%0 Journal Article
%T The relationship of systemic inflammation to prior hospitalization in adult patients with cystic fibrosis
%A David A Ngan
%A Pearce G Wilcox
%A May Aldaabil
%A Yuexin Li
%A Jonathon A Leipsic
%A Don D Sin
%A SF Man
%J BMC Pulmonary Medicine
%D 2012
%I BioMed Central
%R 10.1186/1471-2466-12-3
%X This cross-sectional study included 58 consecutive, clinically stable adults from the CF Clinic at St. Paul's Hospital (Vancouver, Canada). Blood levels of interleukin (IL)-6, IL-1¦Â, C-reactive protein (CRP), interleukin (IL)-6, IL-1¦Â, granzyme B (GzmB), chemokine C-C motif ligand 18 (CCL18/PARC), surfactant protein D (SP-D), lipopolysaccharide (LPS)-binding protein, and soluble cluster of differentiation 14 (sCD14) were measured using enzyme-linked immunosorbent assays, and LPS levels were measured using a Limulus amebocyte lysate assay. Spirometry was also performed. Multivariable linear regression analysis was used to assess relationships of the blood biomarkers to lung function.Lung function impairment was independently associated with elevated plasma levels of CRP (P < 0.01), IL-6 (P = 0.04), IL-1¦Â (P < 0.01), and LBP (P < 0.01). Increasing age (P < 0.01), reduced body mass index (P = 0.02), prior hospitalizations (P = 0.03), and presence of Pseudomonas aeruginosa in sputum cultures (P < 0.01) were also associated with reduced lung function. Elevated concentrations of LPS in plasma were associated with a previous history of hospitalization (P < 0.05). There was a trend towards an increase in plasma IL-6 (P = 0.07) and IL-1¦Â (P = 0.06) levels in patients who were previously hospitalized.IL-6 and IL-1¦Â are promising systemic biomarkers for lung function impairment and history of hospitalization in adult patients with CF.Cystic fibrosis (CF) is a progressive, debilitating disease that affects nearly 30,000 Americans and occurs with a frequency of about 1 in 3500 births [1]. It is characterized by persistent lung infection and lung function impairment. It also affects other organs including the sinuses, gastrointestinal tract, endocrine glands, and the bone [2-5]. Although all CF cases are caused by a mutation in the gene for the CF transmembrane conductance regulator, there is considerable heterogeneity in the rate at which the disease progresses [6]. The traditio
%U http://www.biomedcentral.com/1471-2466/12/3