Sputum and plasma adiponectin levels in clinically stable adult cystic fibrosis patients with CFTR I1234V mutation

A. Abdul Wahab (Doha, Qatar), M. Allangawi (Doha, Qatar), M. Thomas (Doha, Qatar), I. Bettahi (Doha, Qatar), S. Silvaraman (Doha, Qatar), J. Kumar (Doha, Qatar), P. Chandra (Doha, Qatar), M. Ramanjaneya (Doha, Qatar)

Source: International Congress 2018 – Cystic fibrosis in adults: current research
Session: Cystic fibrosis in adults: current research
Session type: Thematic Poster
Number: 1334

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:
A. Abdul Wahab (Doha, Qatar), M. Allangawi (Doha, Qatar), M. Thomas (Doha, Qatar), I. Bettahi (Doha, Qatar), S. Silvaraman (Doha, Qatar), J. Kumar (Doha, Qatar), P. Chandra (Doha, Qatar), M. Ramanjaneya (Doha, Qatar). Sputum and plasma adiponectin levels in clinically stable adult cystic fibrosis patients with CFTR I1234V mutation. 1334

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:
CFTR gene mutations detected in Japanese individuals with cystic fibrosis
Source: Eur Respir J 2006; 28: Suppl. 50, 716s
Year: 2006

KL-6 serum levels in adult cystic fibrosis patients
Source: Annual Congress 2011 - Cystic fibrosis: clinical and laboratory studies
Year: 2011

A novel CFTR mutation found in a Chinese cystic fibrosis patient
Source: Eur Respir J 2005; 26: Suppl. 49, 402s
Year: 2005

High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and ΔF508
Source: Eur Respir J 2001; 17: 1181-1186
Year: 2001



Analysis of CFTR gene mutations in 24 Japanese individuals with cystic fibrosis
Source: Annual Congress 2010 - Cystic fibrosis: lung disease infection and more
Year: 2010


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

Distinctive CFTR gene mutations found in Japanese individuals with cystic fibrosis
Source: Annual Congress 2004 - Cystic fibrosis in the 21st century: cutting edge investigations, taxing problems
Year: 2004


Genotype/phenotype correlation of the G85E mutation in a large cohort of cystic fibrosis patients
Source: Eur Respir J 2004; 23: 679-684
Year: 2004



Sputum glucose as a marker of disease severity in adult patients with cystic fibrosis
Source: International Congress 2018 – Cystic fibrosis in adults: current research
Year: 2018


Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two F508del alleles
Source: ERJ Open Res, 5 (2) 00082-2019; 10.1183/23120541.00082-2019
Year: 2019



Serum microRNA levels in paediatric females versus males with cystic fibrosis
Source: International Congress 2016 – What's new in biomarker analysis?
Year: 2016

Potentiating and correcting mutant CFTR in patients with cystic fibrosis
Source: Eur Respir Monogr 2014; 64: 129-149
Year: 2014


Nasal potential difference of carriers of the W493R ENaC variant with non-cystic fibrosis bronchiectasis
Source: Eur Respir J 2016; 47: 322-324
Year: 2016


Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the ΔF508 mutation
Source: Annual Congress 2003 - Cystic fibrosis: new genes, new controversies
Year: 2003


Sputum induction in young cystic fibrosis patients
Source: Eur Respir J 2001; 17: 832
Year: 2001


Morbidity and mortality in carriers of the cystic fibrosis mutation CFTR Phe508del in the general population
Source: Eur Respir J, 56 (3) 2000558; 10.1183/13993003.00558-2020
Year: 2020



Increased EMMPRIN and MT1-MMP levels in the plasma of the stable adult patients with cystic fibrosis
Source: Eur Respir J 2005; 26: Suppl. 49, 404s
Year: 2005

Genotypic diversity of Pseudomonas aeruginosa in cystic fibrosis patients with the CFTR I1234V mutation in a large kindred family
Source: Annual Congress 2012 - Cystic fibrosis (adults and children): risk factors and clinical problems
Year: 2012


Ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation
Source: Eur Respir Rev 2013; 22: 66-71
Year: 2013