Urinary drug metabolite profiling of tuberculosis treatment failure using proton nuclear magnetic resonance.

J Pharm Biomed Anal

Human Metabolomics, North-West University (Potchefstroom Campus), Private Bag x6001, Box 269, Potchefstroom 2531, South Africa. Electronic address:

Published: September 2024

AI Article Synopsis

  • - The study investigates the unknown reasons behind treatment failure in tuberculosis (TB) by using a specialized H NMR technique to analyze TB drug levels and their metabolites in the urine of patients.
  • - Urine samples were taken from patients at different stages of TB treatment and analyzed to compare drug concentrations between those who were cured and those who experienced treatment failure.
  • - Results indicated that metabolites of isoniazid (INH) were higher in patients who did not respond effectively to treatment, suggesting that factors beyond genetics, like environmental influences and variations in metabolic pathways, may play a significant role in treatment failure.

Article Abstract

The underlying cause of tuberculosis (TB) treatment failure is still largely unknown. A H NMR approach was applied to identify and quantify a subset of TB drugs and drug metabolites: ethambutol (EMB), acetyl isoniazid (AcINH), isonicotinic acid, pyrazinamide (PZA), pyrazinoic acid and 5-hydroxy-pyrazinoic acid, from the urine of TB patients. Samples were collected before, during (weeks one, two and four) and after standardised TB treatment. The median concentrations of the EMB and PZA metabolites were comparable between the samples from patients with eventually cured and failed treatment outcomes. The INH metabolites showed comparatively elevated concentrations in the treatment failure patients during and after treatment. Variation in INH metabolite concentrations couldn't be associated with the varying acetylator genotypes, and it is therefore suggested that treatment failure is influenced more so by other conditions, such as environmental factors, or individual variation in other INH metabolic pathways.

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Source
http://dx.doi.org/10.1016/j.jpba.2024.116297DOI Listing

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