<?xml version='1.0' encoding='utf-8'?>
<?xml-stylesheet type="text/xsl" href="/v2/static/oai2.xsl"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-10-06T14:38:38Z</responseDate>
  <request identifier="oai:figshare.com:article/34054002" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/34054002</identifier>
        <datestamp>2026-10-02T04:41:46Z</datestamp>
        <setSpec>category_393</setSpec>
        <setSpec>portal_316</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_10_2026</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Table 6_Associations of systemic inflammatory indices with rheumatoid arthritis and all-cause mortality: a NHANES study with independent hospital-based replication.csv</dc:title>
          <dc:creator>Lin Wang (11986)</dc:creator>
          <dc:creator>Hao Yu (157186)</dc:creator>
          <dc:creator>Yuanyuan Cao (701070)</dc:creator>
          <dc:creator>Li Yu (81651)</dc:creator>
          <dc:subject>Foetal Development and Medicine</dc:subject>
          <dc:subject>all-cause mortality</dc:subject>
          <dc:subject>CALLY</dc:subject>
          <dc:subject>inflammatory indices</dc:subject>
          <dc:subject>RAR</dc:subject>
          <dc:subject>rheumatoid arthritis</dc:subject>
          <dc:subject>systemic inflammation</dc:subject>
          <dc:description>Background&lt;p&gt;Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease associated with substantial morbidity and increased mortality. Although several composite inflammatory indices have been proposed as accessible biomarkers, their associations with RA and long-term prognosis remain incompletely understood.&lt;/p&gt;Methods&lt;p&gt;We analyzed 15,545 adults from five NHANES cycles (2001–2010), including 1,075 participants with self-reported RA. Survey-weighted multivariable logistic regression was used to assess associations between inflammatory indices and prevalent RA. Among participants with RA, survey-weighted Kaplan–Meier and Cox regression analyses were used to evaluate all-cause mortality. Restricted cubic spline analyses examined potential nonlinear associations. An independent retrospective hospital-based cohort was used to assess the directional consistency of key RA-related associations.&lt;/p&gt;Results&lt;p&gt;Among 15,545 participants, 1,075 had self-reported RA. In the fully adjusted models, participants in the highest RAR quartile had greater odds of prevalent self-reported RA than those in the lowest quartile (OR, 1.86; 95% CI, 1.33–2.60), whereas higher CALLY was inversely associated with RA (Q4 vs. Q1: OR, 0.58; 95% CI, 0.43–0.78); both associations remained significant after FDR correction. Among participants with self-reported RA, higher RAR was associated with a greater hazard of all-cause mortality (Q4 vs. Q1: HR, 2.48; 95% CI, 1.62–3.77), whereas higher CALLY was associated with a lower mortality hazard (Q4 vs. Q1: HR, 0.44; 95% CI, 0.31–0.61), with both associations remaining significant after FDR correction. Restricted cubic spline analyses suggested nonlinear associations for several inflammatory indices. In the independent hospital-based cohort, several key RA-related inflammatory indices showed directionally consistent associations, supporting the reproducibility of the principal RA-related findings.&lt;/p&gt;Conclusion&lt;p&gt;RAR and CALLY showed the most consistent associations with both prevalent RA and all-cause mortality. These accessible inflammatory indices may warrant further evaluation as markers of systemic inflammatory and nutritional status in RA, but prospective validation is needed before clinical application.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-02T04:41:46Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmed.2026.1968785.s004</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_6_Associations_of_systemic_inflammatory_indices_with_rheumatoid_arthritis_and_all-cause_mortality_a_NHANES_study_with_independent_hospital-based_replication_csv/34054002</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
