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        <datestamp>2026-09-24T04:30:19Z</datestamp>
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          <dc:title>Table 1_Development and validation of a predictive model for rapid renal function decline in early IgA nephropathy: a multicenter retrospective study.docx</dc:title>
          <dc:creator>Junan Zhou (10233030)</dc:creator>
          <dc:creator>Yang Liu (4829)</dc:creator>
          <dc:creator>Lixia Huo (9330024)</dc:creator>
          <dc:creator>Xu Wu (318848)</dc:creator>
          <dc:creator>Zhelun Zhou (20926499)</dc:creator>
          <dc:creator>Haodong Liu (1539514)</dc:creator>
          <dc:creator>Rong Wu (152554)</dc:creator>
          <dc:creator>Jiaai Zhang (20926502)</dc:creator>
          <dc:creator>Yiqing Yu (19229362)</dc:creator>
          <dc:creator>Deyong Fan (25101721)</dc:creator>
          <dc:creator>Xiaoyi Wang (90589)</dc:creator>
          <dc:subject>Foetal Development and Medicine</dc:subject>
          <dc:subject>IgA nephropathy</dc:subject>
          <dc:subject>lambda light chain</dc:subject>
          <dc:subject>Oxford C score</dc:subject>
          <dc:subject>prediction model</dc:subject>
          <dc:subject>rapid renal function decline</dc:subject>
          <dc:description>&lt;p&gt;Immunoglobulin A nephropathy (IgAN) is a heterogeneous disease, and early identification of patients at high risk of rapid renal deterioration remains challenging. In this multicenter retrospective study, 483 patients with biopsy-proven IgAN at chronic kidney disease stages 1–3 were enrolled and randomly assigned to a training cohort (n = 338) and an internal validation cohort (n = 145). Rapid renal function decline was defined as a decline of at least 25% in estimated glomerular filtration rate or progression to ESRD, analyzed as a time-to-event outcome from renal biopsy (the 1-year risk was the principal metric reported). Independent predictors were identified using Cox proportional hazards regression, and a nomogram was developed and internally validated. In the training cohort, 83 patients (24.6%) reached the endpoint during follow-up (median time to event 13.6 months). Multivariable analysis showed that renal tissue Lambda light chain deposition, higher systolic blood pressure, serum chloride, blood urea nitrogen, and Oxford C score were independent risk factors, whereas higher serum complement C3 and potassium were protective factors. The nomogram showed good discrimination, with a 1-year time-dependent area under the receiver operating characteristic curve (AUC) of 0.86 (95% CI: 0.81–0.92) in the training cohort and 0.80 (95% CI: 0.69–0.91) in the validation cohort. SHAP analysis identified Lambda light chain deposition as the most influential predictor. In conclusion, we developed and internally validated a nomogram integrating clinicopathological variables to predict rapid renal function decline in early-stage IgAN, which may facilitate early risk stratification and individualized management.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T04:30:19Z</dc:date>
          <dc:type>Dataset</dc:type>
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          <dc:identifier>10.3389/fmed.2026.1857665.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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