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The neutrophil protein S100A12 is associated with a comprehensive ultrasonographic synovitis score in a longitudinal study of patients with rheumatoid arthritis treated with adalimumab

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 marker...

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Main Authors: Nordal, Hilde Haugedal, Brun, Johan G, Halse, Anne-Kristine, Jonsson, Roland, Fagerhol, Magne Kristoffer, Hammer, Hilde Berner
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Brun, Johan G
Halse, Anne-Kristine
Jonsson, Roland
Fagerhol, Magne Kristoffer
Hammer, Hilde Berner
description 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 
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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 &lt; 0.01) and significant correlations were found between S100A12 and the other laboratory markers during follow-up (0.50-0.62, p &lt; 0.05). Of the clinical assessments, S100A12 had highest correlations with the assessor’s global VAS (0.46-0.85, p &lt; 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 &lt; 0.001)) for sum BM scores and 0.45 (0.27-0.75 (NS-p &lt; 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.</description><language>eng</language><publisher>BioMed Central</publisher><subject>Biologic therapy ; Inflammation ; Rheumatoid arthritis ; S100 proteins ; S100A12 ; Ultrasonography</subject><creationdate>2014</creationdate><rights>info:eu-repo/semantics/openAccess</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,780,885,26565</link.rule.ids><linktorsrc>$$Uhttp://hdl.handle.net/1956/11796$$EView_record_in_NORA$$FView_record_in_$$GNORA$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Nordal, Hilde Haugedal</creatorcontrib><creatorcontrib>Brun, Johan G</creatorcontrib><creatorcontrib>Halse, Anne-Kristine</creatorcontrib><creatorcontrib>Jonsson, Roland</creatorcontrib><creatorcontrib>Fagerhol, Magne Kristoffer</creatorcontrib><creatorcontrib>Hammer, Hilde Berner</creatorcontrib><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</title><description>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 &lt; 0.01) and significant correlations were found between S100A12 and the other laboratory markers during follow-up (0.50-0.62, p &lt; 0.05). Of the clinical assessments, S100A12 had highest correlations with the assessor’s global VAS (0.46-0.85, p &lt; 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 &lt; 0.001)) for sum BM scores and 0.45 (0.27-0.75 (NS-p &lt; 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.</description><subject>Biologic therapy</subject><subject>Inflammation</subject><subject>Rheumatoid arthritis</subject><subject>S100 proteins</subject><subject>S100A12</subject><subject>Ultrasonography</subject><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNqFjTFOA0EMRbdJgYArIF8gUgZEUEoUgdKTfmVmnYylWXtle4NysxwvI6Cgo_q_eP_9m-6yLwRCc5hOhStMpkEs8JFWq9f0COyA7poZgwb44iiAkHWcjAqJ84lgrmHoKno0bI4MfhY9cbSpZzWCpkOoKkeOeWDBCt7KGfQAEwaThP-YrdA8YigPgBbFvh1h9Od7wMpjgz7vusUBq9P9b952D-9v--1umY09WHpRwz5tntd9Si-b9dO_wBVzoF2d</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Nordal, Hilde Haugedal</creator><creator>Brun, Johan G</creator><creator>Halse, Anne-Kristine</creator><creator>Jonsson, Roland</creator><creator>Fagerhol, Magne Kristoffer</creator><creator>Hammer, Hilde Berner</creator><general>BioMed Central</general><scope>3HK</scope></search><sort><creationdate>2014</creationdate><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</title><author>Nordal, Hilde Haugedal ; Brun, Johan G ; Halse, Anne-Kristine ; Jonsson, Roland ; Fagerhol, Magne Kristoffer ; Hammer, Hilde Berner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-cristin_nora_1956_117963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biologic therapy</topic><topic>Inflammation</topic><topic>Rheumatoid arthritis</topic><topic>S100 proteins</topic><topic>S100A12</topic><topic>Ultrasonography</topic><toplevel>online_resources</toplevel><creatorcontrib>Nordal, Hilde Haugedal</creatorcontrib><creatorcontrib>Brun, Johan G</creatorcontrib><creatorcontrib>Halse, Anne-Kristine</creatorcontrib><creatorcontrib>Jonsson, Roland</creatorcontrib><creatorcontrib>Fagerhol, Magne Kristoffer</creatorcontrib><creatorcontrib>Hammer, Hilde Berner</creatorcontrib><collection>NORA - Norwegian Open Research Archives</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Nordal, Hilde Haugedal</au><au>Brun, Johan G</au><au>Halse, Anne-Kristine</au><au>Jonsson, Roland</au><au>Fagerhol, Magne Kristoffer</au><au>Hammer, Hilde Berner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The neutrophil protein S100A12 is associated with a comprehensive ultrasonographic synovitis score in a longitudinal study of patients with rheumatoid arthritis treated with adalimumab</atitle><date>2014</date><risdate>2014</risdate><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 &lt; 0.01) and significant correlations were found between S100A12 and the other laboratory markers during follow-up (0.50-0.62, p &lt; 0.05). Of the clinical assessments, S100A12 had highest correlations with the assessor’s global VAS (0.46-0.85, p &lt; 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 &lt; 0.001)) for sum BM scores and 0.45 (0.27-0.75 (NS-p &lt; 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.</abstract><pub>BioMed Central</pub><oa>free_for_read</oa></addata></record>
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subjects Biologic therapy
Inflammation
Rheumatoid arthritis
S100 proteins
S100A12
Ultrasonography
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
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