Antibodies to Both Ro52 and Ro60 for Identifying Sjögren's Syndrome Patients Best Suited for Clinical Trials of Disease‐Modifying Therapies

Objective To assess anti‐Ro52 and anti‐Ro60 serologic profiles as markers of clinically relevant phenotypic subsets of patients with Sjögren's syndrome (SS). Methods From a cohort of 839 consecutive patients with suspected or established SS seen in our multidisciplinary SS center, we compared t...

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Veröffentlicht in:Arthritis care & research (2010) 2022-09, Vol.74 (9), p.1559-1565
Hauptverfasser: Armağan, Berkan, Robinson, Susan A., Bazoberry, Adriana, Perin, Jamie, Grader‐Beck, Thomas, Akpek, Esen K., Kim, Jean, Baer, Alan N.
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container_end_page 1565
container_issue 9
container_start_page 1559
container_title Arthritis care & research (2010)
container_volume 74
creator Armağan, Berkan
Robinson, Susan A.
Bazoberry, Adriana
Perin, Jamie
Grader‐Beck, Thomas
Akpek, Esen K.
Kim, Jean
Baer, Alan N.
description Objective To assess anti‐Ro52 and anti‐Ro60 serologic profiles as markers of clinically relevant phenotypic subsets of patients with Sjögren's syndrome (SS). Methods From a cohort of 839 consecutive patients with suspected or established SS seen in our multidisciplinary SS center, we compared the association of key phenotypic features in 390 patients who fulfilled SS classification criteria and in the parent cohort, stratifed by the presence of both anti‐Ro60 and anti‐Ro52, anti‐Ro60 alone, and anti‐Ro52 alone. Results The SS cohort included 227 patients (58%) with both anti‐Ro60 and anti‐Ro52, 65 (17%) with anti‐Ro60 alone, 58 (15%) with anti‐Ro52 alone, and 40 (10%) with neither antibody. Those with both anti‐Ro60 and anti‐Ro52 had a significantly increased prevalence of abnormal ocular surface staining, focal lymphocytic sialadenitis with focus score ≥1, antinuclear antibody ≥1:320, anti‐SSB/La, rheumatoid factor, and IgG ≥15.6 gm/liter (P 
doi_str_mv 10.1002/acr.24597
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Methods From a cohort of 839 consecutive patients with suspected or established SS seen in our multidisciplinary SS center, we compared the association of key phenotypic features in 390 patients who fulfilled SS classification criteria and in the parent cohort, stratifed by the presence of both anti‐Ro60 and anti‐Ro52, anti‐Ro60 alone, and anti‐Ro52 alone. Results The SS cohort included 227 patients (58%) with both anti‐Ro60 and anti‐Ro52, 65 (17%) with anti‐Ro60 alone, 58 (15%) with anti‐Ro52 alone, and 40 (10%) with neither antibody. Those with both anti‐Ro60 and anti‐Ro52 had a significantly increased prevalence of abnormal ocular surface staining, focal lymphocytic sialadenitis with focus score ≥1, antinuclear antibody ≥1:320, anti‐SSB/La, rheumatoid factor, and IgG ≥15.6 gm/liter (P &lt; 0.0016 for all). The groups with isolated anti‐Ro52 and anti‐Ro60 were equivalent to each other in their phenotypic associations, except for rheumatoid factor, which was higher in the anti‐Ro52 alone group. The associations of these Ro antibody serologic profiles were similar in the parent cohort, except for additional associations with salivary gland enlargement and parotid gland ultrasound score. Conclusion SS patients with both anti‐Ro60 and anti‐Ro52 antibodies are distinguished by a higher prevalence of markers of B‐cell hyperactivity and glandular inflammation. Antibody reactivity to both Ro60 and Ro52 may thus serve as an important inclusion criterion for SS patients in clinical trials where the therapeutic agent targets pathways mediating these pathogenic abnormalities.</description><identifier>ISSN: 2151-464X</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.24597</identifier><identifier>PMID: 33742788</identifier><language>eng</language><publisher>Boston, USA: Wiley Periodicals, Inc</publisher><subject>Antibodies ; Antinuclear antibodies ; Clinical trials ; Immunoglobulin G ; Parotid gland ; Patients ; Rheumatoid factor ; Salivary gland ; Sjogren's syndrome</subject><ispartof>Arthritis care &amp; research (2010), 2022-09, Vol.74 (9), p.1559-1565</ispartof><rights>2021 American College of Rheumatology.</rights><rights>2022 American College of Rheumatology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3887-3ce36caed5b9c774c40f766e18b296532ba5c9b67c4479d1873c6cde977782303</citedby><cites>FETCH-LOGICAL-c3887-3ce36caed5b9c774c40f766e18b296532ba5c9b67c4479d1873c6cde977782303</cites><orcidid>0000-0003-4409-059X ; 0000-0001-8344-013X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Facr.24597$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.24597$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33742788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Armağan, Berkan</creatorcontrib><creatorcontrib>Robinson, Susan A.</creatorcontrib><creatorcontrib>Bazoberry, Adriana</creatorcontrib><creatorcontrib>Perin, Jamie</creatorcontrib><creatorcontrib>Grader‐Beck, Thomas</creatorcontrib><creatorcontrib>Akpek, Esen K.</creatorcontrib><creatorcontrib>Kim, Jean</creatorcontrib><creatorcontrib>Baer, Alan N.</creatorcontrib><title>Antibodies to Both Ro52 and Ro60 for Identifying Sjögren's Syndrome Patients Best Suited for Clinical Trials of Disease‐Modifying Therapies</title><title>Arthritis care &amp; research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective To assess anti‐Ro52 and anti‐Ro60 serologic profiles as markers of clinically relevant phenotypic subsets of patients with Sjögren's syndrome (SS). Methods From a cohort of 839 consecutive patients with suspected or established SS seen in our multidisciplinary SS center, we compared the association of key phenotypic features in 390 patients who fulfilled SS classification criteria and in the parent cohort, stratifed by the presence of both anti‐Ro60 and anti‐Ro52, anti‐Ro60 alone, and anti‐Ro52 alone. Results The SS cohort included 227 patients (58%) with both anti‐Ro60 and anti‐Ro52, 65 (17%) with anti‐Ro60 alone, 58 (15%) with anti‐Ro52 alone, and 40 (10%) with neither antibody. Those with both anti‐Ro60 and anti‐Ro52 had a significantly increased prevalence of abnormal ocular surface staining, focal lymphocytic sialadenitis with focus score ≥1, antinuclear antibody ≥1:320, anti‐SSB/La, rheumatoid factor, and IgG ≥15.6 gm/liter (P &lt; 0.0016 for all). The groups with isolated anti‐Ro52 and anti‐Ro60 were equivalent to each other in their phenotypic associations, except for rheumatoid factor, which was higher in the anti‐Ro52 alone group. The associations of these Ro antibody serologic profiles were similar in the parent cohort, except for additional associations with salivary gland enlargement and parotid gland ultrasound score. Conclusion SS patients with both anti‐Ro60 and anti‐Ro52 antibodies are distinguished by a higher prevalence of markers of B‐cell hyperactivity and glandular inflammation. Antibody reactivity to both Ro60 and Ro52 may thus serve as an important inclusion criterion for SS patients in clinical trials where the therapeutic agent targets pathways mediating these pathogenic abnormalities.</description><subject>Antibodies</subject><subject>Antinuclear antibodies</subject><subject>Clinical trials</subject><subject>Immunoglobulin G</subject><subject>Parotid gland</subject><subject>Patients</subject><subject>Rheumatoid factor</subject><subject>Salivary gland</subject><subject>Sjogren's syndrome</subject><issn>2151-464X</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10T1uFDEYBmALgUgUUnABZIkCKDbx-H_KzfKTSEGg7CLRWR77m8Sr2fHGnhHajhMgTsMFuElOgpMJKZBw4694_PqTXoSeV-SoIoQeW5eOKBe1eoT2aSWqGZdCP36Y-dc9dJjzmpTDqNasfor2GFOcKq330Y95P4Qm-gAZDxGfxOEKX0RBse19GSTBbUz4zENh7S70l3i5_v3rMkH_KuPlrvcpbgB_tkMoIuMTyANejmEAf_dw0YU-ONvhVQq2yzi2-G3IYDPcfP_5sXw7Za6uINlt2eEZetIWB4f39wH68v7danE6O__04WwxP585prWaMQdMOgteNLVTijtOWiUlVLqhtRSMNla4upHKca5qX2nFnHQeaqWUpoywA_R6yt2meD2Wpc0mZAddZ3uIYzZUEMY54eKWvvyHruOY-rKdoYooVRMpRFFvJuVSzDlBa7YpbGzamYqY255M6cnc9VTsi_vEsdmAf5B_WyngeALfQge7_yeZ-eJiivwDlTedCg</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Armağan, Berkan</creator><creator>Robinson, Susan A.</creator><creator>Bazoberry, Adriana</creator><creator>Perin, Jamie</creator><creator>Grader‐Beck, Thomas</creator><creator>Akpek, Esen K.</creator><creator>Kim, Jean</creator><creator>Baer, Alan N.</creator><general>Wiley Periodicals, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4409-059X</orcidid><orcidid>https://orcid.org/0000-0001-8344-013X</orcidid></search><sort><creationdate>202209</creationdate><title>Antibodies to Both Ro52 and Ro60 for Identifying Sjögren's Syndrome Patients Best Suited for Clinical Trials of Disease‐Modifying Therapies</title><author>Armağan, Berkan ; Robinson, Susan A. ; Bazoberry, Adriana ; Perin, Jamie ; Grader‐Beck, Thomas ; Akpek, Esen K. ; Kim, Jean ; Baer, Alan N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-3ce36caed5b9c774c40f766e18b296532ba5c9b67c4479d1873c6cde977782303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Antinuclear antibodies</topic><topic>Clinical trials</topic><topic>Immunoglobulin G</topic><topic>Parotid gland</topic><topic>Patients</topic><topic>Rheumatoid factor</topic><topic>Salivary gland</topic><topic>Sjogren's syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Armağan, Berkan</creatorcontrib><creatorcontrib>Robinson, Susan A.</creatorcontrib><creatorcontrib>Bazoberry, Adriana</creatorcontrib><creatorcontrib>Perin, Jamie</creatorcontrib><creatorcontrib>Grader‐Beck, Thomas</creatorcontrib><creatorcontrib>Akpek, Esen K.</creatorcontrib><creatorcontrib>Kim, Jean</creatorcontrib><creatorcontrib>Baer, Alan N.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis care &amp; research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Armağan, Berkan</au><au>Robinson, Susan A.</au><au>Bazoberry, Adriana</au><au>Perin, Jamie</au><au>Grader‐Beck, Thomas</au><au>Akpek, Esen K.</au><au>Kim, Jean</au><au>Baer, Alan N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibodies to Both Ro52 and Ro60 for Identifying Sjögren's Syndrome Patients Best Suited for Clinical Trials of Disease‐Modifying Therapies</atitle><jtitle>Arthritis care &amp; research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2022-09</date><risdate>2022</risdate><volume>74</volume><issue>9</issue><spage>1559</spage><epage>1565</epage><pages>1559-1565</pages><issn>2151-464X</issn><eissn>2151-4658</eissn><abstract>Objective To assess anti‐Ro52 and anti‐Ro60 serologic profiles as markers of clinically relevant phenotypic subsets of patients with Sjögren's syndrome (SS). Methods From a cohort of 839 consecutive patients with suspected or established SS seen in our multidisciplinary SS center, we compared the association of key phenotypic features in 390 patients who fulfilled SS classification criteria and in the parent cohort, stratifed by the presence of both anti‐Ro60 and anti‐Ro52, anti‐Ro60 alone, and anti‐Ro52 alone. Results The SS cohort included 227 patients (58%) with both anti‐Ro60 and anti‐Ro52, 65 (17%) with anti‐Ro60 alone, 58 (15%) with anti‐Ro52 alone, and 40 (10%) with neither antibody. Those with both anti‐Ro60 and anti‐Ro52 had a significantly increased prevalence of abnormal ocular surface staining, focal lymphocytic sialadenitis with focus score ≥1, antinuclear antibody ≥1:320, anti‐SSB/La, rheumatoid factor, and IgG ≥15.6 gm/liter (P &lt; 0.0016 for all). The groups with isolated anti‐Ro52 and anti‐Ro60 were equivalent to each other in their phenotypic associations, except for rheumatoid factor, which was higher in the anti‐Ro52 alone group. The associations of these Ro antibody serologic profiles were similar in the parent cohort, except for additional associations with salivary gland enlargement and parotid gland ultrasound score. Conclusion SS patients with both anti‐Ro60 and anti‐Ro52 antibodies are distinguished by a higher prevalence of markers of B‐cell hyperactivity and glandular inflammation. Antibody reactivity to both Ro60 and Ro52 may thus serve as an important inclusion criterion for SS patients in clinical trials where the therapeutic agent targets pathways mediating these pathogenic abnormalities.</abstract><cop>Boston, USA</cop><pub>Wiley Periodicals, Inc</pub><pmid>33742788</pmid><doi>10.1002/acr.24597</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4409-059X</orcidid><orcidid>https://orcid.org/0000-0001-8344-013X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antibodies
Antinuclear antibodies
Clinical trials
Immunoglobulin G
Parotid gland
Patients
Rheumatoid factor
Salivary gland
Sjogren's syndrome
title Antibodies to Both Ro52 and Ro60 for Identifying Sjögren's Syndrome Patients Best Suited for Clinical Trials of Disease‐Modifying Therapies
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