Combining blood transcriptomic signatures improves the prediction of progression to tuberculosis among household contacts in Brazil

Combining blood transcriptomic signatures improves the prediction of progression to tuberculosis among household contacts in Brazil

Publication date: Sep 20, 2025

Tuberculosis remains a major health threat, infecting nearly a third of the world’s population. Of those infected, 5-10% progress from latent infection to active tuberculosis (TB) disease and biomarkers to identify which individuals will progress are needed to allow targeted prophylactic treatment. Several risk biomarkers have been developed to predict progression but have not been tested head-to-head on the same platform. Here, we used the NanoString platform and compared the performance of 15 published gene signatures in predicting progression at baseline in a household contact cohort. Expression of gene signatures was profiled in RNA extracted from whole blood and scored using GSVA and PLAGE. We found that specificity is enhanced by combining signatures and report that the performance of a combined signature that includes a newly derived parsimonious signature through machine learning and a published signature met WHO TPP levels for a triage test. The combined signature had a 90.9% sensitivity and 88% specificity with a PPV of 0.24 and NPV of 1. This combined signature has potential clinical utility in identifying high-risk individuals for targeted prophylaxis to prevent TB morbidity and mortality.

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Concepts Keywords
Biotechnol Certified
Housekeeping False
Tuberculosis Gsva
Viral Medrxiv
Peer
Plage
Ppv
Preprint
Progression
Progressors
Sensitivity
Signature
Signatures
Specificity
Table

Semantics

Type Source Name
disease IDO blood
disease MESH tuberculosis
pathway KEGG Tuberculosis
disease MESH latent infection
drug DRUGBANK Methionine
disease MESH morbidity
disease MESH infection
disease IDO host
disease MESH viral infections
disease IDO assay
pathway REACTOME Digestion
drug DRUGBANK Water
disease IDO process
disease MESH confusion
disease IDO algorithm
drug DRUGBANK Flunarizine
disease IDO cell
disease IDO intervention
disease MESH respiratory infections
disease MESH re infection
drug DRUGBANK Isoniazid
disease IDO bacteria
disease MESH Allergy
disease MESH Infectious Diseases
disease MESH pulmonary tuberculosis

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