Can nasal-NO be used to differentiate between primary and secondary ciliary dyskinesia?

C. Krantz, A. Malinovischi, A. Hollsing, K. Alving (Uppsala, Sweden)

Source: Annual Congress 2011 - Role of the biomarkers in airway diseases
Session: Role of the biomarkers in airway diseases
Session type: Poster Discussion
Number: 4782

Congress or journal article abstractE-poster

Abstract

Bakground: Nasal nitric oxide (n-NO) has been suggested as a screening test for primary ciliary dyskinesia (PCD) as patients with PCD have lower n-NO levels than healthy controls. Recent studies on n-NO in PCD and secondary ciliary dyskinesia (SCD) show an overlap between these two groups.
Aim: To investigate in a pilot study if n-NO can differentiate between patients with diagnosed PCD and SCD treated at our centre.
Methods: n-NO was measured in duplicate by aspiration at 5 ml/s with NIOX Mino in 21 patients with clinically diagnosed PCD (n=12) or SCD (n=9). The electron microscopy (EM) results on brush samples from the nose were available in all subjects.
Results: Reproducibility of n-NO was good in each patient. A group of patients (n=6) had clearly low n-NO (5-69ppb) compared with the rest (216-857ppb). In the group with low n-NO there were only patients with PCD while in the group with high n-NO there were both patients with SCD and PCD, including 2 with Kartagener‘s syndrome. Regarding EM findings, the only 3 subjects with no dyneinarms were in the low n-NO while 8 subjects without structural abnormalities had high n-NO values. The relatively large group with more atypical or inconclusive results was also heterogenous with regard to n-NO levels.
Conclusion: A low n-NO value had a good positive predictive value for PCD in our material, but some PCD patients had normal n-NO levels. As structural findings on EM and n-NO appear to dissociate in some subjects, we continue to investigate all PCD and SCD patients at our centre including even functional tests of ciliary clearance, to see if n-NO correlates more to the cilia function than structural abnormalities.


Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
C. Krantz, A. Malinovischi, A. Hollsing, K. Alving (Uppsala, Sweden). Can nasal-NO be used to differentiate between primary and secondary ciliary dyskinesia?. Eur Respir J 2011; 38: Suppl. 55, 4782

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

Nilsson Harriet - 28.11.2011 11:39
Very nice poster and intersting data! Harriet
You must Login to comment this presentation.


Related content which might interest you:
Primary ciliary dyskinesia: the patients grow up
Source: Eur Respir J 2016; 48: 297-300
Year: 2016


Primary ciliary dyskinesia
Source: Breathe 2014; 10:122-133
Year: 2014




Primary ciliary dyskinesia
Source: International Congress 2018 – State of the art session: Paediatric respiratory diseases
Year: 2018


Transition in primary ciliary dyskinesia
Source: International Congress 2017 – PG16 Transition of children and adolescents into adult care
Year: 2017


Differentiation of primary and secondary ciliary dyskinesia with the quantitative analysis of ciliary elements
Source: Eur Respir J 2001; 18: Suppl. 33, 191s
Year: 2001

Is primary ciliary dyskinesia a "biofilm" disease?
Source: Annual Congress 2012 - New insights into respiratory infections in children
Year: 2012


Hypofertility in adult patients with primary ciliary dyskinesia
Source: International Congress 2017 – Paediatric bronchology in clinical practice
Year: 2017

Vestibular function in adult patients with primary ciliary dyskinesia
Source: Virtual Congress 2021 – Bronchiectasis and pleural infection
Year: 2021


Comparison of diagnostic tools for primary ciliary dyskinesia
Source: Annual Congress 2005 - New insights in respiratory infections in children
Year: 2005


Primary ciliary dyskinesia
Source: Eur Respir Mon 2011; 54: 201-217
Year: 2011


Primary ciliary dyskinesia: early diagnosis and impact on lung function
Source: Eur Respir J 2006; 28: Suppl. 50, 495s
Year: 2006

Primary ciliary dyskinesia in the neonatal period
Source: Eur Respir Monogr 2021; 92: 118-132
Year: 2021


Living with primary ciliary dyskinesia
Source: Breathe 2014; 10:157-159
Year: 2014


A process of years: coming to terms with primary ciliary dyskinesia
Source: Breathe, 16 (2) 200116; 10.1183/20734735.0116-2020
Year: 2020



Pulmonary care of primary ciliary dyskinesia (PCD)
Source: Eur Respir J 2005; 26: Suppl. 49, 628s
Year: 2005

Complete ciliary aplasia; a rare form of primary ciliary dyskinesia
Source: Eur Respir J 2005; 26: Suppl. 49, 302s
Year: 2005

The effect of L-arginine on ciliary function in primary ciliary dyskinesia (PCD)
Source: Annual Congress 2011 - Airways disease comorbidities and general aspects
Year: 2011

Problems of making and confirming the diagnosis of primary ciliary dyskinesia (PCD) in children still exist
Source: Annual Congress 2010 - Bronchoscopy and rare diseases in children
Year: 2010