementation Group | en |
dc.identifier.doi | https://doi.org/10.1016/S2666-5247(23)00367-1 | |
dc.description.status | Peer reviewed | en |
dc.identifier.grantnumber | en |
This item appears in the following Collection(s)
Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.