The diagnostic potential of urine in paediatric patients undergoing initial treatment for tuberculous meningitis
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Abstract
Tuberculous meningitis (TBM)--the extrapulmonary form of tuberculosis, is the most severe
complication associated with tuberculosis, particularly in infants and children. The gold standard for
the diagnosis of TBM requires cerebrospinal fluid (CSF) through lumbar puncture--an invasive sample
collection method, and currently available CSF assays are often not sufficient for a definitive TBM
diagnosis. Urine is metabolite-rich and relatively unexplored in terms of its potential to diagnose
neuroinfectious diseases. We used an untargeted proton magnetic resonance (1
H-NMR) metabolomics
approach to compare the urine from 32 patients with TBM (stratified into stages 1, 2 and 3) against
that from 39 controls in a South African paediatric cohort. Significant spectral bins had to satisfy three
of our four strict cut-off quantitative statistical criteria. Five significant biological metabolites were
identified--1-methylnicotinamide, 3-hydroxyisovaleric acid, 5-aminolevulinic acid, N-acetylglutamine
and methanol--which had no correlation with medication metabolites. ROC analysis revealed that
methanol lacked diagnostic sensitivity, but the other four metabolites showed good diagnostic
potential. Furthermore, we compared mild (stage 1) TBM and severe (stages 2 and 3) TBM, and our
multivariate metabolic model could successfully classify severe but not mild TBM. Our results show
that urine can potentially be used to diagnose severe TBM.
