Evidence map›Paper›PMID 23737604›Full record

ArticleThe Journal of infectious diseases2013

Impaired pulmonary nitric oxide bioavailability in pulmonary tuberculosis: association with disease severity and delayed mycobacterial clearance with treatment.

Anna P Ralph, Tsin W Yeo, Cheryl M Salome, Govert Waramori, Gysje J Pontororing, Enny Kenangalem, Sandjaja, Emiliana Tjitra, Richard Lumb, Graeme P Maguire and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Can lipid body-positive rates ofFrontiers in immunology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Metabolic Regulation of Immune Responses toFrontiers in immunology · 2020
    Review
  14. Article
  15. Exhaled Nitric Oxide is Not a Biomarker for Pulmonary Tuberculosis.The American journal of tropical medicine and hygiene · 2018
    Article
  16. Review
  17. Review
  18. Article
  19. Arginine adjunctive therapy in active tuberculosis.Tuberculosis research and treatment · 2015
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 8 institutions in 3 countries.

Anna P RalphGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory 0810, Australia. anna.ralph@menzies.edu.au
Tsin W Yeo
Cheryl M Salome
Govert Waramori
Gysje J Pontororing
Enny Kenangalem
Sandjaja
Emiliana Tjitra
Richard Lumb
Graeme P Maguire
Ric N Price
Mark D Chatfield
Paul M Kelly
Nicholas M Anstey
Menzies School of Health Research · AUCharles Darwin University · AUMinistry of Health · IDRoyal Darwin Hospital · AUAustralian National University · AUJames Cook University · AUSouth Australia Pathology · AUWoolcock Institute of Medical Research · AU

Funding

Wellcome Trust 091625
6 · The paper itself

Abstract

backgroundNitric oxide (NO), a key macrophage antimycobacterial mediator that ameliorates immunopathology, is measurable in exhaled breath in individuals with pulmonary tuberculosis. We investigated relationships between fractional exhale NO (FENO) and initial pulmonary tuberculosis severity, change during treatment, and relationship with conversion of sputum culture to negative at 2 months.

methodsIn Papua, we measured FENO in patients with pulmonary tuberculosis at baseline and serially over 6 months and once in healthy controls. Treatment outcomes were conversion of sputum culture results at 2 months and time to conversion of sputum microscopy results.

resultsAmong 200 patients with pulmonary tuberculosis and 88 controls, FENO was lower for patients with pulmonary tuberculosis at diagnosis (geometric mean FENO, 12.7 parts per billion [ppb]; 95% confidence interval [CI], 11.6-13.8) than for controls (geometric mean FENO, 16.6 ppb; 95% CI, 14.2-19.5; P = .002), fell further after treatment initiation (nadir at 1 week), and then recovered by 6 months (P = .03). Lower FENO was associated with more-severe tuberculosis disease, with FENO directly proportional to weight (P < .001) and forced vital-capacity (P = .001) and inversely proportional to radiological score (P = .03). People whose FENO increased or remained unchanged by 2 months were 2.7-fold more likely to achieve conversion of sputum culture than those whose FENO decreased (odds ratio, 2.72; 95% CI, 1.05-7.12; P = .04).

conclusionsAmong patients with pulmonary tuberculosis, impaired pulmonary NO bioavailability is associated with more-severe disease and delayed mycobacterial clearance. Measures to increase pulmonary NO warrant investigation as adjunctive tuberculosis treatments.

Indexed as

Severity of Illness IndexAdolescentAdultAgedAntitubercular AgentsBacterial LoadBiological AvailabilityBody WeightBreath TestsFemaleHumansLungMaleMiddle AgedNitric OxideRadiographyAntitubercular AgentsNitric Oxidebiomarkerexhaled nitric oxideL-arginineM2 macrophagestuberculosis

Identifiers

PMID23737604
PMCPMC3719909
OpenAlexW2245573514

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.