Literature DB >> 17238189

The relationship of clinical and inflammatory markers to outcome in stable patients with cystic fibrosis.

Damian G Downey1, S Lorraine Martin, Martin Dempster, John E Moore, Mary T Keogan, Barry Starcher, Julia Edgar, Diana Bilton, J Stuart Elborn.   

Abstract

Decreased survival in patients with cystic fibrosis has been related to FEV1, BMI, and infection with Burkholderia cepacia complex (BCC). We have assessed the relationship of blood, sputum, and urine inflammatory markers to lung function, BMI, colonization with B cenocepacia (Bc), and patient survival. Thirty-nine stable cystic fibrosis (CF) patients (10 with Bc) were enrolled in a study to determine the effect of alpha-1-antitrypsin on airways inflammation. Pre-treatment measurements were used in this study. Demographics, sputum microbiology, heart rate, oxygen saturation, lung function were recorded. Blood samples were obtained for white blood count (WBC), C-Reactive Protein (CRP), and plasma neutrophil elastase/AAT complexes (pNEC). Neutrophil elastase (NE), neutrophil elastase/AAT complexes (sNEC), interleukin-8 (IL-8), TNF-receptor 1 (sTNFr), and myeloperoxidase (MPO) were measured in sputum and urinary desmosine concentration determined. Patients with Bc had significantly higher levels of pNEC, 332 +/- 91.4 ng/ml (mean +/- SEM) versus 106 +/- 18.2 ng/ml (P = 0.0005) and sNEC, 369 +/- 76.6 ng/ml versus 197 +/- 36.0 ng/ml compared to those who were not. Five deaths were reported at the end of 1 year, (four with Bc) (P = 0.011). Patients who subsequently died had significantly lower lung function FEV1, 1.2 +/- 0.2 L versus 2.0 +/- 0.1 L (P = 0.03) and FVC, 2 +/- 0.3 L versus 3.1 +/- 0.2 L (P = 0.01), compared to those that survived. There was significantly higher NE activity, 3.6 +/- 1.6 U/ml versus 1.5 +/- 0.6 U/ml (P = 0.03), pNEC, 274 +/- 99 ng/ml versus 142 +/- 30 ng/ml (P = 0.05), MPO, 163 +/- 62 mcg/ml versus 54 +/- 6.9 mcg/ml (P = 0.03), and urinary desmosines 108 +/- 19.9 pM/mg creatinine versus 51.1 +/- 3.3 pM/mg creatinine (P = 0.001), in those patients who subsequently died compared to those that survived. These data suggest there is increased neutrophil degranulation in patients infected with Bc and these patients have a poor outcome. 2007 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17238189     DOI: 10.1002/ppul.20553

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  20 in total

Review 1.  Proteases, cystic fibrosis and the epithelial sodium channel (ENaC).

Authors:  P H Thibodeau; M B Butterworth
Journal:  Cell Tissue Res       Date:  2012-05-22       Impact factor: 5.249

2.  Sputum desmosine during hospital admission for pulmonary exacerbation in cystic fibrosis.

Authors:  Theresa A Laguna; Brandie D Wagner; Heidi K Luckey; Shelley A Mann; Scott D Sagel; Warren Regelmann; Frank J Accurso
Journal:  Chest       Date:  2009-06-30       Impact factor: 9.410

3.  Urinary desmosine: a biomarker of structural lung injury during CF pulmonary exacerbation.

Authors:  Theresa A Laguna; Brandie D Wagner; Barry Starcher; Heidi K Luckey Tarro; Shelley A Mann; Scott D Sagel; Frank J Accurso
Journal:  Pediatr Pulmonol       Date:  2012-03-19

4.  Neutrophils as a Potential Source of Chitinase-3-like Protein 1 in Cystic Fibrosis.

Authors:  Adèle Coriati; Chantal Massé; Aurélie Ménard; Guillaume F Bouvet; Yves Berthiaume
Journal:  Inflammation       Date:  2018-10       Impact factor: 4.092

5.  The applicability of urinary creatinine as a method of specimen normalization in the cystic fibrosis population.

Authors:  Brandie D Wagner; Frank J Accurso; Theresa A Laguna
Journal:  J Cyst Fibros       Date:  2010-03-15       Impact factor: 5.482

Review 6.  Sputum biomarkers of inflammation in cystic fibrosis lung disease.

Authors:  Scott D Sagel; James F Chmiel; Michael W Konstan
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

Review 7.  Highlights of a workshop to discuss targeting inflammation in cystic fibrosis.

Authors:  Katharine H Banner; Hugo De Jonge; Stuart Elborn; Ellena Growcott; Erich Gulbins; Mike Konstan; Rick Moss; Chris Poll; Scott H Randell; Adriano G Rossi; Lorraine Thomas; David Waltz
Journal:  J Cyst Fibros       Date:  2008-11-20       Impact factor: 5.482

Review 8.  Using bacterial biomarkers to identify early indicators of cystic fibrosis pulmonary exacerbation onset.

Authors:  Geraint B Rogers; Lucas R Hoffman; Matt W Johnson; Nicole Mayer-Hamblett; Jürgen Schwarze; Mary P Carroll; Kenneth D Bruce
Journal:  Expert Rev Mol Diagn       Date:  2011-03       Impact factor: 5.225

9.  Burkholderia cenocepacia type VI secretion system mediates escape of type II secreted proteins into the cytoplasm of infected macrophages.

Authors:  Roberto Rosales-Reyes; Daniel F Aubert; Jennifer S Tolman; Amal O Amer; Miguel A Valvano
Journal:  PLoS One       Date:  2012-07-25       Impact factor: 3.240

10.  Evaluation of airway and circulating inflammatory biomarkers for cystic fibrosis drug development.

Authors:  Raksha Jain; Arthur Baines; Umer Khan; Brandie D Wagner; Scott D Sagel
Journal:  J Cyst Fibros       Date:  2020-07-01       Impact factor: 5.482

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.