B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome

Abstract Objectives B-cell activating factor (BAFF), β-2 microglobulin (β2M) and serum free light chains (FLCs) are elevated in primary SS (pSS) and associated with disease activity. We aimed to investigate their association with the individual disease activity domains of the EULAR Sjögren's Sy...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2018-07, Vol.57 (7), p.1222-1227
Hauptverfasser: James, Katherine, Chipeta, Chimwemwe, Parker, Antony, Harding, Stephen, Cockell, Simon J, Gillespie, Colin S, Hallinan, Jennifer, Barone, Francesca, Bowman, Simon J, Ng, Wan-Fai, Fisher, Benjamin A
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container_end_page 1227
container_issue 7
container_start_page 1222
container_title Rheumatology (Oxford, England)
container_volume 57
creator James, Katherine
Chipeta, Chimwemwe
Parker, Antony
Harding, Stephen
Cockell, Simon J
Gillespie, Colin S
Hallinan, Jennifer
Barone, Francesca
Bowman, Simon J
Ng, Wan-Fai
Fisher, Benjamin A
description Abstract Objectives B-cell activating factor (BAFF), β-2 microglobulin (β2M) and serum free light chains (FLCs) are elevated in primary SS (pSS) and associated with disease activity. We aimed to investigate their association with the individual disease activity domains of the EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) in a large well-characterized pSS cohort. Methods Sera from pSS patients enrolled in the UK Primary Sjögren's Syndrome Registry (UKPSSR) (n = 553) and healthy controls (n = 286) were analysed for FLC (κ and λ), BAFF and β2 M. Pearson correlation coefficients were calculated for patient clinical characteristics, including salivary flow, Schirmer's test, EULAR Sjögren's Syndrome Patient Reported Index and serum IgG levels. Poisson regression was performed to identify independent predictors of total ESSDAI and ClinESSDAI (validated ESSDAI minus the biological domain) scores and their domains. Results Levels of BAFF, β2M and FLCs were higher in pSS patients compared to controls. All three biomarkers associated significantly with the ESSDAI and the ClinESSDAI. BAFF associated with the peripheral nervous system domain of the ESSDAI, whereas β2M and FLCs associated with the cutaneous, biological and renal domains. Multivariate analysis showed BAFF, β2M and their interaction to be independent predictors of ESSDAI/ClinESSDAI. FLCs were also shown to associate with the ESSDAI/ClinESSDAI but not independent of serum IgG. Conclusion All biomarkers were associated with total ESSDAI scores but with differing domain associations. These findings should encourage further investigation of these biomarkers in longitudinal studies and against other disease activity measures.
doi_str_mv 10.1093/rheumatology/key063
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We aimed to investigate their association with the individual disease activity domains of the EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) in a large well-characterized pSS cohort. Methods Sera from pSS patients enrolled in the UK Primary Sjögren's Syndrome Registry (UKPSSR) (n = 553) and healthy controls (n = 286) were analysed for FLC (κ and λ), BAFF and β2 M. Pearson correlation coefficients were calculated for patient clinical characteristics, including salivary flow, Schirmer's test, EULAR Sjögren's Syndrome Patient Reported Index and serum IgG levels. Poisson regression was performed to identify independent predictors of total ESSDAI and ClinESSDAI (validated ESSDAI minus the biological domain) scores and their domains. Results Levels of BAFF, β2M and FLCs were higher in pSS patients compared to controls. All three biomarkers associated significantly with the ESSDAI and the ClinESSDAI. BAFF associated with the peripheral nervous system domain of the ESSDAI, whereas β2M and FLCs associated with the cutaneous, biological and renal domains. Multivariate analysis showed BAFF, β2M and their interaction to be independent predictors of ESSDAI/ClinESSDAI. FLCs were also shown to associate with the ESSDAI/ClinESSDAI but not independent of serum IgG. Conclusion All biomarkers were associated with total ESSDAI scores but with differing domain associations. These findings should encourage further investigation of these biomarkers in longitudinal studies and against other disease activity measures.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/key063</identifier><identifier>PMID: 29608774</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Biomarkers ; BLyS protein ; Clinical Science ; Immunoglobulin G ; Light chains ; Lymphocytes B ; Multivariate analysis ; Nervous system ; Sjogren's syndrome</subject><ispartof>Rheumatology (Oxford, England), 2018-07, Vol.57 (7), p.1222-1227</ispartof><rights>The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. 2018</rights><rights>The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-5762dd5488f8c7d9e45484fdc86d189f48c162269c67a6214af85e746563d07c3</citedby><cites>FETCH-LOGICAL-c472t-5762dd5488f8c7d9e45484fdc86d189f48c162269c67a6214af85e746563d07c3</cites><orcidid>0000-0003-4631-549X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29608774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>James, Katherine</creatorcontrib><creatorcontrib>Chipeta, Chimwemwe</creatorcontrib><creatorcontrib>Parker, Antony</creatorcontrib><creatorcontrib>Harding, Stephen</creatorcontrib><creatorcontrib>Cockell, Simon J</creatorcontrib><creatorcontrib>Gillespie, Colin S</creatorcontrib><creatorcontrib>Hallinan, Jennifer</creatorcontrib><creatorcontrib>Barone, Francesca</creatorcontrib><creatorcontrib>Bowman, Simon J</creatorcontrib><creatorcontrib>Ng, Wan-Fai</creatorcontrib><creatorcontrib>Fisher, Benjamin A</creatorcontrib><creatorcontrib>UK Primary Sjögren’s Syndrome Registry</creatorcontrib><title>B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Abstract Objectives B-cell activating factor (BAFF), β-2 microglobulin (β2M) and serum free light chains (FLCs) are elevated in primary SS (pSS) and associated with disease activity. We aimed to investigate their association with the individual disease activity domains of the EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) in a large well-characterized pSS cohort. Methods Sera from pSS patients enrolled in the UK Primary Sjögren's Syndrome Registry (UKPSSR) (n = 553) and healthy controls (n = 286) were analysed for FLC (κ and λ), BAFF and β2 M. Pearson correlation coefficients were calculated for patient clinical characteristics, including salivary flow, Schirmer's test, EULAR Sjögren's Syndrome Patient Reported Index and serum IgG levels. Poisson regression was performed to identify independent predictors of total ESSDAI and ClinESSDAI (validated ESSDAI minus the biological domain) scores and their domains. Results Levels of BAFF, β2M and FLCs were higher in pSS patients compared to controls. All three biomarkers associated significantly with the ESSDAI and the ClinESSDAI. BAFF associated with the peripheral nervous system domain of the ESSDAI, whereas β2M and FLCs associated with the cutaneous, biological and renal domains. Multivariate analysis showed BAFF, β2M and their interaction to be independent predictors of ESSDAI/ClinESSDAI. FLCs were also shown to associate with the ESSDAI/ClinESSDAI but not independent of serum IgG. Conclusion All biomarkers were associated with total ESSDAI scores but with differing domain associations. These findings should encourage further investigation of these biomarkers in longitudinal studies and against other disease activity measures.</description><subject>Biomarkers</subject><subject>BLyS protein</subject><subject>Clinical Science</subject><subject>Immunoglobulin G</subject><subject>Light chains</subject><subject>Lymphocytes B</subject><subject>Multivariate analysis</subject><subject>Nervous system</subject><subject>Sjogren's syndrome</subject><issn>1462-0324</issn><issn>1462-0332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkc2O0zAUhS0EYsrAEyCNLLGATTr-i-NskIYRf9JILIC1Zeyb1m0Sd-ykKC_GC_BiuEophRUrX8nfPTrnHoSeU7KkpObXcQ1jZ4bQhtV0vYWJSP4ALaiQrCCcs4enmYkL9CSlDSGkpFw9RheslkRVlVig7k1hoW2xsYPf-2HCnYlbiAmbCNikFKw3Azj83Q9r7HzTQIR-yFMCk-DPmgud8X3Cvse76LPIhD9vfv5YZfplwmnqXQwdPEWPGtMmeHZ8L9HXd2-_3H4o7j69_3h7c1dYUbGhKCvJnCuFUo2ylatB5Fk0zirpqKoboSyVjMnayspIRoVpVAmVkKXkjlSWX6LXs-5u_NaBs9lyNK0-OtPBeP33T-_XehX2WhIqqOBZ4NVRIIb7EdKgO58OhzI9hDFpRhjlVClaZvTFP-gmjLHP8TTjRB5SlHWm-EzZGFKK0JzMUKIPderzOvVcZ966Os9x2vndXwaWMxDG3X8p_gIUDLOp</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>James, Katherine</creator><creator>Chipeta, Chimwemwe</creator><creator>Parker, Antony</creator><creator>Harding, Stephen</creator><creator>Cockell, Simon J</creator><creator>Gillespie, Colin S</creator><creator>Hallinan, Jennifer</creator><creator>Barone, Francesca</creator><creator>Bowman, Simon J</creator><creator>Ng, Wan-Fai</creator><creator>Fisher, Benjamin A</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4631-549X</orcidid></search><sort><creationdate>20180701</creationdate><title>B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome</title><author>James, Katherine ; Chipeta, Chimwemwe ; Parker, Antony ; Harding, Stephen ; Cockell, Simon J ; Gillespie, Colin S ; Hallinan, Jennifer ; Barone, Francesca ; Bowman, Simon J ; Ng, Wan-Fai ; Fisher, Benjamin A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-5762dd5488f8c7d9e45484fdc86d189f48c162269c67a6214af85e746563d07c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biomarkers</topic><topic>BLyS protein</topic><topic>Clinical Science</topic><topic>Immunoglobulin G</topic><topic>Light chains</topic><topic>Lymphocytes B</topic><topic>Multivariate analysis</topic><topic>Nervous system</topic><topic>Sjogren's syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>James, Katherine</creatorcontrib><creatorcontrib>Chipeta, Chimwemwe</creatorcontrib><creatorcontrib>Parker, Antony</creatorcontrib><creatorcontrib>Harding, Stephen</creatorcontrib><creatorcontrib>Cockell, Simon J</creatorcontrib><creatorcontrib>Gillespie, Colin S</creatorcontrib><creatorcontrib>Hallinan, Jennifer</creatorcontrib><creatorcontrib>Barone, Francesca</creatorcontrib><creatorcontrib>Bowman, Simon J</creatorcontrib><creatorcontrib>Ng, Wan-Fai</creatorcontrib><creatorcontrib>Fisher, Benjamin A</creatorcontrib><creatorcontrib>UK Primary Sjögren’s Syndrome Registry</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>James, Katherine</au><au>Chipeta, Chimwemwe</au><au>Parker, Antony</au><au>Harding, Stephen</au><au>Cockell, Simon J</au><au>Gillespie, Colin S</au><au>Hallinan, Jennifer</au><au>Barone, Francesca</au><au>Bowman, Simon J</au><au>Ng, Wan-Fai</au><au>Fisher, Benjamin A</au><aucorp>UK Primary Sjögren’s Syndrome Registry</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>57</volume><issue>7</issue><spage>1222</spage><epage>1227</epage><pages>1222-1227</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><abstract>Abstract Objectives B-cell activating factor (BAFF), β-2 microglobulin (β2M) and serum free light chains (FLCs) are elevated in primary SS (pSS) and associated with disease activity. We aimed to investigate their association with the individual disease activity domains of the EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) in a large well-characterized pSS cohort. Methods Sera from pSS patients enrolled in the UK Primary Sjögren's Syndrome Registry (UKPSSR) (n = 553) and healthy controls (n = 286) were analysed for FLC (κ and λ), BAFF and β2 M. Pearson correlation coefficients were calculated for patient clinical characteristics, including salivary flow, Schirmer's test, EULAR Sjögren's Syndrome Patient Reported Index and serum IgG levels. Poisson regression was performed to identify independent predictors of total ESSDAI and ClinESSDAI (validated ESSDAI minus the biological domain) scores and their domains. Results Levels of BAFF, β2M and FLCs were higher in pSS patients compared to controls. All three biomarkers associated significantly with the ESSDAI and the ClinESSDAI. BAFF associated with the peripheral nervous system domain of the ESSDAI, whereas β2M and FLCs associated with the cutaneous, biological and renal domains. Multivariate analysis showed BAFF, β2M and their interaction to be independent predictors of ESSDAI/ClinESSDAI. FLCs were also shown to associate with the ESSDAI/ClinESSDAI but not independent of serum IgG. Conclusion All biomarkers were associated with total ESSDAI scores but with differing domain associations. These findings should encourage further investigation of these biomarkers in longitudinal studies and against other disease activity measures.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>29608774</pmid><doi>10.1093/rheumatology/key063</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-4631-549X</orcidid><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects Biomarkers
BLyS protein
Clinical Science
Immunoglobulin G
Light chains
Lymphocytes B
Multivariate analysis
Nervous system
Sjogren's syndrome
title B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome
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