<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Puechal X</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To investigate whether antineutrophil cytoplasm antibody (ANCA)-negative and myeloperoxidase (MPO)-ANCA-positive granulomatosis with polyangiitis (GPA) differ from proteinase-3 (PR3)-ANCA-positive GPA.&lt;h4>Methods&lt;/h4>Diagnostic characteristics and outcomes of newly diagnosed French Vasculitis Study Group Registry patients with ANCA-negative, MPO-ANCA-positive or PR3-ANCA-positive GPA satisfying American College of Rheumatology criteria and/or Chapel Hill Conference Consensus Nomenclature were compared.&lt;h4>Results&lt;/h4>Among 727 GPA, 62 (8.5%) were ANCA-negative, 119 (16.4%) MPO-ANCA-positive and 546 (75.1%) PR3-ANCA-positive. ANCA-negative patients had significantly (p&lt;0.05) more limited disease (17.7% vs 5.8%) and less kidney involvement (35.5% vs 58.9%) than those PR3-AN</pubmed_abstract><journal>RMD open</journal><pagination>e002160</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8928389</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative study of granulomatosis with polyangiitis subsets according to ANCA status: data from the French Vasculitis Study Group Registry.</pubmed_title><pmcid>PMC8928389</pmcid><pubmed_authors>de Moreuil C</pubmed_authors><pubmed_authors>Blanchard-Delaunay C</pubmed_authors><pubmed_authors>Puechal X</pubmed_authors><pubmed_authors>Hachulla E</pubmed_authors><pubmed_authors>Terrier B</pubmed_authors><pubmed_authors>Hamidou M</pubmed_authors><pubmed_authors>Ruivard M</pubmed_authors><pubmed_authors>Quemeneur T</pubmed_authors><pubmed_authors>Lifermann F</pubmed_authors><pubmed_authors>Cohen P</pubmed_authors><pubmed_authors>Le Quellec A</pubmed_authors><pubmed_authors>Khouatra C</pubmed_authors><pubmed_authors>Mouthon L</pubmed_authors><pubmed_authors>Pagnoux C</pubmed_authors><pubmed_authors>Guillevin L</pubmed_authors><pubmed_authors>Jourde-Chiche N</pubmed_authors><pubmed_authors>Bonnotte B</pubmed_authors><pubmed_authors>Maurier F</pubmed_authors><pubmed_authors>Viallard JF</pubmed_authors><pubmed_authors>French Vasculitis Study Group</pubmed_authors><pubmed_authors>Iudici M</pubmed_authors><pubmed_authors>Godmer P</pubmed_authors><pubmed_authors>Le Gallou T</pubmed_authors><pubmed_authors>Aumaitre O</pubmed_authors><pubmed_authors>Karras A</pubmed_authors><pubmed_authors>Aouba A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative study of granulomatosis with polyangiitis subsets according to ANCA status: data from the French Vasculitis Study Group Registry.</name><description>&lt;h4>Objective&lt;/h4>To investigate whether antineutrophil cytoplasm antibody (ANCA)-negative and myeloperoxidase (MPO)-ANCA-positive granulomatosis with polyangiitis (GPA) differ from proteinase-3 (PR3)-ANCA-positive GPA.&lt;h4>Methods&lt;/h4>Diagnostic characteristics and outcomes of newly diagnosed French Vasculitis Study Group Registry patients with ANCA-negative, MPO-ANCA-positive or PR3-ANCA-positive GPA satisfying American College of Rheumatology criteria and/or Chapel Hill Conference Consensus Nomenclature were compared.&lt;h4>Results&lt;/h4>Among 727 GPA, 62 (8.5%) were ANCA-negative, 119 (16.4%) MPO-ANCA-positive and 546 (75.1%) PR3-ANCA-positive. ANCA-negative patients had significantly (p&lt;0.05) more limited disease (17.7% vs 5.8%) and less kidney involvement (35.5% vs 58.9%) than those PR3-AN</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-06-07T03:22:26.133Z</modification><creation>2025-04-04T23:02:42.772Z</creation></dates><accession>S-EPMC8928389</accession><cross_references><pubmed>35296533</pubmed><doi>10.1136/rmdopen-2021-002160</doi></cross_references></HashMap>