A DNA methylation signature identified in the buccal mucosa reflecting active tuberculosis is changing during tuberculosis treatment.

Publication date: Nov 28, 2024

Tuberculosis (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 R 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.

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Concepts Keywords
Global Adult
Mucosa Antitubercular Agents
Pilot Antitubercular Agents
Prognostic Biosignatures
Tuberculosis Buccal mucosa
DNA Methylation
DNA methylation
Female
Humans
Machine Learning
Male
Middle Aged
Mouth Mucosa
Oral swabs
Pilot Projects
Treatment monitoring
Tuberculosis
Tuberculosis
Tuberculosis, Pulmonary

Semantics

Type Source Name
drug DRUGBANK Spinosad
drug DRUGBANK Coenzyme M
disease MESH Infection
disease MESH Inflammation
drug DRUGBANK Ethambutol
drug DRUGBANK Pyrazinamide
drug DRUGBANK Rifampicin
drug DRUGBANK Isoniazid
disease MESH COVID 19 pandemic
disease MESH death
disease MESH infectious diseases
disease IDO symptom
pathway REACTOME Methylation
pathway KEGG Tuberculosis
disease MESH tuberculosis
pathway REACTOME DNA methylation
disease MESH HIV infection
pathway REACTOME HIV Infection
disease IDO bacteria
disease MESH co infection
disease IDO blood
disease IDO algorithm
disease IDO assay
disease MESH Yersinia infection
pathway KEGG Yersinia infection
disease MESH Papillomavirus infection
disease MESH Shigellosis
pathway KEGG Shigellosis
disease MESH Salmonella infection
pathway KEGG Salmonella infection
disease IDO immunodeficiency
disease MESH virus infection
pathway KEGG Chemokine signaling pathway
disease IDO host
disease MESH abnormalities
drug DRUGBANK BCG vaccine
disease MESH scar
drug DRUGBANK Fenamole
disease MESH pulmonary tuberculosis
disease MESH extrapulmonary tuberculosis
pathway KEGG Glutamatergic synapse
pathway KEGG Hippo signaling pathway
disease IDO country
disease MESH dyspnea
disease MESH chest pain
disease IDO process
disease IDO site
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
pathway KEGG Neurotrophin signaling pathway
disease MESH lung diseases
disease MESH sarcoidosis
disease IDO immunosuppression
drug DRUGBANK Heparin
drug DRUGBANK Gold
drug DRUGBANK Phosphate ion
drug DRUGBANK Albendazole
disease IDO history
drug DRUGBANK (S)-Des-Me-Ampa
disease IDO cell
disease MESH asthma
pathway KEGG Asthma
disease MESH fibrosis
disease MESH lung cancer
disease MESH post acute COVID 19 syndrome
disease MESH latent tuberculosis infection
drug DRUGBANK Boron
disease MESH obesity
disease IDO susceptibility
disease MESH treatment failure
disease MESH comorbidity
drug DRUGBANK Ademetionine
pathway REACTOME Reproduction

Original Article

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