Plasma calprotectin as a biomarker of ultrasound synovitis in rheumatoid arthritis patients receiving IL-6 antagonists or JAK inhibitors
Objectives: To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors (anti-rIL-6) or JAK inhibitors (JAKis) in detecting ultrasound (US) synovitis and compare it with acute phase reactants [high-sensitivity C-rea...
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Published in | Therapeutic advances in musculoskeletal disease Vol. 14; p. 1759720X221114105 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
2022
SAGE PUBLICATIONS, INC SAGE Publishing |
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Abstract | Objectives:
To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors (anti-rIL-6) or JAK inhibitors (JAKis) in detecting ultrasound (US) synovitis and compare it with acute phase reactants [high-sensitivity C-reactive protein (hs-CRP) and ESR].
Methods:
An observational cross-sectional study of RA patients receiving anti-rIL-6 (tocilizumab or sarilumab) or JAKi, (baricitinib or tofacitinib) was made. Plasma calprotectin for the diagnosis of US synovitis [synovial hypertrophy grade (SH) ⩾ 2 plus power Doppler signal (PD) ⩾ 1] was analysed using receiver operating characteristic curves (ROCs). The performance of ESR and hs-CRP was also studied. The three ROC curves were compared to determine which had the highest discriminatory power. Associations between plasma calprotectin and US scores were made using correlation analysis.
Results:
Sixty-three RA patients were included. Mean plasma calprotectin levels were significantly higher in patients with US synovitis than in those without (0.89 ± 0.85 vs 0.30 ± 0.12 μg/ml; p = 0.0003). A moderate correlation between calprotectin and all US scores (HS score Rho = 0.479; PD score Rho = 0.492; and global score Rho = 0.495) was found. The discriminatory capacity of plasma calprotectin showed an AUC of 0.795 (95% CI: 0.687–0.904). The AUC of hs-CRP and ESR was 0.721 and 0.564, respectively. hs-CRP serum levels showed a low positive correlation with the three US scores (Rho < 0.40). After analysis according to the drugs administered, the correlation disappeared in patients receiving anti-rIL-6.
Conclusion:
Plasma calprotectin may be a sensitive biomarker of synovial inflammation in RA patients treated with anti-rIL-6 or JAKi. |
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AbstractList | Objectives: To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors (anti-rIL-6) or JAK inhibitors (JAKis) in detecting ultrasound (US) synovitis and compare it with acute phase reactants [high-sensitivity C-reactive protein (hs-CRP) and ESR]. Methods: An observational cross-sectional study of RA patients receiving anti-rIL-6 (tocilizumab or sarilumab) or JAKi, (baricitinib or tofacitinib) was made. Plasma calprotectin for the diagnosis of US synovitis [synovial hypertrophy grade (SH) ⩾ 2 plus power Doppler signal (PD) ⩾ 1] was analysed using receiver operating characteristic curves (ROCs). The performance of ESR and hs-CRP was also studied. The three ROC curves were compared to determine which had the highest discriminatory power. Associations between plasma calprotectin and US scores were made using correlation analysis. Results: Sixty-three RA patients were included. Mean plasma calprotectin levels were significantly higher in patients with US synovitis than in those without (0.89 ± 0.85 vs 0.30 ± 0.12 μg/ml; p = 0.0003). A moderate correlation between calprotectin and all US scores (HS score Rho = 0.479; PD score Rho = 0.492; and global score Rho = 0.495) was found. The discriminatory capacity of plasma calprotectin showed an AUC of 0.795 (95% CI: 0.687–0.904). The AUC of hs-CRP and ESR was 0.721 and 0.564, respectively. hs-CRP serum levels showed a low positive correlation with the three US scores (Rho < 0.40). After analysis according to the drugs administered, the correlation disappeared in patients receiving anti-rIL-6. Conclusion: Plasma calprotectin may be a sensitive biomarker of synovial inflammation in RA patients treated with anti-rIL-6 or JAKi. Objectives: To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors (anti-rIL-6) or JAK inhibitors (JAKis) in detecting ultrasound (US) synovitis and compare it with acute phase reactants [high-sensitivity C-reactive protein (hs-CRP) and ESR]. Methods: An observational cross-sectional study of RA patients receiving anti-rIL-6 (tocilizumab or sarilumab) or JAKi, (baricitinib or tofacitinib) was made. Plasma calprotectin for the diagnosis of US synovitis [synovial hypertrophy grade (SH) ⩾ 2 plus power Doppler signal (PD) ⩾ 1] was analysed using receiver operating characteristic curves (ROCs). The performance of ESR and hs-CRP was also studied. The three ROC curves were compared to determine which had the highest discriminatory power. Associations between plasma calprotectin and US scores were made using correlation analysis. Results: Sixty-three RA patients were included. Mean plasma calprotectin levels were significantly higher in patients with US synovitis than in those without (0.89 ± 0.85 vs 0.30 ± 0.12 μg/ml; p = 0.0003). A moderate correlation between calprotectin and all US scores (HS score Rho = 0.479; PD score Rho = 0.492; and global score Rho = 0.495) was found. The discriminatory capacity of plasma calprotectin showed an AUC of 0.795 (95% CI: 0.687–0.904). The AUC of hs-CRP and ESR was 0.721 and 0.564, respectively. hs-CRP serum levels showed a low positive correlation with the three US scores (Rho < 0.40). After analysis according to the drugs administered, the correlation disappeared in patients receiving anti-rIL-6. Conclusion: Plasma calprotectin may be a sensitive biomarker of synovial inflammation in RA patients treated with anti-rIL-6 or JAKi. ObjectivesTo analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors (anti-rIL-6) or JAK inhibitors (JAKis) in detecting ultrasound (US) synovitis and compare it with acute phase reactants [high-sensitivity C-reactive protein (hs-CRP) and ESR]. MethodsAn observational cross-sectional study of RA patients receiving anti-rIL-6 (tocilizumab or sarilumab) or JAKi, (baricitinib or tofacitinib) was made. Plasma calprotectin for the diagnosis of US synovitis [synovial hypertrophy grade (SH) ⩾ 2 plus power Doppler signal (PD) ⩾ 1] was analysed using receiver operating characteristic curves (ROCs). The performance of ESR and hs-CRP was also studied. The three ROC curves were compared to determine which had the highest discriminatory power. Associations between plasma calprotectin and US scores were made using correlation analysis. ResultsSixty-three RA patients were included. Mean plasma calprotectin levels were significantly higher in patients with US synovitis than in those without (0.89 ± 0.85 vs 0.30 ± 0.12 μg/ml; p = 0.0003). A moderate correlation between calprotectin and all US scores (HS score Rho = 0.479; PD score Rho = 0.492; and global score Rho = 0.495) was found. The discriminatory capacity of plasma calprotectin showed an AUC of 0.795 (95% CI: 0.687-0.904). The AUC of hs-CRP and ESR was 0.721 and 0.564, respectively. hs-CRP serum levels showed a low positive correlation with the three US scores (Rho < 0.40). After analysis according to the drugs administered, the correlation disappeared in patients receiving anti-rIL-6. ConclusionPlasma calprotectin may be a sensitive biomarker of synovial inflammation in RA patients treated with anti-rIL-6 or JAKi. |
Author | Ruiz-Esquide, Viginia Yague, Jordi Ramirez, Julio Sanmarti, Raimon Ponce, Andrés Macías, Laura Morlà, Rosa Auge, Josep M. Gomez-Puerta, José A. Frade-Sosa, Beatriz Azuaga, Ana Belen Cañete, Juan D. Inciarte-Mundo, José |
Author_xml | – sequence: 1 givenname: Beatriz orcidid: 0000-0002-5867-8434 surname: Frade-Sosa fullname: Frade-Sosa, Beatriz organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 2 givenname: Andrés orcidid: 0000-0003-3068-5752 surname: Ponce fullname: Ponce, Andrés organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 3 givenname: José surname: Inciarte-Mundo fullname: Inciarte-Mundo, José organization: Fundació Clínic per a la Recerca Biomédica, Barcelona, Spain – sequence: 4 givenname: Rosa surname: Morlà fullname: Morlà, Rosa organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 5 givenname: Viginia orcidid: 0000-0002-2657-6601 surname: Ruiz-Esquide fullname: Ruiz-Esquide, Viginia organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 6 givenname: Laura surname: Macías fullname: Macías, Laura organization: Biochemistry and Molecular Genetics Department, Hospital Clínic of Barcelona, Barcelona, Spain – sequence: 7 givenname: Ana Belen surname: Azuaga fullname: Azuaga, Ana Belen organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 8 givenname: Julio surname: Ramirez fullname: Ramirez, Julio organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 9 givenname: Juan D. surname: Cañete fullname: Cañete, Juan D. organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 10 givenname: Jordi surname: Yague fullname: Yague, Jordi organization: Department of Immunology, Hospital Clinic – CDB, Barcelona, Spain – sequence: 11 givenname: Josep M. surname: Auge fullname: Auge, Josep M. organization: Biochemistry and Molecular Genetics Department, Hospital Clínic of Barcelona, Barcelona, Spain – sequence: 12 givenname: José A. orcidid: 0000-0001-8177-702X surname: Gomez-Puerta fullname: Gomez-Puerta, José A. organization: Department of Rheumatology, Hospital Clinic of Barcelona, Barcelona, Spain – sequence: 13 givenname: Raimon orcidid: 0000-0002-8864-3806 surname: Sanmarti fullname: Sanmarti, Raimon email: sanmarti@clinic.cat organization: Department of Rheumatology, Hospital Clinic of Barcelona, Carrer Villarroel 170, Barcelona 08170, Spain |
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CitedBy_id | crossref_primary_10_1016_j_reuma_2023_08_001 crossref_primary_10_1016_j_reumae_2023_10_002 crossref_primary_10_1007_s40744_024_00650_9 crossref_primary_10_3390_cancers15112984 |
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Keywords | acute phase proteins leukocyte L1 antigen complex (calprotectin) ultrasonography rheumatoid arthritis biomarkers |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Beatriz Frade-Sosa and Andres Ponce contributed equally. |
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finger and toe joints in rheumatoid arthritis publication-title: Arthritis Rheum contributor: fullname: Jacobsen – volume: 622 start-page: 105 year: 2020 article-title: Serum calprotectin: a promising biomarker in rheumatoid arthritis and axial spondyloarthritis publication-title: Arthritis Res Ther contributor: fullname: Lamacchia – volume: 79 start-page: 685 year: 2020 end-page: 699 article-title: EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update publication-title: Ann Rheum Dis contributor: fullname: Bijlsma – volume: 74 start-page: 499 year: 2015 end-page: 505 article-title: MRP8/14 serum levels as a strong predictor of response to biological treatments in patients with rheumatoid arthritis publication-title: Ann Rheum Dis contributor: fullname: Herenius – volume: 17 start-page: 252 year: 2015 article-title: Serum calprotectin (S100A8/9): an independent predictor of ultrasound synovitis in patients with rheumatoid arthritis publication-title: Arthritis Res Ther contributor: fullname: Hanova – volume: 60 start-page: 641 year: 2001 end-page: 649 article-title: Guidelines for musculoskeletal ultrasound in rheumatology publication-title: Ann Rheum Dis contributor: fullname: Gerber – volume: 16 start-page: 1 year: 2014 end-page: 10 article-title: Patients with rheumatoid arthritis in clinical remission and ultrasound-defined active synovitis exhibit higher disease activity and increased serum levels of angiogenic biomarkers publication-title: Arthritis Res Ther contributor: fullname: Pomés – ident: bibr1-1759720X221114105 doi: 10.1136/annrheumdis-2019-216655 – ident: bibr9-1759720X221114105 doi: 10.1136/ard.2006.064741 – ident: bibr24-1759720X221114105 doi: 10.7326/0003-4819-147-8-200710160-00010 – ident: bibr14-1759720X221114105 doi: 10.1002/art.22190 – ident: bibr23-1759720X221114105 doi: 10.1186/ar4431 – ident: bibr29-1759720X221114105 doi: 10.1016/j.jbspin.2019.01.003 – volume: 26 start-page: 2523 year: 1999 ident: bibr8-1759720X221114105 publication-title: J Rheumatol contributor: fullname: Youssef P – volume: 54 start-page: 2239 year: 2015 ident: bibr17-1759720X221114105 publication-title: Rheumatology (Oxford) contributor: fullname: Inciarte-Mundo J – ident: bibr11-1759720X221114105 doi: 10.1136/annrheumdis-2013-203923 – ident: bibr31-1759720X221114105 doi: 10.1186/s13075-016-1201-0 – ident: bibr3-1759720X221114105 doi: 10.1093/rheumatology/key225 – ident: bibr6-1759720X221114105 doi: 10.1002/art.27740 – ident: bibr27-1759720X221114105 doi: 10.1186/s13075-017-1346-5 – ident: bibr19-1759720X221114105 doi: 10.1136/ard.2010.138461 – ident: bibr15-1759720X221114105 doi: 10.1186/ar3503 – ident: bibr12-1759720X221114105 doi: 10.1186/s13075-018-1764-z – ident: bibr16-1759720X221114105 doi: 10.1186/s13075-016-1032-z – volume: 32 start-page: 2485 year: 2005 ident: bibr21-1759720X221114105 publication-title: J Rheumatol contributor: fullname: Wakefield RJ – ident: bibr28-1759720X221114105 doi: 10.2174/156652413804486214 – volume: 11 year: 2021 ident: bibr25-1759720X221114105 publication-title: Rheumatology (Oxford) contributor: fullname: Burmester GR – ident: bibr2-1759720X221114105 doi: 10.1016/j.semarthrit.2013.08.001 – ident: bibr32-1759720X221114105 doi: 10.1186/s13075-015-0764-5 – ident: bibr7-1759720X221114105 doi: 10.1038/s41584-018-0058-9 – volume: 30 start-page: 1426 year: 2003 ident: bibr26-1759720X221114105 publication-title: J Rheumatol contributor: fullname: Nishimoto N – ident: bibr30-1759720X221114105 doi: 10.1002/acr.22795 – ident: bibr22-1759720X221114105 doi: 10.1002/art.10877 – ident: bibr13-1759720X221114105 doi: 10.1016/j.semarthrit.2006.04.009 – ident: bibr10-1759720X221114105 doi: 10.1136/ard.2008.103739 – ident: bibr4-1759720X221114105 doi: 10.1186/ar565 – ident: bibr20-1759720X221114105 doi: 10.1136/ard.60.7.641 – ident: bibr5-1759720X221114105 doi: 10.1007/s10067-021-05815-3 – ident: bibr18-1759720X221114105 doi: 10.1186/s13075-020-02190-3 |
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To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors... Objectives: To analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors... ObjectivesTo analyse the accuracy of plasma calprotectin in patients with rheumatoid arthritis (RA) receiving monoclonal antibodies against IL-6 receptors... |
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SubjectTerms | Biomarkers Monoclonal antibodies Musculoskeletal diseases Original Research Plasma Rheumatoid arthritis Ultrasonic imaging |
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Title | Plasma calprotectin as a biomarker of ultrasound synovitis in rheumatoid arthritis patients receiving IL-6 antagonists or JAK inhibitors |
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