Literature DB >> 18187313

Nasal nitric oxide for early diagnosis of primary ciliary dyskinesia: practical issues in children.

Giorgio L Piacentini1, Alessandro Bodini, Diego Peroni, Erika Rigotti, Roberta Pigozzi, Ugo Pradal, Attilio L Boner.   

Abstract

BACKGROUND: Primary ciliary dyskinesia (PCD) is a genetic disease characterized by abnormally beating cilia. In these patients, levels of nasal nitric oxide (nNO) are lower than those observed in healthy subjects.
OBJECTIVES: We identify the nNO levels in healthy pre-school uncooperative children and in PCD patients, in order the application of nNO measurement in the early identification of young children with PCD.
METHODS: We measured nNO in 77 healthy children (50 uncooperative and 27 cooperative) and in 10 PCD patients. Fifteen cooperative healthy children were also asked to perform an uncooperative test.
RESULTS: PCD patients presented low nNO levels (29.7+/-5.7 ppb) compared to those observed in healthy children (358.8+/-35.2 ppb; p<0.05). nNO levels were increased in healthy cooperative children (650+/-60.6 ppb; p<0.05) as compared to those uncooperative aging more than 6 month (309.1+/-45.9 ppb; p<0.05) or less (128.1+/-16.2 ppb; p<0.05). Twenty-four uncooperative children with nNO values < or = 200 ppb performed a second evaluation at least 6 months later and mean levels increased from 104.7+/-10.5 ppb to 169.9+/-19.6 ppb (p<0.05). In the 15 collaborative children nNO levels were higher during the breath holding manoeuvre (687.7+/-96.9 ppb) than during the tidal breathing manoeuvre (335.9+/-57.9 ppb; p<0.05).
CONCLUSIONS: Healthy children have higher nNO levels than PCD patients. In 15% of uncooperative healthy children can be found low nNO levels, similar to PCD patients, but those values increased some months later, in successive evaluations. Nasal NO may be used for PCD screening even though repeated evaluations may be necessary in young children.

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Year:  2008        PMID: 18187313     DOI: 10.1016/j.rmed.2007.11.013

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  10 in total

Review 1.  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

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

Review 3.  Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia. A Systematic Review and Meta-analysis.

Authors:  Adam J Shapiro; Maureen Josephson; Margaret Rosenfeld; Ozge Yilmaz; Stephanie D Davis; Deepika Polineni; Elena Guadagno; Margaret W Leigh; Valery Lavergne
Journal:  Ann Am Thorac Soc       Date:  2017-07

Review 4.  Update of respiratory tract disease in children with primary ciliary dyskinesia.

Authors:  Scott D Sagel; Stephanie D Davis; Paolo Campisi; Sharon D Dell
Journal:  Proc Am Thorac Soc       Date:  2011-09

5.  Primary ciliary dyskinesia: evaluation using cilia beat frequency assessment via spectral analysis of digital microscopy images.

Authors:  Mary A K Olm; João E Kögler; Mariangela Macchione; Amelia Shoemark; Paulo H N Saldiva; Joaquim C Rodrigues
Journal:  J Appl Physiol (1985)       Date:  2011-05-05

6.  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

7.  The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia.

Authors:  Raymond H Kim; David A Hall; Ernest Cutz; Michael R Knowles; Kathleen A Nelligan; Keith Nykamp; Maimoona A Zariwala; Sharon D Dell
Journal:  Ann Am Thorac Soc       Date:  2014-03

Review 8.  Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.

Authors:  Margaret W Leigh; Jessica E Pittman; Johnny L Carson; Thomas W Ferkol; Sharon D Dell; Stephanie D Davis; Michael R Knowles; Maimoona A Zariwala
Journal:  Genet Med       Date:  2009-07       Impact factor: 8.822

9.  Clinical value of measurement of pulmonary radioaerosol mucociliary clearance in the work up of primary ciliary dyskinesia.

Authors:  Mathias Munkholm; Kim Gjerum Nielsen; Jann Mortensen
Journal:  EJNMMI Res       Date:  2015-07-16       Impact factor: 3.138

10.  Diagnostic accuracy of nasal nitric oxide for establishing diagnosis of primary ciliary dyskinesia: a meta-analysis.

Authors:  Panayiotis Kouis; Stefania I Papatheodorou; Panayiotis K Yiallouros
Journal:  BMC Pulm Med       Date:  2015-12-03       Impact factor: 3.317

  10 in total

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