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Exhaled nitric oxide is not a biomarker for pulmonary tuberculosis

  • ,
  • Maria Cristina I. Loader
    ,
  • 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
Research Output: Contribution to journal Article Peer-review

Open access

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages 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

Published - 2018

ISSN

0002-9637

Publication 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.

Funding Details

Financial support: This work was supported by the Gates Challenge Grant; the Fogarty Foundation Fellows program of Vanderbilt University (grant number R24 TW007988 to J. W. L.) and the University of North Carolina; and the National Institutes of Health. J. S. F. and MC. I. L. are grateful for financial support from the Imperial College Biomedical Research Centre. This work was supported by the Gates Challenge Grant; the Fogarty Foundation Fellows program of Vanderbilt University (grant number R24 TW007988 to J. W. L.) and the University of North Carolina; and the National Institutes of Health. J. S. F. and MC. I. L. are grateful for financial support from the Imperial College Biomedical Research Centre.
FundersFunding numbers
Fogarty Foundation
-
Fogarty Foundation Fellows program of
-
NIH
-
Vanderbilt University
R24 TW007988
UNC
-
MRC
MR/N001192/1
Imperial College London
-
BRC
-

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