Abstract

We applied a metabonomic strategy to identify host biomarkers in serum to diagnose paediatric tuberculosis (TB) disease. 112 symptomatic children with presumptive TB were recruited in The Gambia and classified as bacteriologically-confirmed TB, clinically diagnosed TB, or other diseases. Sera were analysed using 1H nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS). Multivariate data analysis was used to distinguish patients with TB from other diseases. Diagnostic accuracy was evaluated using Receiver Operating Characteristic (ROC) curves. Model performance was tested in a validation cohort of 36 children from the UK. Data acquired using 1H NMR demonstrated a sensitivity, specificity and Area Under the Curve (AUC) of 69% (95% confidence interval [CI], 56–73%), 83% (95% CI, 73–93%), and 0.78 respectively, and correctly classified 20% of the validation cohort from the UK. The most discriminatory MS data showed a sensitivity of 67% (95% CI, 60–71%), specificity of 86% (95% CI, 75–93%) and an AUC of 0.78, correctly classifying 83% of the validation cohort. Amongst children with presumptive TB, metabolic profiling of sera distinguished bacteriologically-confirmed and clinical TB from other diseases. This novel approach yielded a diagnostic performance for paediatric TB comparable to that of Xpert MTB/RIF and interferon gamma release assays.

Highlights

  • Diagnostic signature, both gene expression profiling and flow cytometric measurements currently remain far removed from a point-of-care test

  • We report the application of 1H Nuclear Magnetic Resonance (NMR) spectroscopy and untargeted Ultra-performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) based assays, to identify diagnostic biomarkers of TB disease amongst children with presumptive TB in The Gambia

  • The most discriminatory MS data showed a sensitivity of 67%, specificity of 85% and correctly classified 83% of the validation cohort

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Summary

Introduction

Diagnostic signature, both gene expression profiling and flow cytometric measurements currently remain far removed from a point-of-care test. Protein-based diagnostics could be easier to translate into a point-of-care test, paediatric data is sparse[18]. A recent systematic review of TB biomarker data published since 2010 in over 400 scientific papers shows the overall activity in the field but contained only 6% of data relating to studies in children[19]. We report the application of 1H Nuclear Magnetic Resonance (NMR) spectroscopy and untargeted Ultra-performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) based assays, to identify diagnostic biomarkers of TB disease amongst children with presumptive TB in The Gambia. Novel host biomarkers of paediatric TB were detected and specific metabolites identified, showing promising diagnostic potential on a readily available biofluid

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