Author:
AbdulWahab Atqah,Allangawi Mona,Thomas Merlin,Bettahi Ilham,Sivaraman Siveen K.,Jerobin Jayakumar,Chandra Prem,Abou-Samra Abdul-Badi,Ramanjaneya Manjunath
Abstract
Abstract
Background
Cystic fibrosis (CF) lung disease is associated with chronic inflammation leading to progress in lung function. Adiponectin is a predominantly anti-inflammatory adipokine that may have a role in CF lung. This study aims to determine total sputum and total plasma adiponectin levels in clinically stable adults CF patients with CFTR I1234V mutation, compared to plasma adiponectin levels in healthy controls and to investigate their correlations with body mass index (BMI) and spirometry in patients with CF.
Methods
A cross-sectional study comprises 17 CF patients and 18 healthy controls. Adiponectin levels were measured by magnetic bead-based multiplex assay.
Results
The mean age of adult CF patients was 22.9 years±3.8 (18–30) and 76.5% CF patients had pancreatic sufficiency. The mean BMI in healthy controls was slightly higher than CF patients. The mean sputum adiponectin level was significantly lower than plasma adiponectin levels in CF patients and healthy controls (p < 0.001), whereas no significant difference in plasma adiponectin levels between CF patients and healthy controls. The mean sputum adiponectin level was observed to be higher in CF patients with pancreatic insufficiency. Sputum adiponectin level was correlated positively with plasma adiponectin level in CF patients (r = 0.47, p = 0.06). Sputum and plasma adiponectin levels in CF patients were correlated negatively with BMI and percentage predicted forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC).
Conclusions
Sputum adiponectin may provide a minimally invasive tool in the assessment of inflammatory status in CF patients. A further larger study to address any difference in sputum and plasma adiponectin levels among CF patients with pancreatic sufficiency versus pancreatic insufficiency.
Publisher
Springer Science and Business Media LLC
Reference32 articles.
1. O'Sullivan BP, Flume P. The clinical approach to lung disease in patients with cystic fibrosis. SeminRespirCrit Care Med. 2009;30:505–13.
2. WHO. Genomic Resource Centre. Genes and Human Disease. Available from: http://www.who.int/genomics/public/genetic diseases/en/index2.html.
3. Abdul Wahab A, Al Thani G, Dawod ST, Kambouris M, Al Hamed M. Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V). J Trop Pediatr .2001;47:110–112.
4. Banjar, H., et al., Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia. Ann Trop Paediatr .1999; 19:69–73.
5. Abdel Rahman H, Abdul Wahab A, Al Rahman MO, Mostafa OA. Faecal elastase −1 concentration in cystic fibrosis patients with CFTR I1234V mutation. Acta Paediatr .2006; 95:1066–1069.
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