Literature DB >> 23742758

Combined Cathepsin S and hs-CRP predicting inflammation of abdominal aortic aneurysm.

Yanwen Qin1, Yaoguo Yang2, Rong Liu2, Xu Cao2, Ou Liu2, Jing Liu2, Miao Wang2, Ya Yang2, Zhong Chen2, Hongjia Zhang2, Jie Du2.   

Abstract

OBJECTIVES: Cathepsin S (Cat S) protein expression is increased in human abdominal aortic aneurysm (AAA) lesions and Cat S has been suggested a direct role by promoting inflammatory response partly in experimental AAA. The purpose of this study is to observe the expression of serum Cat S and hs-CRP and its clinical significance in AAA patients. DESIGN AND METHODS: We collected serum samples from 31 AAA patients and 32 controls. Cat S and hs-CRP levels were measured by a sandwich-type enzyme-linked immunosorbent assay (ELISA) and an enhanced immunoturbidimetric assay respectively. The maximum diameter of the AAA was identified by ultrasonography.
RESULTS: The patients with AAA had higher serum Cat S and hs-CRP levels than the controls (p<0.05). Furthermore, human serum Cat S levels were strongly correlated with hs-CRP by the nonparametric Spearman correlation tests (B=0.849, p<0.05). Based on Pearson's correlation test, human serum Cat S and hs-CRP levels were positively correlated with AAA diameter size (p<0.05). Cat S was correlated independently with the hs-CRP in all subjects (p<0.01). After adjustment for the maximum diameter of the abdominal aorta-associated variables, Cat S combined hs-CRP (R(2)=0.801) is better than Cat S (R(2)=0.740) in predicting the maximum diameter of AAA lesions.
CONCLUSION: Combined serum Cat S and hs-CRP levels are better in predicting the inflammatory activity of AAA lesions in the clinical setting.
Copyright © 2013 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abdominal aortic aneurysm; Cathepsin S; High-sensitivity CRP; Inflammation

Mesh:

Substances:

Year:  2013        PMID: 23742758     DOI: 10.1016/j.clinbiochem.2013.05.065

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


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