The TB27 Transcriptomic Model for Predicting Mycobacterium tuberculosis Culture Conversion.
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BORIS DOI
Date of Publication
2024
Publication Type
Article
Division/Institute
Contributor
Reimann, Maja | |
Avsar, Korkut | |
DiNardo, Andrew R | |
Goldmann, Torsten | |
Hoelscher, Michael | |
Ibraim, Elmira | |
Kalsdorf, Barbara | |
Kaufmann, Stefan H E | |
Köhler, Niklas | |
Mandalakas, Anna M | |
Maurer, Florian P | |
Müller, Marius | |
Nitschkowski, Dörte | |
Olaru, Ioana D | |
Popa, Cristina | |
Rachow, Andrea | |
Rolling, Thierry | |
Salzer, Helmut J F | |
Sanchez-Carballo, Patricia | |
Schuhmann, Maren | |
Schaub, Dagmar | |
Spinu, Victor | |
Terhalle, Elena | |
Unnewehr, Markus | |
Zielinski, Nika J | |
Heyckendorf, Jan | |
Lange, Christoph |
Subject(s)
Series
Pathogens and Immunity
ISSN or ISBN (if monograph)
2469-2964
Publisher
Case Western Reserve University
Language
English
Publisher DOI
PubMed ID
39911144
Uncontrolled Keywords
Description
Rationale
Treatment monitoring of tuberculosis patients is complicated by a slow growth rate of Mycobacterium tuberculosis. Recently, host RNA signatures have been used to monitor the response to tuberculosis treatment.Objective
Identifying and validating a whole blood-based RNA signature model to predict microbiological treatment responses in patients on tuberculosis therapy.Methods
Using a multi-step machine learning algorithm to identify an RNA-based algorithm to predict the remaining time to culture conversion at flexible time points during anti-tuberculosis therapy.Results
The identification cohort included 149 patients split into a training and a test cohort, to develop a multistep algorithm consisting of 27 genes (TB27) for predicting the remaining time to culture conversion (TCC) at any given time. In the test dataset, predicted TCC and observed TCC achieved a correlation coefficient of r=0.98. An external validation cohort of 34 patients shows a correlation between predicted and observed days to TCC also of r=0.98.Conclusion
We identified and validated a whole blood-based RNA signature (TB27) that demonstrates an excellent agreement between predicted and observed times to M. tuberculosis culture conversion during tuberculosis therapy. TB27 is a potential useful biomarker for anti-tuberculosis drug development and for prediction of treatment responses in clinical practice.
Treatment monitoring of tuberculosis patients is complicated by a slow growth rate of Mycobacterium tuberculosis. Recently, host RNA signatures have been used to monitor the response to tuberculosis treatment.Objective
Identifying and validating a whole blood-based RNA signature model to predict microbiological treatment responses in patients on tuberculosis therapy.Methods
Using a multi-step machine learning algorithm to identify an RNA-based algorithm to predict the remaining time to culture conversion at flexible time points during anti-tuberculosis therapy.Results
The identification cohort included 149 patients split into a training and a test cohort, to develop a multistep algorithm consisting of 27 genes (TB27) for predicting the remaining time to culture conversion (TCC) at any given time. In the test dataset, predicted TCC and observed TCC achieved a correlation coefficient of r=0.98. An external validation cohort of 34 patients shows a correlation between predicted and observed days to TCC also of r=0.98.Conclusion
We identified and validated a whole blood-based RNA signature (TB27) that demonstrates an excellent agreement between predicted and observed times to M. tuberculosis culture conversion during tuberculosis therapy. TB27 is a potential useful biomarker for anti-tuberculosis drug development and for prediction of treatment responses in clinical practice.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| 770-Reimann12925b.pdf | text | Adobe PDF | 2.26 MB | Attribution (CC BY 4.0) | published |