Literature DB >> 24024753

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

Margaret W Leigh1, 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.   

Abstract

RATIONALE: Several 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.
OBJECTIVES: To use a standard protocol for measuring nNO to establish a disease-specific cutoff value at one site, and then validate at six other sites.
METHODS: At 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 RESULTS: At 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.
CONCLUSIONS: Using 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.

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Year:  2013        PMID: 24024753      PMCID: PMC3960971          DOI: 10.1513/AnnalsATS.201305-110OC

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  33 in total

1.  Diagnostic value of nasal nitric oxide measured with non-velum closure techniques for children with primary ciliary dyskinesia.

Authors:  Dimas Mateos-Corral; Robin Coombs; Hartmut Grasemann; Felix Ratjen; Sharon D Dell
Journal:  J Pediatr       Date:  2011-04-22       Impact factor: 4.406

Review 2.  Primary ciliary dyskinesia: improving the diagnostic approach.

Authors:  Margaret W Leigh; Maimoona A Zariwala; Michael R Knowles
Journal:  Curr Opin Pediatr       Date:  2009-06       Impact factor: 2.856

3.  Primary ciliary dyskinesia in Amish communities.

Authors:  Hauw Lie; Maimoona A Zariwala; Cynthia Helms; Anne M Bowcock; John L Carson; David E Brown; Milan J Hazucha; James Forsen; David Molter; Michael R Knowles; Margaret W Leigh; Thomas W Ferkol
Journal:  J Pediatr       Date:  2010-03-29       Impact factor: 4.406

4.  Inner dynein arm defects causing primary ciliary dyskinesia: repeat testing required.

Authors:  C O'Callaghan; A Rutman; G M Williams; R A Hirst
Journal:  Eur Respir J       Date:  2011-03-15       Impact factor: 16.671

5.  Nitric oxide and the paranasal sinuses.

Authors:  Jon O Lundberg
Journal:  Anat Rec (Hoboken)       Date:  2008-11       Impact factor: 2.064

6.  Early lung disease in young children with primary ciliary dyskinesia.

Authors:  David E Brown; Jessica E Pittman; Margaret W Leigh; Lynn Fordham; Stephanie D Davis
Journal:  Pediatr Pulmonol       Date:  2008-05

7.  Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects.

Authors:  Niki Tomas Loges; Heike Olbrich; Anita Becker-Heck; Karsten Häffner; Angelina Heer; Christina Reinhard; Miriam Schmidts; Andreas Kispert; Maimoona A Zariwala; Margaret W Leigh; Michael R Knowles; Hanswalter Zentgraf; Horst Seithe; Gudrun Nürnberg; Peter Nürnberg; Richard Reinhardt; Heymut Omran
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

8.  Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children.

Authors:  A Barbato; T Frischer; C E Kuehni; D Snijders; I Azevedo; G Baktai; L Bartoloni; E Eber; A Escribano; E Haarman; B Hesselmar; C Hogg; M Jorissen; J Lucas; K G Nielsen; C O'Callaghan; H Omran; P Pohunek; M-P F Strippoli; A Bush
Journal:  Eur Respir J       Date:  2009-12       Impact factor: 16.671

9.  Nasal nitric oxide assessment in primary ciliary dyskinesia using aspiration, exhalation, and humming.

Authors:  Francesca Santamaria; Sara De Stefano; Silvia Montella; Federico Barbarano; Paola Iacotucci; Roberto Ciccarelli; Matteo Sofia; Mauro Maniscalco
Journal:  Med Sci Monit       Date:  2008-02

10.  Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing.

Authors:  Jonathan S Berg; James P Evans; Margaret W Leigh; Heymut Omran; Chris Bizon; Ketan Mane; Michael R Knowles; Karen E Weck; Maimoona A Zariwala
Journal:  Genet Med       Date:  2011-03       Impact factor: 8.822

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  90 in total

Review 1.  Genetics and biology of primary ciliary dyskinesia.

Authors:  Amjad Horani; Thomas W Ferkol; Susan K Dutcher; Steven L Brody
Journal:  Paediatr Respir Rev       Date:  2015-09-11       Impact factor: 2.726

2.  Nasal nitric oxide is an important test in the diagnostic pathway for primary ciliary dyskinesia.

Authors:  Jane S Lucas; Woolf T Walker
Journal:  Ann Am Thorac Soc       Date:  2013-12

3.  Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p.

Authors:  Adam J Shapiro; Karen E Weck; Kay C Chao; Margaret Rosenfeld; Anders O H Nygren; Michael R Knowles; Margaret W Leigh; Maimoona A Zariwala
Journal:  J Pediatr       Date:  2014-07-25       Impact factor: 4.406

4.  Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype.

Authors:  Stephanie D Davis; Thomas W Ferkol; Margaret Rosenfeld; Hye-Seung Lee; Sharon D Dell; Scott D Sagel; Carlos Milla; Maimoona A Zariwala; Jessica E Pittman; Adam J Shapiro; Johnny L Carson; Jeffrey P Krischer; Milan J Hazucha; Matthew L Cooper; Michael R Knowles; Margaret W Leigh
Journal:  Am J Respir Crit Care Med       Date:  2015-02-01       Impact factor: 21.405

5.  Summary for Clinicians: Diagnosis of Primary Ciliary Dyskinesia.

Authors:  Michael G O'Connor; Anne Griffiths; Narayan P Iyer; Adam J Shapiro; Kevin C Wilson; Carey C Thomson
Journal:  Ann Am Thorac Soc       Date:  2019-02

6.  C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.

Authors:  Mahmoud R Fassad; Amelia Shoemark; Pierrick le Borgne; France Koll; Mitali Patel; Mellisa Dixon; Jane Hayward; Charlotte Richardson; Emily Frost; Lucy Jenkins; Thomas Cullup; Eddie M K Chung; Michel Lemullois; Anne Aubusson-Fleury; Claire Hogg; David R Mitchell; Anne-Marie Tassin; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

7.  Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.

Authors:  Adam J Shapiro; Stephanie D Davis; Deepika Polineni; Michele Manion; Margaret Rosenfeld; Sharon D Dell; Mark A Chilvers; Thomas W Ferkol; Maimoona A Zariwala; Scott D Sagel; Maureen Josephson; Lucy Morgan; Ozge Yilmaz; Kenneth N Olivier; Carlos Milla; Jessica E Pittman; M Leigh Anne Daniels; Marcus Herbert Jones; Ibrahim A Janahi; Stephanie M Ware; Sam J Daniel; Matthew L Cooper; Lawrence M Nogee; Billy Anton; Tori Eastvold; Lynn Ehrne; Elena Guadagno; Michael R Knowles; Margaret W Leigh; Valery Lavergne
Journal:  Am J Respir Crit Care Med       Date:  2018-06-15       Impact factor: 21.405

8.  Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia.

Authors:  Timothy J Vece; Scott D Sagel; Maimoona A Zariwala; Kelli M Sullivan; Kimberlie A Burns; Susan K Dutcher; Roman Yusupov; Margaret W Leigh; Michael R Knowles
Journal:  Pediatr Pulmonol       Date:  2019-09-23

9.  Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

Authors:  Adam J Shapiro; Stephanie D Davis; Thomas Ferkol; Sharon D Dell; Margaret Rosenfeld; Kenneth N Olivier; Scott D Sagel; Carlos Milla; Maimoona A Zariwala; Whitney Wolf; Johnny L Carson; Milan J Hazucha; Kimberlie Burns; Blair Robinson; Michael R Knowles; Margaret W Leigh
Journal:  Chest       Date:  2014-11       Impact factor: 9.410

Review 10.  Primary Ciliary Dyskinesia: An Update on New Diagnostic Modalities and Review of the Literature.

Authors:  Rizwana Popatia; Kenan Haver; Alicia Casey
Journal:  Pediatr Allergy Immunol Pulmonol       Date:  2014-06-01       Impact factor: 1.349

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