Exhaled nitric oxide is not a biomarker for pulmonary tuberculosis
- ,
- Maria Cristina I. Loader(corresponding author),
- Daniel Smith,
- Daniel Pastorius,
- Marjory Bravard,
- Luz Caviedes
- ,
- Instituto Nacional de Salud del Niño San Borja,
- Universidad Peruana Cayetano Heredia,
- Asociación Benéfica PRISMA,
- Imperial College London,
- Massachusetts General Hospital
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Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 1637-1639 (3 pages)Journal (Volume, Issue Number)
American Journal of Tropical Medicine and Hygiene (Volume 98, Issue 6)Publication milestones
- Published - 2018
Publication status
ISSN
0002-9637Publication IDs
- Scopus: 85048249921
- PubMed: 29714162
Abstract
To reduce transmission of tuberculosis (TB) in resource-limited countries where TB remains a major cause of mortality, novel diagnostic tools are urgently needed. We evaluated the fractional concentration of exhaled nitric oxide (FeNO) as an easily measured, noninvasive potential biomarker for diagnosis and monitoring of treatment response in participants with pulmonary TB including multidrug resistant–TB in Lima, Peru. In a longitudinal study however, we found no differences in baseline median FeNO levels between 38 TB participants and 93 age-matched controls (13 parts per billion [ppb] [interquartile range (IQR) = 8–26] versus 15 ppb [IQR = 12–24]), and there was no change over 60 days of treatment (15 ppb [IQR = 10–19] at day 60). Taking this and previous evidence together, we conclude FeNO is not of value in either the diagnosis of pulmonary TB or as a marker of treatment response.
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