<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Choi MY</submitter><funding>Novo Nordisk Foundation</funding><funding>Ministry for Health and Welfare, Republic of Korea</funding><funding>National Institute for Health Research Manchester Biomedical Research Centre</funding><funding>Arthritis Society</funding><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>Korea Healthcare</funding><funding>Canadian Institutes of Health Research</funding><funding>Canada Research Chairs</funding><funding>CIHR</funding><funding>Department of Education, Universities and Research of the Basque Government</funding><funding>LUPUS UK</funding><funding>Lupus Foundation of America</funding><funding>London Hospitals Biomedical Research Centre</funding><funding>National Institute for Health Research (NIHR)</funding><funding>NIAMS NIH HHS</funding><funding>Wellcome Trust</funding><funding>Gigtforeningen</funding><funding>Sandwell and West Birmingham Hospitals NHS Trust</funding><funding>Singer Family Fund for Lupus Research</funding><pagination>1143-1150</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10066935</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(8)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>A perception derived from cross-sectional studies of small systemic lupus erythematosus (SLE) cohorts is that there is a marked discrepancy between antinuclear antibody (ANA) assays, which impacts on clinicians' approach to diagnosis and follow-up. We compared three ANA assays in a longitudinal analysis of a large international incident SLE cohort retested regularly and followed for 5 years.&lt;h4>Methods&lt;/h4>Demographic, clinical and serological data was from 805 SLE patients at enrolment, year 3 and 5. Two HEp-2 indirect immunofluorescence assays (IFA1, IFA2), an ANA ELISA, and SLE-related autoantibodies were performed in one laboratory. Frequencies of positivity, titres or absorbance units (AU), and IFA patterns were compared using McNemar, Wilcoxon and kappa statistics,</pubmed_abstract><journal>Annals of the rheumatic diseases</journal><pubmed_title>Longitudinal analysis of ANA in the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort.</pubmed_title><pmcid>PMC10066935</pmcid><funding_grant_id>UL1 TR000150</funding_grant_id><funding_grant_id>A120404</funding_grant_id><funding_grant_id>Manchester Clinical Research Facility</funding_grant_id><funding_grant_id>AR069572</funding_grant_id><funding_grant_id>NF-SI-0512-10105</funding_grant_id><funding_grant_id>A1028</funding_grant_id><funding_grant_id>R01 AR046588</funding_grant_id><funding_grant_id>P60AR064464</funding_grant_id><funding_grant_id>RR00046</funding_grant_id><funding_grant_id>AR043727</funding_grant_id><funding_grant_id>R01 AR069572</funding_grant_id><funding_grant_id>Clinical Research Facility in Birmingham</funding_grant_id><funding_grant_id>UL1 RR025741</funding_grant_id><funding_grant_id>Systemic Autoimmune Rheumatic Diseases at Universi</funding_grant_id><funding_grant_id>A05990</funding_grant_id><funding_grant_id>MOP-88526</funding_grant_id><funding_grant_id>R01 AR043727</funding_grant_id><funding_grant_id>K24-AR-02318</funding_grant_id><funding_grant_id>Research Chair in Rheumatic Diseases at the Univer</funding_grant_id><funding_grant_id>NF-SI-0617-10075</funding_grant_id><funding_grant_id>1U54TR001353</funding_grant_id><funding_grant_id>P60 AR064464</funding_grant_id><funding_grant_id>UL-1RR-025741</funding_grant_id><funding_grant_id>K24 AR002138</funding_grant_id><funding_grant_id>K24 AR002213</funding_grant_id><funding_grant_id>K24 AR066109</funding_grant_id><funding_grant_id>P60 AR048098</funding_grant_id><funding_grant_id>AR046588</funding_grant_id><funding_grant_id>Gary S Gilkeson Career Development Award</funding_grant_id><funding_grant_id>Distinguished Senior Investigator of The Arthritis</funding_grant_id><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Wallace DJ</pubmed_authors><pubmed_authors>Kalunian K</pubmed_authors><pubmed_authors>Petri M</pubmed_authors><pubmed_authors>Choi MY</pubmed_authors><pubmed_authors>Dooley MA</pubmed_authors><pubmed_authors>Buyon JP</pubmed_authors><pubmed_authors>Clarke AE</pubmed_authors><pubmed_authors>Sanchez-Guerrero J</pubmed_authors><pubmed_authors>Manzi S</pubmed_authors><pubmed_authors>Jonsen A</pubmed_authors><pubmed_authors>Fortin PR</pubmed_authors><pubmed_authors>Fritzler MJ</pubmed_authors><pubmed_authors>Peschken C</pubmed_authors><pubmed_authors>Alarcon GS</pubmed_authors><pubmed_authors>Rahman A</pubmed_authors><pubmed_authors>Bernatsky S</pubmed_authors><pubmed_authors>Bruce IN</pubmed_authors><pubmed_authors>Costenbader KH</pubmed_authors><pubmed_authors>Ginzler EM</pubmed_authors><pubmed_authors>Ramsey-Goldman R</pubmed_authors><pubmed_authors>St-Pierre Y</pubmed_authors><pubmed_authors>Romero-Diaz J</pubmed_authors><pubmed_authors>Gladman DD</pubmed_authors><pubmed_authors>Merrill JT</pubmed_authors><pubmed_authors>Hanly J</pubmed_authors><pubmed_authors>Bae SC</pubmed_authors><pubmed_authors>Ruiz-Irastorza G</pubmed_authors><pubmed_authors>Askanase A</pubmed_authors><pubmed_authors>Aranow C</pubmed_authors><pubmed_authors>Urowitz M</pubmed_authors><pubmed_authors>Gordon C</pubmed_authors><pubmed_authors>Inanc M</pubmed_authors><pubmed_authors>Mackay M</pubmed_authors><pubmed_authors>van Vollenhoven RF</pubmed_authors><pubmed_authors>Isenberg D</pubmed_authors><pubmed_authors>Kamen DL</pubmed_authors><pubmed_authors>Jacobsen S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Longitudinal analysis of ANA in the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort.</name><description>&lt;h4>Objectives&lt;/h4>A perception derived from cross-sectional studies of small systemic lupus erythematosus (SLE) cohorts is that there is a marked discrepancy between antinuclear antibody (ANA) assays, which impacts on clinicians' approach to diagnosis and follow-up. We compared three ANA assays in a longitudinal analysis of a large international incident SLE cohort retested regularly and followed for 5 years.&lt;h4>Methods&lt;/h4>Demographic, clinical and serological data was from 805 SLE patients at enrolment, year 3 and 5. Two HEp-2 indirect immunofluorescence assays (IFA1, IFA2), an ANA ELISA, and SLE-related autoantibodies were performed in one laboratory. Frequencies of positivity, titres or absorbance units (AU), and IFA patterns were compared using McNemar, Wilcoxon and kappa statistics,</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-04T21:09:58.076Z</modification><creation>2025-04-04T21:09:58.076Z</creation></dates><accession>S-EPMC10066935</accession><cross_references><pubmed>35338033</pubmed><doi>10.1136/annrheumdis-2022-222168</doi></cross_references></HashMap>