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


Autoria(s): Downey, Damian; Martin, Lorraine; Dempster, Martin; Moore, John E.; Keogan, M.T.; Starcher, B.; Edgar, J.; Bilton, D.; Elborn, Joseph
Data(s)

01/03/2007

Resumo

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.

Identificador

http://pure.qub.ac.uk/portal/en/publications/the-relationship-of-clinical-and-inflammatory-markers-to-outcome-in-stable-patients-with-cystic-fibrosis(44a9259d-b5a3-4b52-b5bb-54cc71e90346).html

http://dx.doi.org/10.1002/ppul.20553

http://www.scopus.com/inward/record.url?scp=33947263039&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/closedAccess

Fonte

Downey , D , Martin , L , Dempster , M , Moore , J E , Keogan , M T , Starcher , B , Edgar , J , Bilton , D & Elborn , J 2007 , ' The relationship of clinical and inflammatory markers to outcome in stable patients with cystic fibrosis ' Pediatric Pulmonology , vol 42 , no. 3 , pp. 216-220 . DOI: 10.1002/ppul.20553

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700/2735 #Pediatrics, Perinatology, and Child Health #/dk/atira/pure/subjectarea/asjc/2700/2740 #Pulmonary and Respiratory Medicine
Tipo

article