Evidence map›Paper›PMID 39609478›Full record

ArticleScientific reports2024

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

Isabelle Öhrnberg, Lovisa Karlsson, Shumaila Sayyab, Jakob Paues, David Martínez-Enguita, Mika Gustafsson, Patricia Espinoza-Lopez, Melissa Méndez-Aranda, Ericka Meza, Cesar Ugarte-Gil and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Future Prospects for Using Clinical Phenotypes in Tuberculosis Precision Medicine-An Approach for Clinical Management.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Isabelle Öhrnberg *Division of Inflammation and Infection, Lab 1, Floor 12, Linköping University, 58185, Linköping, Sweden.
Lovisa Karlsson *Division of Inflammation and Infection, Lab 1, Floor 12, Linköping University, 58185, Linköping, Sweden.
Shumaila SayyabDivision of Inflammation and Infection, Lab 1, Floor 12, Linköping University, 58185, Linköping, Sweden.
Jakob PauesDivision of Inflammation and Infection, Lab 1, Floor 12, Linköping University, 58185, Linköping, Sweden.
David Martínez-EnguitaDepartment of Physics, Chemistry and Biology, Linköping University, Linköping, Sweden.
Mika GustafssonDepartment of Physics, Chemistry and Biology, Linköping University, Linköping, Sweden.
Patricia Espinoza-LopezFacultad de Medicina, Universidad Peruana Cayetano Heredia, Lima, Peru.
Melissa Méndez-ArandaLaboratorios de Investigación y Desarrollo, Facultad de Ciencias e Ingeniería, Universidad Peruana Cayetano Heredia, Lima, Peru.
Ericka MezaInstituto de Medicina Tropical Alexander Von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru.
Cesar Ugarte-GilFacultad de Medicina, Universidad Peruana Cayetano Heredia, Lima, Peru.
Nicholas KiprotichBiochemistry and Clinical Chemistry, Moi University, Eldoret, Kenya.
Lameck DieroAMPATH Kenya, Moi University, Eldoret, Kenya.
Ronald Tonui *AMPATH Kenya, Moi University, Eldoret, Kenya.
Maria Lerm *Division of Inflammation and Infection, Lab 1, Floor 12, Linköping University, 58185, Linköping, Sweden. maria.lerm@liu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

Indexed as

DNA MethylationMouth MucosaAdultAntitubercular AgentsFemaleHumansMachine LearningMaleMiddle AgedPilot ProjectsTuberculosisTuberculosis, PulmonaryAntitubercular AgentsBiosignaturesBuccal mucosaDNA methylationOral swabsTreatment monitoringTuberculosis

Identifiers

PMID39609478
PMCPMC11604703

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.