Association of CXCL13 serum level and ultrasonographic findings of joints in patients with systemic lupus erythematosus and Jaccoud’s arthropathy

Objectives The objective of this paper is to perform an ultrasonography (US) analysis of hands and wrists in two groups of patients with systemic lupus erythematosus (SLE), with and without Jaccoud’s arthropathy, matched by age and disease duration and to correlate them with levels of CXCL13 clinica...

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Veröffentlicht in:Lupus 2018-05, Vol.27 (6), p.939-946
Hauptverfasser: Ribeiro, D Sá, Lins, C F, Galvão, V, Santos, W G Dourado, Rosa, G, Machicado, V, Pedreira, A L, da Fonseca, E P, Souza, A P Mota Duque, Baleeiro, C, Ferreira, L G, Oliveira, I Silva de, Gama da Silva, J P Cotrim, Atta, A M, Santiago, M B
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container_end_page 946
container_issue 6
container_start_page 939
container_title Lupus
container_volume 27
creator Ribeiro, D Sá
Lins, C F
Galvão, V
Santos, W G Dourado
Rosa, G
Machicado, V
Pedreira, A L
da Fonseca, E P
Souza, A P Mota Duque
Baleeiro, C
Ferreira, L G
Oliveira, I Silva de
Gama da Silva, J P Cotrim
Atta, A M
Santiago, M B
description Objectives The objective of this paper is to perform an ultrasonography (US) analysis of hands and wrists in two groups of patients with systemic lupus erythematosus (SLE), with and without Jaccoud’s arthropathy, matched by age and disease duration and to correlate them with levels of CXCL13 clinical features, laboratory tests and disease activity score. Methods Sixty-four patients with SLE were enrolled, 32 with and 32 without Jaccoud’s arthropathy. Each patient underwent physical examination, laboratory tests (including CXCL13 by ELISA) and bilateral US. Synovial hypertrophy, tenosynovitis and erosions were evaluated according to a semiquantitative grading system with a 0–3 rating. US findings were correlated with serum levels of CXCL13, other serological parameters and disease activity index. Results Synovitis was found in 25/64 patients (39%) and tenosynovitis in 14/64 (22%). These findings were more frequent in SLE patients with Jaccoud’s arthropathy, particularly tenosynovitis (p = 0.002) and synovitis (p = 0.01). Median serum level of CXCL13 was 20.16 pg/ml in the whole population (23.21 pg/ml in the Jaccoud’s arthropathy group and 11.48 pg/ml in the group without). There was an association between the presence of disease activity and high level of CXCL13 (p = 0.004). However, no association was found between high levels of CXCL13 and “arthritis” in SLEDAI, swollen joints on physical examination or synovitis on US. Conclusions US findings in joints of SLE patients with Jaccoud’s arthropathy confirm that synovitis and tenosynovitis are common in these patients. In addition, serum level of CXCL13 is associated with disease activity in SLE but does not seem to be a biomarker for arthritis in these patients.
doi_str_mv 10.1177/0961203317753557
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Methods Sixty-four patients with SLE were enrolled, 32 with and 32 without Jaccoud’s arthropathy. Each patient underwent physical examination, laboratory tests (including CXCL13 by ELISA) and bilateral US. Synovial hypertrophy, tenosynovitis and erosions were evaluated according to a semiquantitative grading system with a 0–3 rating. US findings were correlated with serum levels of CXCL13, other serological parameters and disease activity index. Results Synovitis was found in 25/64 patients (39%) and tenosynovitis in 14/64 (22%). These findings were more frequent in SLE patients with Jaccoud’s arthropathy, particularly tenosynovitis (p = 0.002) and synovitis (p = 0.01). Median serum level of CXCL13 was 20.16 pg/ml in the whole population (23.21 pg/ml in the Jaccoud’s arthropathy group and 11.48 pg/ml in the group without). There was an association between the presence of disease activity and high level of CXCL13 (p = 0.004). However, no association was found between high levels of CXCL13 and “arthritis” in SLEDAI, swollen joints on physical examination or synovitis on US. Conclusions US findings in joints of SLE patients with Jaccoud’s arthropathy confirm that synovitis and tenosynovitis are common in these patients. In addition, serum level of CXCL13 is associated with disease activity in SLE but does not seem to be a biomarker for arthritis in these patients.</description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1177/0961203317753557</identifier><identifier>PMID: 29338586</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Arthritis ; Biomarkers ; CXCL13 protein ; Enzyme-linked immunosorbent assay ; Health risk assessment ; Hypertrophy ; Joint diseases ; Laboratories ; Lupus ; Serum levels ; Synovitis ; Systemic lupus erythematosus ; Tenosynovitis ; Ultrasound</subject><ispartof>Lupus, 2018-05, Vol.27 (6), p.939-946</ispartof><rights>The Author(s) 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-3077e4ae23dd4812263906f44c08a82747c6b9c19ad211d66dd631ffb9f69c653</citedby><cites>FETCH-LOGICAL-c365t-3077e4ae23dd4812263906f44c08a82747c6b9c19ad211d66dd631ffb9f69c653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0961203317753557$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0961203317753557$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,782,786,21828,27933,27934,43630,43631</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29338586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ribeiro, D Sá</creatorcontrib><creatorcontrib>Lins, C F</creatorcontrib><creatorcontrib>Galvão, V</creatorcontrib><creatorcontrib>Santos, W G Dourado</creatorcontrib><creatorcontrib>Rosa, G</creatorcontrib><creatorcontrib>Machicado, V</creatorcontrib><creatorcontrib>Pedreira, A L</creatorcontrib><creatorcontrib>da Fonseca, E P</creatorcontrib><creatorcontrib>Souza, A P Mota Duque</creatorcontrib><creatorcontrib>Baleeiro, C</creatorcontrib><creatorcontrib>Ferreira, L G</creatorcontrib><creatorcontrib>Oliveira, I Silva de</creatorcontrib><creatorcontrib>Gama da Silva, J P Cotrim</creatorcontrib><creatorcontrib>Atta, A M</creatorcontrib><creatorcontrib>Santiago, M B</creatorcontrib><title>Association of CXCL13 serum level and ultrasonographic findings of joints in patients with systemic lupus erythematosus and Jaccoud’s arthropathy</title><title>Lupus</title><addtitle>Lupus</addtitle><description>Objectives The objective of this paper is to perform an ultrasonography (US) analysis of hands and wrists in two groups of patients with systemic lupus erythematosus (SLE), with and without Jaccoud’s arthropathy, matched by age and disease duration and to correlate them with levels of CXCL13 clinical features, laboratory tests and disease activity score. Methods Sixty-four patients with SLE were enrolled, 32 with and 32 without Jaccoud’s arthropathy. Each patient underwent physical examination, laboratory tests (including CXCL13 by ELISA) and bilateral US. Synovial hypertrophy, tenosynovitis and erosions were evaluated according to a semiquantitative grading system with a 0–3 rating. US findings were correlated with serum levels of CXCL13, other serological parameters and disease activity index. Results Synovitis was found in 25/64 patients (39%) and tenosynovitis in 14/64 (22%). These findings were more frequent in SLE patients with Jaccoud’s arthropathy, particularly tenosynovitis (p = 0.002) and synovitis (p = 0.01). Median serum level of CXCL13 was 20.16 pg/ml in the whole population (23.21 pg/ml in the Jaccoud’s arthropathy group and 11.48 pg/ml in the group without). There was an association between the presence of disease activity and high level of CXCL13 (p = 0.004). However, no association was found between high levels of CXCL13 and “arthritis” in SLEDAI, swollen joints on physical examination or synovitis on US. Conclusions US findings in joints of SLE patients with Jaccoud’s arthropathy confirm that synovitis and tenosynovitis are common in these patients. In addition, serum level of CXCL13 is associated with disease activity in SLE but does not seem to be a biomarker for arthritis in these patients.</description><subject>Arthritis</subject><subject>Biomarkers</subject><subject>CXCL13 protein</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Health risk assessment</subject><subject>Hypertrophy</subject><subject>Joint diseases</subject><subject>Laboratories</subject><subject>Lupus</subject><subject>Serum levels</subject><subject>Synovitis</subject><subject>Systemic lupus erythematosus</subject><subject>Tenosynovitis</subject><subject>Ultrasound</subject><issn>0961-2033</issn><issn>1477-0962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc2OFCEUhYnROO3o3pUhceOmFIoqKJaTjr_pxI0m7io0UF10qqDkgqZ3vsOs5vV8Eil71GQSV9zL_c65hIPQU0peUirEKyI5rQljpW5Z24p7aEMbIapyX99Hm3VcrfML9AjgSAhhVPKH6KKWjHVtxzfo-gogaKeSCx6HAW-_bHeUYbAxz3iy3-yElTc4TykqCD4colpGp_HgvHH-AKvmGJxPgJ3HS_Gxa_3dpRHDCZKdCzzlJQO28ZRGO6sUoHSr6weldcjm54-b0sc0xlAMxtNj9GBQE9gnt-cl-vzm9aftu2r38e377dWu0oy3qWJECNsoWzNjmo7WNWeS8KFpNOlUV4tGaL6XmkplakoN58ZwRodhLwcuNW_ZJXpx9l1i-JotpH52oO00KW9Dhp7KTrZC0t_o8zvoMeToy-v68r-cS9lQUShypnQMANEO_RLdrOKpp6RfA-vvBlYkz26N83625q_gT0IFqM4AqIP9t_W_hr8A1vCgCA</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Ribeiro, D Sá</creator><creator>Lins, C F</creator><creator>Galvão, V</creator><creator>Santos, W G Dourado</creator><creator>Rosa, G</creator><creator>Machicado, V</creator><creator>Pedreira, A L</creator><creator>da Fonseca, E P</creator><creator>Souza, A P Mota Duque</creator><creator>Baleeiro, C</creator><creator>Ferreira, L G</creator><creator>Oliveira, I Silva de</creator><creator>Gama da Silva, J P Cotrim</creator><creator>Atta, A M</creator><creator>Santiago, M B</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20180501</creationdate><title>Association of CXCL13 serum level and ultrasonographic findings of joints in patients with systemic lupus erythematosus and Jaccoud’s arthropathy</title><author>Ribeiro, D Sá ; Lins, C F ; Galvão, V ; Santos, W G Dourado ; Rosa, G ; Machicado, V ; Pedreira, A L ; da Fonseca, E P ; Souza, A P Mota Duque ; Baleeiro, C ; Ferreira, L G ; Oliveira, I Silva de ; Gama da Silva, J P Cotrim ; Atta, A M ; Santiago, M B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-3077e4ae23dd4812263906f44c08a82747c6b9c19ad211d66dd631ffb9f69c653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Arthritis</topic><topic>Biomarkers</topic><topic>CXCL13 protein</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Health risk assessment</topic><topic>Hypertrophy</topic><topic>Joint diseases</topic><topic>Laboratories</topic><topic>Lupus</topic><topic>Serum levels</topic><topic>Synovitis</topic><topic>Systemic lupus erythematosus</topic><topic>Tenosynovitis</topic><topic>Ultrasound</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ribeiro, D Sá</creatorcontrib><creatorcontrib>Lins, C F</creatorcontrib><creatorcontrib>Galvão, V</creatorcontrib><creatorcontrib>Santos, W G Dourado</creatorcontrib><creatorcontrib>Rosa, G</creatorcontrib><creatorcontrib>Machicado, V</creatorcontrib><creatorcontrib>Pedreira, A L</creatorcontrib><creatorcontrib>da Fonseca, E P</creatorcontrib><creatorcontrib>Souza, A P Mota Duque</creatorcontrib><creatorcontrib>Baleeiro, C</creatorcontrib><creatorcontrib>Ferreira, L G</creatorcontrib><creatorcontrib>Oliveira, I Silva de</creatorcontrib><creatorcontrib>Gama da Silva, J P Cotrim</creatorcontrib><creatorcontrib>Atta, A M</creatorcontrib><creatorcontrib>Santiago, M B</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ribeiro, D Sá</au><au>Lins, C F</au><au>Galvão, V</au><au>Santos, W G Dourado</au><au>Rosa, G</au><au>Machicado, V</au><au>Pedreira, A L</au><au>da Fonseca, E P</au><au>Souza, A P Mota Duque</au><au>Baleeiro, C</au><au>Ferreira, L G</au><au>Oliveira, I Silva de</au><au>Gama da Silva, J P Cotrim</au><au>Atta, A M</au><au>Santiago, M B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of CXCL13 serum level and ultrasonographic findings of joints in patients with systemic lupus erythematosus and Jaccoud’s arthropathy</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2018-05-01</date><risdate>2018</risdate><volume>27</volume><issue>6</issue><spage>939</spage><epage>946</epage><pages>939-946</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract>Objectives The objective of this paper is to perform an ultrasonography (US) analysis of hands and wrists in two groups of patients with systemic lupus erythematosus (SLE), with and without Jaccoud’s arthropathy, matched by age and disease duration and to correlate them with levels of CXCL13 clinical features, laboratory tests and disease activity score. Methods Sixty-four patients with SLE were enrolled, 32 with and 32 without Jaccoud’s arthropathy. Each patient underwent physical examination, laboratory tests (including CXCL13 by ELISA) and bilateral US. Synovial hypertrophy, tenosynovitis and erosions were evaluated according to a semiquantitative grading system with a 0–3 rating. US findings were correlated with serum levels of CXCL13, other serological parameters and disease activity index. Results Synovitis was found in 25/64 patients (39%) and tenosynovitis in 14/64 (22%). These findings were more frequent in SLE patients with Jaccoud’s arthropathy, particularly tenosynovitis (p = 0.002) and synovitis (p = 0.01). Median serum level of CXCL13 was 20.16 pg/ml in the whole population (23.21 pg/ml in the Jaccoud’s arthropathy group and 11.48 pg/ml in the group without). There was an association between the presence of disease activity and high level of CXCL13 (p = 0.004). However, no association was found between high levels of CXCL13 and “arthritis” in SLEDAI, swollen joints on physical examination or synovitis on US. Conclusions US findings in joints of SLE patients with Jaccoud’s arthropathy confirm that synovitis and tenosynovitis are common in these patients. In addition, serum level of CXCL13 is associated with disease activity in SLE but does not seem to be a biomarker for arthritis in these patients.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29338586</pmid><doi>10.1177/0961203317753557</doi><tpages>8</tpages></addata></record>
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subjects Arthritis
Biomarkers
CXCL13 protein
Enzyme-linked immunosorbent assay
Health risk assessment
Hypertrophy
Joint diseases
Laboratories
Lupus
Serum levels
Synovitis
Systemic lupus erythematosus
Tenosynovitis
Ultrasound
title Association of CXCL13 serum level and ultrasonographic findings of joints in patients with systemic lupus erythematosus and Jaccoud’s arthropathy
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