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Plasma YKL-40 and all-cause mortality in patients with chronic obstructive pulmonary disease Holmgaard DB; Mygind LH; Titlestad IL; Madsen H; Pedersen SS; Johansen JS; Pedersen CBMC Pulm Med 2013[Dec]; 13 (ä): 77BACKGROUND: Chronic obstructive pulmonary disease (COPD) is hallmarked by inflammatory processes and a progressive decline of lung function. YKL-40 is a potential biomarker of inflammation and mortality in patients suffering from inflammatory lung disease, but its prognostic value in patients with COPD remains unknown. We investigated whether high plasma YKL-40 was associated with increased mortality in patients with moderate to very severe COPD. METHODS: Four hundred and ninety-three patients with moderate to very severe COPD were followed prospectively for up to 10 years. Patients were divided into two groups according to plasma YKL-40: concentration higher than the 75th percentile for age-matched healthy subjects (i.e. high levels) and normal levels. Outcome was overall survival (OS) and was evaluated in uni- and multivariate proportional hazards Cox regression analyses and adjusted for factors affecting mortality. RESULTS: Median plasma YKL-40 was increased in patients with COPD (81 ng/ml, p < 0.001) compared to healthy subjects (40 ng/ml). Patients with high plasma YKL-40 had a hazard ratio (HR) of 1.42 (95% CI: 1.15-1.75, p = 0.001) for all-cause mortality. Multivariate analysis showed that YKL-40 (HR 1.38; 95% CI: 1.11-1.72, p = 0.004), age (HR 1.05; 95% CI: 1.03-1.06, p < 0.0001), Severe COPD (HR 1.35; 95 CI: 1.03-1.76, p = 0.03) very severe COPD (HR 2.19; 95% CI: 1.60 - 2.99 < 0.0001), neutrophil granulocyte count (HR 1.05; 95% CI: 1.01-1.08, p = 0.01), and a smoking history of > 40 years (HR 1.38; 95% CI: 1.11-1.71, p = 0.003) were independent prognostic markers of OS. CONCLUSION: High plasmaYKL-40 is associated with increased mortality in patients with moderate to very severe COPD, suggesting a role for YKL-40 as a potential biomarker of mortality in this patient group.|Adipokines/*blood[MESH]|Age Factors[MESH]|Aged[MESH]|Biomarkers/blood[MESH]|Case-Control Studies[MESH]|Chitinase-3-Like Protein 1[MESH]|Female[MESH]|Granulocytes[MESH]|Humans[MESH]|Lectins/*blood[MESH]|Leukocyte Count[MESH]|Longitudinal Studies[MESH]|Male[MESH]|Neutrophils[MESH]|Proportional Hazards Models[MESH]|Pulmonary Disease, Chronic Obstructive/*blood/*mortality[MESH]|Severity of Illness Index[MESH]|Smoking/mortality[MESH] |
