Plasma ceramides and sphingomyelins increase in primary ciliary dyskinesia but decrease in cystic fibrosis

D. Bal Topcu (Ankara, Turkey), G. Tugcu (Ankara, Turkey), F. Ozcan (Antalya, Turkey), M. Aslan (Antalya, Turkey), S. Esref (Ankara, Turkey), M. Gharibzadeh Hizal (Ankara, Turkey), E. Elmas Yalcin (Ankara, Turkey), D. Dogru Ersoz (Ankara, Turkey), U. Ozcelik (Ankara, Turkey), N. Kiper (Ankara, Turkey), I. Lay (Ankara, Turkey), Y. Oztas (Ankara, Turkey)

Source: International Congress 2018 – Latest developments in cystic fibrosis
Session: Latest developments in cystic fibrosis
Session type: Poster Discussion
Number: 3424
Disease area: Airway diseases, Paediatric lung diseases

Congress or journal article abstractE-poster

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
D. Bal Topcu (Ankara, Turkey), G. Tugcu (Ankara, Turkey), F. Ozcan (Antalya, Turkey), M. Aslan (Antalya, Turkey), S. Esref (Ankara, Turkey), M. Gharibzadeh Hizal (Ankara, Turkey), E. Elmas Yalcin (Ankara, Turkey), D. Dogru Ersoz (Ankara, Turkey), U. Ozcelik (Ankara, Turkey), N. Kiper (Ankara, Turkey), I. Lay (Ankara, Turkey), Y. Oztas (Ankara, Turkey). Plasma ceramides and sphingomyelins increase in primary ciliary dyskinesia but decrease in cystic fibrosis. 3424

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

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Elevated glucose concentrations in respiratory droplets of cystic fibrosis patients
Source: Eur Respir J 2002; 20: Suppl. 38, 527s
Year: 2002

Evidence for ciliary dyskinesia in cystic fibrosis
Source: Virtual Congress 2021 – Cystic fibrosis in children: various aspects
Year: 2021


Serum lipid concentrations and malnutrition in adult cystic fibrosis patients
Source: Eur Respir J 2006; 28: Suppl. 50, 58s
Year: 2006

Changes in airway inflammation during pulmonary exacerbations in patients with cystic fibrosis and primary ciliary dyskinesia
Source: Eur Respir J 2016; 47: 829-836
Year: 2016



Plasma fatty acids and lipid hydroperoxides increase after antibiotic therapy in cystic fibrosis
Source: Eur Respir J 2007; 29: 958-964
Year: 2007



Primary ciliary dyskinesia and mild cystic fibrosis: lung structure and function similarities.
Source: International Congress 2017 – Paediatric bronchology in clinical practice
Year: 2017

Comparison of patient care pathway between primary ciliary dyskinesia and cystic fibrosis
Source: Virtual Congress 2020 – From the bronchoscope to the clinic: paediatric bronchology at a glance
Year: 2020


Cough detection in cystic fibrosis, primary ciliary dyskinesia and health
Source: International Congress 2016 – Non-inflammatory assessment of airway disorders
Year: 2016

Short-chain fatty acids affect cystic fibrosis airway inflammation and bacterial growth
Source: Eur Respir J 2015; 46: 1033-1045
Year: 2015



The role of free fatty acids in idiopathic pulmonary fibrosis
Source: International Congress 2017 – From idiopathic pulmonary fibrosis (IPF) to rare diseases
Year: 2017



Primary ciliary dyskinesia and non Cystic fibrosis bronchiectasis
Source: ERS Skills Course 2016
Year: 2016

Comparison of bronchodilator responsiveness in children with primary ciliary dyskinesia and cystic fibrosis
Source: International Congress 2016 – Cystic fibrosis: inflammation, microbiology, management and monitoring
Year: 2016


Ventilation inhomogeneity in children with cystic fibrosis and primary ciliary dyskinesia
Source: Annual Congress 2012 - New developments in paediatric respiratory physiology
Year: 2012


Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function
Source: Eur Respir J 2014; 44: 1253-1261
Year: 2014



Functional dead space in children with cystic fibrosis or primary ciliary dyskinesia.
Source: International Congress 2018 – Assessing pathophysiology in children
Year: 2018

Aging decreases reversibility of pulmonary fibrosis by regulating PRDM16-related fatty acid metabolism in lung fibroblasts
Source: Virtual Congress 2021 – Translational and other aspects of idiopathic interstitial pneumonia
Year: 2021

The polyamine spermine is increased in cystic fibrosis airway secretions
Source: Annual Congress 2011 - Cystic fibrosis: New aspects of diagnosis, inflammation and detecting exacerbation
Year: 2011


Plasma levels of circulating cell-free DNA are increased in idiopathic pulmonary fibrosis but do not correlate with disease severity
Source: International Congress 2019 – Biomarkers of idiopathic interstitial pneumonia
Year: 2019

Differences in airway inflammation between children with primary ciliary dyskinesia (PCD) and cystic fibrosis (CF)
Source: International Congress 2014 – Cystic fibrosis: genotypes, inflammation and microbiology
Year: 2014

Bacterial biofilms in bronchiectasis of primary ciliary dyskinesia (PCD) in comparison with cystic fibrosis (CF)
Source: Annual Congress 2012 - Prognostic indices in respiratory infections
Year: 2012