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        <identifier>oai:figshare.com:article/34031373</identifier>
        <datestamp>2026-09-30T10:52:15Z</datestamp>
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          <dc:title>Supplemental Material for: Detecting Early Liver Fibrosis in Obesity: A Head-to-Head Comparison of Five Clinical Scores in Metabolic Dysfunction-Associated Steatotic Liver Disease</dc:title>
          <dc:creator>figshare admin karger (2628495)</dc:creator>
          <dc:creator>Giovani Schulte Farina (25143205)</dc:creator>
          <dc:creator>Bárbara Brambilla (10446051)</dc:creator>
          <dc:creator>Laura Kalil Nader Lazzaretti (25143209)</dc:creator>
          <dc:creator>Emanuelle Mendonça Pandolfo (25143212)</dc:creator>
          <dc:creator>Carlos Henrique Dal Bem Fistarol (25143216)</dc:creator>
          <dc:creator>Stéfano Matheus Schio Kuiava (25143219)</dc:creator>
          <dc:creator>Ana Maria Graciolli (25143220)</dc:creator>
          <dc:creator>Henrique Prataviera Giovanardi (25143223)</dc:creator>
          <dc:creator>Augusto Cardoso Sgarioni (25143229)</dc:creator>
          <dc:creator>Aline Caldart Tregnago (25143230)</dc:creator>
          <dc:creator>Floriano Rodrigues Riva Netod (25143231)</dc:creator>
          <dc:creator>Cassiano da Silva Scholze (25143243)</dc:creator>
          <dc:creator>Daniel Cecconi Agostini (25143245)</dc:creator>
          <dc:creator>Bruno Schmidt Dellamea (10446054)</dc:creator>
          <dc:creator>Lessandra Michelin Rodriguez Lins (25143250)</dc:creator>
          <dc:creator>Jonathan Soldera (10445862)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Introduction: Obesity is a major driver of metabolic dysfunction-associated steatotic liver disease (MASLD) and liver fibrosis, creating an urgent need for accurate, non-invasive tools to identify fibrosis in this high-risk population. We compared five clinical fibrosis scores (FIB-4, NFS, APRI, BARD, Hepamet) for detecting any fibrosis (F1–F4) in obese individuals at risk of MASLD and to assess whether metabolic syndrome (MetS) modifies score performance.&lt;/p&gt;&lt;p dir="ltr"&gt;Methods: We performed a cross-sectional study of 95 individuals undergoing bariatric surgery with intraoperative liver biopsy as reference. FIB-4, NFS, APRI, BARD, and Hepamet were calculated using pre-operative clinical and laboratory data. Fibrosis was staged by NASH CRN criteria. Diagnostic performance was evaluated using AUROC analysis and diagnostic measures with published and optimized (Youden index) cut-offs. The interaction between MetS and score performance was tested using logistic regression.&lt;/p&gt;&lt;p dir="ltr"&gt;Results: Fibrosis was present in 10.5% of participants. Using published cut-offs, FIB-4 (AUROC 0.752) and Hepamet (AUROC 0.746) showed fair discrimination, while NFS and APRI performed poorly and BARD showed no meaningful discrimination. Optimized cut-offs improved performance of FIB-4 (AUROC 0.789) and Hepamet (AUROC 0.781), both yielding high negative predictive values (&gt;95%). BARD remained suboptimal. MetS did not significantly modify the association between any score and fibrosis.&lt;/p&gt;&lt;p dir="ltr"&gt;Conclusions: In obese patients at risk of MASLD, FIB-4 and Hepamet provided the most reliable detection of biopsy-proven fibrosis, including early disease. Population-specific cut-offs improved accuracy, while MetS did not affect score performance. These findings support FIB-4 and Hepamet as practical tools for early fibrosis risk stratification in obese MASLD.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-30T10:52:15Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34031373.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplemental_Material_for_Detecting_Early_Liver_Fibrosis_in_Obesity_A_Head-to-Head_Comparison_of_Five_Clinical_Scores_in_Metabolic_Dysfunction-Associated_Steatotic_Liver_Disease/34031373</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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