Evidence map›Paper›PMID 24024753›Full record

ArticleAnnals of the American Thoracic Society2013

Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.

Margaret W Leigh, Milan J Hazucha, Kunal K Chawla, Brock R Baker, Adam J Shapiro, David E Brown, Lisa M Lavange, Bethany J Horton, Bahjat Qaqish, Johnny L Carson and 12 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Annals of the American Thoracic Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00807482 (Diagnostic and Clinical Characterization of Patients With Unusual Genetic Disorders of the Airways), which is not on this map. Cited by 140 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 8 pooled it
17.5field-weighted citation impact, top 1% 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.

NCT00807482 recruitingnot on this map

Diagnostic and Clinical Characterization of Patients With Unusual Genetic Disorders of the Airways

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2004 to 2027Enrolled1,800ConditionsKartagener Syndrome
3 · Its place in the literature

Who cites it

140 citing papers in PubMed, 8 syntheses or guidelines pooled it, 264 citations in OpenAlex.

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  17. A Case of Primary Ciliary Dyskinesia Caused byCase reports in medicine · 2026
    Article
  18. Article
  19. Article
  20. Primary ciliary dyskinesia.Paediatrics & child health · 2025
    Article

80 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 11 institutions in 2 countries.

Margaret W Leigh1 Department of Pediatrics.
Milan J Hazucha
Kunal K Chawla
Brock R Baker
Adam J Shapiro
David E Brown
Lisa M Lavange
Bethany J Horton
Bahjat Qaqish
Johnny L Carson
Stephanie D Davis
Sharon D Dell
Thomas W Ferkol
Jeffrey J Atkinson
Kenneth N Olivier
Scott D Sagel
Margaret Rosenfeld
Carlos Milla
Hye-Seung Lee
Jeffrey Krischer
Maimoona A Zariwala
Michael R Knowles
University of North Carolina at Chapel Hill · USUniversity of South Florida · USWashington University in St. Louis · USIndiana University · USInstitute for Clinical Evaluative Sciences · CANational Institute of Allergy and Infectious Diseases · USPediatrics and Genetics · USSeattle Children's Hospital · USStanford University · USUniversity of Colorado Denver · USUniversity of South Carolina · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Biostatstics for Research in Environmental HealthT32ES007018 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel, Rebecca Fry · 1985 to 2026
$31.3M
Colorado Clinical and Translational Science Institute (UL1)UL1TR000154 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2012 to 2013
$20.4M
Pathogenesis of PCD Lung DiseaseR01HL071798 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNOWLES, MICHAEL R · 2004 to 2021
$7.2M
GENETIC DISORDERS OF MUCOCILIARY CLEARANCE: RARE DISEASES: PCD, CF, &PHA U54RR019480 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNOWLES, MICHAEL R · 2004 to 2008
$6.0M
Intramural NIH HHSNCATS NIH HHS UL1 TR000154NCATS NIH HHS UL1TR000154NCATS NIH HHS UL1 TR001082NCRR NIH HHS U54 RR019480NHLBI NIH HHS 5R01HL071798NHLBI NIH HHS NIH 5 U54 HL09640958-09NHLBI NIH HHS R01 HL071798NIEHS NIH HHS NIH T32ES007018NIEHS NIH HHS T32 ES007018PHS HHS CTSA NIH/NCATS UNC ULTR000083
6 · The paper itself

Abstract

rationaleSeveral studies suggest that nasal nitric oxide (nNO) measurement could be a test for primary ciliary dyskinesia (PCD), but the procedure and interpretation have not been standardized.

objectivesTo use a standard protocol for measuring nNO to establish a disease-specific cutoff value at one site, and then validate at six other sites.

methodsAt the lead site, nNO was prospectively measured in individuals later confirmed to have PCD by ciliary ultrastructural defects (n = 143) or DNAH11 mutations (n = 6); and in 78 healthy and 146 disease control subjects, including individuals with asthma (n = 37), cystic fibrosis (n = 77), and chronic obstructive pulmonary disease (n = 32). A disease-specific cutoff value was determined, using generalized estimating equations (GEEs). Six other sites prospectively measured nNO in 155 consecutive individuals enrolled for evaluation for possible PCD. MEASUREMENTS AND MAIN

resultsAt the lead site, nNO values in PCD (mean ± standard deviation, 20.7 ± 24.1 nl/min; range, 1.5-207.3 nl/min) only rarely overlapped with the nNO values of healthy control subjects (304.6 ± 118.8; 125.5-867.0 nl/min), asthma (267.8 ± 103.2; 125.0-589.7 nl/min), or chronic obstructive pulmonary disease (223.7 ± 87.1; 109.7-449.1 nl/min); however, there was overlap with cystic fibrosis (134.0 ± 73.5; 15.6-386.1 nl/min). The disease-specific nNO cutoff value was defined at 77 nl/minute (sensitivity, 0.98; specificity, >0.999). At six other sites, this cutoff identified 70 of the 71 (98.6%) participants with confirmed PCD.

conclusionsUsing a standardized protocol in multicenter studies, nNO measurement accurately identifies individuals with PCD, and supports its usefulness as a test to support the clinical diagnosis of PCD.

Indexed as

AdolescentAdultAgedAsthmaAxonemal DyneinsBreath TestsCase-Control StudiesChildChild, PreschoolCiliaCystic FibrosisFemaleHumansKartagener SyndromeMaleMicroscopy, Electron, TransmissionAxonemal DyneinsDNAH11 protein, humanNitric Oxide

Identifiers

PMID24024753
PMCPMC3960971
OpenAlexW1965779264

What OpenQuestion holds

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Registered trials

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.