Monomeric calgranulins measured by SELDI-TOF mass spectrometry and calprotectin measured by ELISA as biomarkers in arthritis

被引:72
作者
de Seny, Dominique [1 ]
Fillet, Marianne [2 ]
Ribbens, Clio
Maree, Raphaeel [3 ]
Meuwis, Marie-Alice [2 ]
Lutteri, Laurence [2 ]
Chapelle, Jean-Paul [2 ]
Wehenkel, Louis [4 ]
Louis, Edouard [5 ]
Merville, Marie-Paule [2 ]
Malaise, Michel
机构
[1] Univ Liege, Tour GIGA, Lab Rheumatol, CHU,GIGA Res, B-4000 Liege, Belgium
[2] Univ Liege, Clin Chem Lab, GIGA Res, B-4000 Liege, Belgium
[3] Univ Liege, GIGA Bioinformat Platform, B-4000 Liege, Belgium
[4] Univ Liege, GIGA Res, Bioinformat & Modeling Unit, Dept Elect Engn & Comp Sci, B-4000 Liege, Belgium
[5] Univ Liege, CHU, Lab Hepatogastroenterol, B-4000 Liege, Belgium
关键词
D O I
10.1373/clinchem.2007.099549
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: SELDI-TOF mass spectrometry (MS) is a high-throughput proteomic approach with potential for identifying novel forms of serum biomarkers of arthritis. METHODS: We used SELDI-TOF MS to analyze serum samples from patients with various forms of inflammatory arthritis. Several protein profiles were collected on different Bio-Rad Laboratories ProteinChip arrays (CM 10 and IMAC-Cu2+) and were evaluated statistically to select potential biomarkers. RESULTS: SELDI-TOF MS analyses identified several calgranulin proteins [S100A8 (calgranulin A), S100A9 (calgranulin B), S100A9*, and S100A12 (calgranulin C)], serum amyloid A (SAA), SAA des-Arg (SAA-R), and SAA des-Arg/des-Ser (SAA-RS) as biomarkers and confirmed the results with other techniques, such as western blotting, immunoprecipitation, and nano-LCMS/MS. The S 100 proteins were all able to significantly differentiate samples from patients with rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS) from those of patients with inflammatory bowel diseases used as an inflammatory control (IC) group, whereas the SAA, SAA-R, and SAA-RS proteins were not, with the exception of AS. The 4 S100 proteins were coproduced in all of the pathologies and were significantly correlated with the plasma calprotectin concentration; however, these S100 proteins were correlated with the SAA peak intensities only in the RA and IC patient groups. In RA, these S 100 proteins (except for S100A12) were significantly correlated with the serum concentrations of C-reactive protein, matrix metalloproteinase 3, and anti-cyclic citrullinated peptide and with the Disease Activity Score (DAS(28)). CONCLUSIONS: The SELDI-TOF MS technology is a powerful approach for analyzing the status of monomeric, truncated, or posttranslationally modified forms of arthritis biomarkers, such as the S100A8, S100A9, S100A12, and SAA proteins. The fact that the SELDI-TOF MS data were correlated with results obtained with the classic calprotectin ELISA test supports the reliability of this new proteomic technique. (c) 2008 American Association for Clinical Chemistry.
引用
收藏
页码:1066 / 1075
页数:10
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