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Levels of YKL-40 in pleural effusions and blood from patients with pulmonary or pleural disease

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Abstract
Background: YKL-40 (a chitinase-like protein) is an inflammatory biomarker that is associated with lung injury pathogenesis. We aimed to identify the diagnostic values of YKL-40 in pleural effusions and to evaluate circulating YKL-40 levels during multiple etiological pulmonary/pleural diseases and the role of YKL-40 as a monitoring marker of inflammatory pulmonary disease. Methods: Pleural YKL-40 (n = 197), YKL-39 (the most homologous chitinase-like protein to human YKL-40), and conventional pleural marker levels were measured in patients with pulmonary/pleural disease. Additionally, serum YKL-40 and YKL-39 levels were analyzed in both patients and controls (n = 432) and serially monitored in patients with asthma (n = 27) or pneumonia (n = 22). Results: Pleural YKL-40 levels were higher than those in the serum and highest in tuberculous pleural effusions (TPEs: 1181 ng/mL), followed by parapneumonic, malignant, and cardiogenic effusions (560 ng/mL). The diagnostic accuracy of pleural YKL-40 (0.78) for discriminating between tuberculous and malignant effusion was comparable to or greater than those of YKL-39, total protein, C-reactive protein and CYFRA 21-1, and lower than those of adenosine deaminase (p < 0.05) and carcinoembriogenic antigen (p = 0.05). Serum YKL-40 levels were higher in the pneumonia group than in the cancer, asthma, or control groups. Following treatment, serum YKL-40 levels were more greatly reduced in pneumonia patients than in asthma patients. Serum YKL-39 levels did not differ between patients and controls. Conclusions: Pleural YKL-40 levels are elevated in TPEs and have fairly good diagnostic efficacy for detecting TPEs. However, adenosine deaminase is more efficient for detecting TPEs than pleural YKL-40. Serum YKL-40 levels are highest during pneumonia compared to common pulmonary/pleural diseases and are more useful for monitoring pneumonia than asthma. (C) 2012 Elsevier Ltd. All rights reserved.
Author(s)
Kim, Hak-RyulJun, Chang-DukLee, Koung-SunCho, Ji-HyunJeong, Eun-TaikYang, Sei-HoonLee, Young-JinPark, Do-Sim
Issued Date
2012-06
Type
Article
DOI
10.1016/j.cyto.2012.03.001
URI
https://scholar.gist.ac.kr/handle/local/15938
Publisher
Academic Press
Citation
Cytokine, v.58, no.3, pp.336 - 343
ISSN
1043-4666
Appears in Collections:
Department of Life Sciences > 1. Journal Articles
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