dc.contributor.author | Nordal, Hilde Haugedal | en_US |
dc.contributor.author | Brun, Johan Gorgas | en_US |
dc.contributor.author | Halse, Anne-Kristine | en_US |
dc.contributor.author | Jonsson, Roland | en_US |
dc.contributor.author | Fagerhol, Magne Kristoffer | en_US |
dc.contributor.author | Hammer, Hilde Berner | en_US |
dc.date.accessioned | 2014-10-13T13:39:25Z | |
dc.date.available | 2014-10-13T13:39:25Z | |
dc.date.issued | 2014-10-04 | eng |
dc.identifier.issn | 1471-2474 | |
dc.identifier.uri | https://hdl.handle.net/1956/8632 | |
dc.description.abstract | Background: The calcium-binding protein S100A12 correlates with measures of disease activity in patients with rheumatoid arthritis (RA). The protein reflects neutrophil activation and the present objective was to explore in a pilot study the associations between S100A12 and other inflammatory markers, clinical assessments as well as degree of synovitis detected by a comprehensive ultrasonography (US) examination in RA patients during biologic treatment. Methods: Twenty patients with RA were examined clinically and by use of US as well as laboratory markers S100A12, calprotectin, C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) before starting adalimumab, with follow-up after 1, 3, 6 and 12 months. Ultrasonographic B-mode (BM) and power Doppler (PD) assessments of 78 joints, 36 tendons/tendon groups and 2 bursas were performed, and sum US scores calculated. Wilcoxon signed rank test assessed treatment response and Spearman rank correlation test was used to calculate correlations. Results: The concentrations of S100A12 decreased after 3 months (p < 0.01) and significant correlations were found between S100A12 and the other laboratory markers during follow-up (0.50-0.62, p < 0.05). Of the clinical assessments, S100A12 had highest correlations with the assessor’s global VAS (0.46-0.85, p < 0.05). Compared with CRP and ESR, S100A12 showed higher correlations with the sum US scores (both BM and PD), with median (range) correlation coefficients of 0.55 (0.35-0.78 (NS-p < 0.001)) for sum BM scores and 0.45 (0.27-0.75 (NS-p < 0.001)) for sum PD scores. Conclusions: The S100A12 protein was significantly associated with other inflammatory markers, clinical assessments as well as sum US scores, indicating that S100A12 is a potential marker of inflammation in RA patients. | en_US |
dc.language.iso | eng | eng |
dc.publisher | BioMed Central | eng |
dc.rights | Attribution CC BY | eng |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0 | eng |
dc.subject | S100 proteins | eng |
dc.subject | S100A12 | eng |
dc.subject | Ultrasonography | eng |
dc.subject | Rheumatoid arthritis | eng |
dc.subject | Inflammation | eng |
dc.subject | Biologic therapy | eng |
dc.title | The neutrophil protein S100A12 is associated with a comprehensive ultrasonographic synovitis score in a longitudinal study of patients with rheumatoid arthritis treated with adalimumab | en_US |
dc.type | Peer reviewed | |
dc.type | Journal article | |
dc.date.updated | 2014-10-11T03:02:55Z | |
dc.description.version | publishedVersion | en_US |
dc.rights.holder | Copyright 2014 Nordal et al.; licensee BioMed Central Ltd. | |
dc.rights.holder | Hilde Haugedal Nordal et al.; licensee BioMed Central Ltd. | |
dc.source.articlenumber | 335 | |
dc.identifier.doi | https://doi.org/10.1186/1471-2474-15-335 | |
dc.identifier.cristin | 1162606 | |
dc.source.journal | BMC Musculoskeletal Disorders | |
dc.source.40 | 15 | |