<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Chalan P</submitter><pubmed_abstract>Presence of autoantibodies precedes development of seropositive rheumatoid arthritis (SP RA) and seropositive arthralgia patients (SAP) are at risk of developing RA. The aims of the study are to identify additional serum immune markers discriminating between SP and seronegative (SN) RA, and markers identifying high-risk SAP. Sera from SAP (n = 27), SP RA (n = 22), SN RA (n = 11) and healthy controls (n = 20) were analyzed using the Human Cytokine 25-Plex Panel. Selected markers were validated in independent cohorts of SP RA (n = 35) and SN RA (n = 12) patients. Eleven of 27 SAP developed RA within 8 months (median follow-up time, range 1-32 months), and their baseline serum markers were compared to 16 non-progressing SAP. SAP and SP RA patients showed a marked overlap in their systemic imm</pubmed_abstract><journal>Scientific reports</journal><pagination>26021</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4870704</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analysis of serum immune markers in seropositive and seronegative rheumatoid arthritis and in high-risk seropositive arthralgia patients.</pubmed_title><pmcid>PMC4870704</pmcid><pubmed_authors>Chalan P</pubmed_authors><pubmed_authors>van den Berg A</pubmed_authors><pubmed_authors>Brouwer E</pubmed_authors><pubmed_authors>Bijzet J</pubmed_authors><pubmed_authors>Kluiver J</pubmed_authors><pubmed_authors>Boots AM</pubmed_authors><pubmed_authors>Kroesen BJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of serum immune markers in seropositive and seronegative rheumatoid arthritis and in high-risk seropositive arthralgia patients.</name><description>Presence of autoantibodies precedes development of seropositive rheumatoid arthritis (SP RA) and seropositive arthralgia patients (SAP) are at risk of developing RA. The aims of the study are to identify additional serum immune markers discriminating between SP and seronegative (SN) RA, and markers identifying high-risk SAP. Sera from SAP (n = 27), SP RA (n = 22), SN RA (n = 11) and healthy controls (n = 20) were analyzed using the Human Cytokine 25-Plex Panel. Selected markers were validated in independent cohorts of SP RA (n = 35) and SN RA (n = 12) patients. Eleven of 27 SAP developed RA within 8 months (median follow-up time, range 1-32 months), and their baseline serum markers were compared to 16 non-progressing SAP. SAP and SP RA patients showed a marked overlap in their systemic imm</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 May</publication><modification>2025-04-04T09:37:12.234Z</modification><creation>2019-03-27T02:13:56Z</creation></dates><accession>S-EPMC4870704</accession><cross_references><pubmed>27189045</pubmed><doi>10.1038/srep26021</doi></cross_references></HashMap>