Volume 8 Supplement 1

3rd WAO International Scientific Conference (WISC) 2014

Open Access

YKL-40 correlates with the phenotype of asthma

  • Krzysztof Specjalski1 and
  • Ewa Jassem1
World Allergy Organization Journal20158(Suppl 1):A34

https://doi.org/10.1186/1939-4551-8-S1-A34

Published: 8 April 2015

Background

YKL-40 is a chitinase-like protein synthesized by human macrophages, monocytes, and neutrophils. Although it is not specific, YKL-40 has been shown to correlate with asthma, its severity and level of control. As asthma is heterogeneous, it would be useful to determine whether the marker’s levels correlate with phenotypes of the disease. The aim of the study was to investigate the relevance of YKL-40 as a biomarker of asthma phenotype.

Methods

Level of YKL-40 was determined by means of immunoassay in sera of 167 asthmatics (116 women, 51 men; aged 18-88; mean age: 49 years) and 81 healthy controls (50 women, 31 men; aged 18-86; mean age: 48 years). On the basis of clinical criteria asthmatics were divided into four groups: atopic – 83 patients, non-atopic - 63, aspirin asthma - 12, asthma with underlying vasculitis- 9. Differences between groups were compared with the use of U-Mann-Whitney’s test. Correlations between variables were assessed with Pearson’s test.

Results

YKL-40 levels were significantly higher, on average, in asthmatics compared to control group (mean levels: 66,8 U/l and 44,9 U/l respectively; p<0,001). YKL-40 correlated with lack of asthma control (p<0,001) and diagnosis of exacerbation (p<0,001). The highest mean concentration was found in atopic asthmatics – 72U/l which was significantly higher compared to non-atopic patients – 61 U/l (p<0,05). Weak correlations were found between YKL-40 levels and CRP as well as FEV1. However no correlations have been found between YKL-40 level and sex, blood eosinophils count and neutrophils count.

Conclusions

YKL-40 correlates with asthma control, atopy, FEV1 and CRP. The latter suggests that YKL-40 concentration may depend on severity of inflammation what seems confirmed by the elevated levels in numerous inflammatory diseases and neoplasms.

Authors’ Affiliations

(1)
Medical University of Gdansk

Copyright

© Specjalski and Jassem; licensee BioMed Central Ltd. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement