Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/9422
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dc.contributor.authorÖhrnberg, Isabelle-
dc.contributor.authorKarlsson, Lovisa-
dc.contributor.authorSayyab, Shumaila-
dc.contributor.authorPaues, Jakob-
dc.contributor.authorMartínez-Enguita, David-
dc.contributor.authorGustafsson, Mika-
dc.contributor.authorEspinoza-Lopez, Patricia-
dc.contributor.authorKiprotich, Nicholas-
dc.contributor.authorDiero, Lameck-
dc.contributor.authorTonui, Ronald-
dc.contributor.authorLerm, Maria-
dc.date.accessioned2024-12-02T07:54:09Z-
dc.date.available2024-12-02T07:54:09Z-
dc.date.issued2024-11-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/9422-
dc.description.abstractTuberculosis (TB) poses a significant global health threat, with high mortality rates if left untreated. Current sputum-based TB treatment monitoring methods face numerous challenges, particularly in relation to sample collection and analysis. This pilot study explores the potential of TB status assessment using DNA methylation (DNAm) signatures, which are gaining recognition as diagnostic and predictive tools for various diseases. We collected buccal swab samples from pulmonary TB patients at the commencement of TB treatment (n=10), and at one, two, and six-month follow-up intervals. We also collected samples from healthy controls (n=10) and individuals exposed to TB (n=10). DNAm patterns were mapped using the Illumina Infinium Methylation EPIC 850 K platform. A DNAm profile distinct from controls was discovered in the oral mucosa of TB patients at the start of treatment, and this profile changed throughout the course of TB treatment. These findings were corroborated in a separate validation cohort of TB patients (n=41), monitored at two and six months into their TB treatment. We developed a machine learning model to predict symptom scores using the identified DNAm TB profile. The model was trained and evaluated on the pilot, validation, and two additional independent cohorts, achieving an R2 of 0.80, Pearson correlation of 0.90, and mean absolute error of 0.13. While validation is needed in larger cohorts, the result opens the possibility of employing DNAm-based diagnostic and prognostic tools for TB in future clinical practice.en_US
dc.language.isoenen_US
dc.publishernatureportfolioen_US
dc.subjectTuberculosisen_US
dc.subjectBiosignaturesen_US
dc.titleA DNA methylation signature identified in the buccal mucosa reflecting active tuberculosis is changing during tuberculosis treatmenten_US
dc.typeArticleen_US
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