<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mistegard CE</submitter><funding>Graduate School of HEALTH, Aarhus University</funding><funding>Aase and Ejnar Danielsen Foundation</funding><funding>The Danish National Research Foundation through the Center for Cellular Signal Patterns</funding><funding>Danish Rheumatism Association</funding><pagination>e004127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11328660</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To investigate lectin pathway proteins (LPPs) as biomarkers for axial spondyloarthritis (axSpA) in a cross-sectional cohort with a suspicion of axSpA, comprising newly diagnosed axSpA and chronic low back pain (cLBP) individuals.&lt;h4>Methods&lt;/h4>Serum samples from 515 participants within the OptiRef cohort, including 151 axSpA patients and 364 cLBP patients, were measured using immunoassays for LPPs (mannan-binding lectin (MBL), collectin liver-1 (CL-L1), M-ficolin, H-ficolin and L-ficolin, MBL-associated serine proteases (MASP)-1, -2 and -3, MBL-associated proteins (MAp19 and MAp44) and the complement activation product C3dg).&lt;h4>Results&lt;/h4>Serum levels of L-ficolin, MASP-2 and C3dg were elevated in axSpA patients, whereas levels of MASP-3 and CL-L1 were decreased, and </pubmed_abstract><journal>RMD open</journal><pubmed_title>Exploring complement biomarkers in suspected axial spondyloarthritis.</pubmed_title><pmcid>PMC11328660</pmcid><funding_grant_id>DNRF135</funding_grant_id><funding_grant_id>A6093 and A6462</funding_grant_id><pubmed_authors>Mistegard CE</pubmed_authors><pubmed_authors>Loft AG</pubmed_authors><pubmed_authors>Luders S</pubmed_authors><pubmed_authors>Proft F</pubmed_authors><pubmed_authors>Protopopov M</pubmed_authors><pubmed_authors>Troldborg A</pubmed_authors><pubmed_authors>Spiller L</pubmed_authors><pubmed_authors>Rios Rodriguez V</pubmed_authors><pubmed_authors>Muche B</pubmed_authors><pubmed_authors>Weber AK</pubmed_authors><pubmed_authors>Rademacher J</pubmed_authors><pubmed_authors>Thiel S</pubmed_authors><pubmed_authors>Sieper J</pubmed_authors><pubmed_authors>Poddubnyy D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploring complement biomarkers in suspected axial spondyloarthritis.</name><description>&lt;h4>Objectives&lt;/h4>To investigate lectin pathway proteins (LPPs) as biomarkers for axial spondyloarthritis (axSpA) in a cross-sectional cohort with a suspicion of axSpA, comprising newly diagnosed axSpA and chronic low back pain (cLBP) individuals.&lt;h4>Methods&lt;/h4>Serum samples from 515 participants within the OptiRef cohort, including 151 axSpA patients and 364 cLBP patients, were measured using immunoassays for LPPs (mannan-binding lectin (MBL), collectin liver-1 (CL-L1), M-ficolin, H-ficolin and L-ficolin, MBL-associated serine proteases (MASP)-1, -2 and -3, MBL-associated proteins (MAp19 and MAp44) and the complement activation product C3dg).&lt;h4>Results&lt;/h4>Serum levels of L-ficolin, MASP-2 and C3dg were elevated in axSpA patients, whereas levels of MASP-3 and CL-L1 were decreased, and </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-04-19T20:41:35.466Z</modification><creation>2025-04-19T20:41:35.466Z</creation></dates><accession>S-EPMC11328660</accession><cross_references><pubmed>38749532</pubmed><doi>10.1136/rmdopen-2024-004127</doi></cross_references></HashMap>