<?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>2026-10-14T13:09:59Z</responseDate>
  <request identifier="oai:figshare.com:article/33717508" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/33717508</identifier>
        <datestamp>2026-09-14T04:25:33Z</datestamp>
        <setSpec>category_393</setSpec>
        <setSpec>portal_316</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_09_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 1_Efficacy and safety of dupilumab in moderate-to-severe atopic dermatitis with stage 3–5 chronic kidney disease: a retrospective real-world study.docx</dc:title>
          <dc:creator>Jiali Wei (6062375)</dc:creator>
          <dc:creator>Yiqi Huang (1434637)</dc:creator>
          <dc:subject>Foetal Development and Medicine</dc:subject>
          <dc:subject>atopic dermatitis</dc:subject>
          <dc:subject>chronic kidney disease</dc:subject>
          <dc:subject>dupilumab</dc:subject>
          <dc:subject>efficacy</dc:subject>
          <dc:subject>safety</dc:subject>
          <dc:description>Aims&lt;p&gt;To evaluate dupilumab efficacy and safety in stage 3–5 chronic kidney disease (CKD) patients with moderate-to-severe atopic dermatitis (AD).&lt;/p&gt;Methods&lt;p&gt;This retrospective study included 29 such patients receiving dupilumab who completed 12 and 24 weeks of follow-up. Assessments included Eczema Area and Severity Index (EASI), Pruritus Numeric Rating Scale (NRS), Sleep NRS, Dermatology Life Quality Index (DLQI), and Clinical Frailty Scale (CFS), eosinophils, interleukin-10 (IL-10), regulatory T cell (Treg) proportions, and renal function [estimated glomerular filtration rate (eGFR), serum creatinine, and urine protein-to-creatinine ratio (UPCR)]. Adverse events were recorded.&lt;/p&gt;Results&lt;p&gt;At week 12, mean EASI score decreased from 34.94 ± 7.96 at baseline to 19.31 ± 6.09 (44.7% reduction), with 76.0% of patients achieving EASI-50. Pruritus NRS decreased from 7.72 ± 1.75 to 3.72 ± 1.75 (51.8% reduction), and 88.0% achieved a ≥ 4-point improvement. DLQI improved by 52.1%, and 100% of patients achieved a ≥ 4-point improvement. CFS score decreased by 17.5%. Eosinophil counts decreased by 25.0%, while IL-10 and Treg proportions increased by 49.9% and 50.8%, respectively. At week 24, EASI-50, EASI-75, and EASI-90 response rates were 100%, 76.9%, and 7.7%, respectively; 100% of patients achieved ≥4-point improvements in both pruritus NRS and DLQI. IL-10 and Treg continued to rise, and CFS score was significantly reduced from baseline (P = 0.001). Renal function parameters remained stable throughout the 24-week follow-up: mean eGFR showed a minimal decline from 37.93 ± 14.88 to 36.39 ± 14.77 mL/min/1.73 m&lt;sup&gt;2&lt;/sup&gt; at week 24 (P = 0.073), serum creatinine and UPCR also showed no significant changes (P = 0.130 and P = 0.069, respectively). Only two mild-to-moderate adverse events (injection-site reaction and conjunctivitis) occurred, both resolved with symptomatic management. No treatment discontinuation, death, or worsening of renal function was reported.&lt;/p&gt;Conclusion&lt;p&gt;Dupilumab effectively improves skin lesions, pruritus, sleep, quality of life, and frailty, while showing changes consistent with regulatory immune modulation in patients with stage 3–5 CKD and moderate-to-severe AD, with a favorable safety profile. Renal impairment alone should not be considered an absolute contraindication, although patients with advanced CKD require careful monitoring.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T04:25:33Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmed.2026.1906235.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Efficacy_and_safety_of_dupilumab_in_moderate-to-severe_atopic_dermatitis_with_stage_3_5_chronic_kidney_disease_a_retrospective_real-world_study_docx/33717508</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
