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        <datestamp>2026-09-16T05:28:23Z</datestamp>
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          <dc:title>Data Sheet 1_Serum uric acid variability and short-term mortality in chronic kidney disease: a retrospective cohort study with independent replication in MIMIC-IV.docx</dc:title>
          <dc:creator>Fan Zhu (474830)</dc:creator>
          <dc:creator>Wenyuan Gan (16900548)</dc:creator>
          <dc:creator>Wenli Chen (452472)</dc:creator>
          <dc:creator>Xingruo Zeng (14995680)</dc:creator>
          <dc:subject>Clinical and Sports Nutrition</dc:subject>
          <dc:subject>biological variability</dc:subject>
          <dc:subject>chronic kidney disease</dc:subject>
          <dc:subject>electronic health records</dc:subject>
          <dc:subject>MIMIC-IV</dc:subject>
          <dc:subject>serum uric acid</dc:subject>
          <dc:subject>short-term mortality</dc:subject>
          <dc:description>Inroduction&lt;p&gt;Within-person variation in serum uric acid (SUA) may reflect clinical instability, but its association with outcomes in chronic kidney disease (CKD) is uncertain.&lt;/p&gt;Methods&lt;p&gt;We studied 10,556 adults with EHR-defined CKD and at least three SUA measurements during a 365-day baseline window across a nine-hospital consortium. Variability was quantified primarily by the coefficient of variation (CV); the primary outcome was all-cause mortality, and secondary outcomes were a composite kidney endpoint and major adverse cardiovascular events (MACE). Cox models adjusted for demographics, comorbidities, baseline laboratory values, mean SUA, measurement number and medication use. Reproducibility of the short-term mortality association was assessed in MIMIC-IV.&lt;/p&gt;Results&lt;p&gt;During a median follow-up of 0.62 years, 649 deaths, 676 kidney events and 3,172 first MACE occurred. Higher SUA CV was associated with mortality in the fully adjusted model (hazard ratio [HR] per 1-SD increase 1.24, 95% CI 1.15–1.32; highest versus lowest tertile 1.87, 95% CI 1.50–2.33), whereas adjusted associations with kidney events (HR 1.01, 95% CI 0.93–1.10) and MACE (HR 1.02, 95% CI 0.98–1.05) were null. Of all deaths, 495 (76.3%) occurred within 90 days. In a post-90-day landmark analysis of 6,784 participants with more than 90 days of follow-up, the mortality association was not observed (154 deaths; HR 1.02, 95% CI 0.86–1.21). Results were similar after daily aggregation of SUA measurements and additional adjustment for urate-lowering therapy, colchicine and sodium-glucose cotransporter-2 inhibitors. In MIMIC-IV (n = 5,350; 931 deaths within 90 days), the adjusted HR per 1-SD increase in CV was 1.32 (95% CI 1.26–1.38).&lt;/p&gt;Discussion&lt;p&gt;Greater SUA variability was associated with mortality during short follow-up; the concentration of deaths within 90 days and the null post-90-day landmark estimate suggest that the exposure may primarily mark near-term clinical deterioration rather than a causal or durable long-term prognostic mechanism.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-16T05:28:23Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fnut.2026.1919779.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Serum_uric_acid_variability_and_short-term_mortality_in_chronic_kidney_disease_a_retrospective_cohort_study_with_independent_replication_in_MIMIC-IV_docx/33828442</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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