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        <datestamp>2026-09-25T04:22:07Z</datestamp>
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          <dc:title>Supplementary file 1_Hidden metabolic obesity phenotypes and risk of incident type 2 diabetes among BMI-defined non-obese adults: a secondary analysis of the NAGALA cohort.pdf</dc:title>
          <dc:creator>Chenrong Cai (25106986)</dc:creator>
          <dc:creator>Yang Wang (5921)</dc:creator>
          <dc:subject>Cell Metabolism</dc:subject>
          <dc:subject>abdominal obesity</dc:subject>
          <dc:subject>body mass index</dc:subject>
          <dc:subject>cohort study</dc:subject>
          <dc:subject>fatty liver</dc:subject>
          <dc:subject>hidden metabolic obesity</dc:subject>
          <dc:subject>non-obese adults</dc:subject>
          <dc:subject>type 2 diabetes mellitus</dc:subject>
          <dc:description>Background&lt;p&gt;Body mass index (BMI) may fail to capture clinically relevant heterogeneity in adiposity-related diabetes risk, particularly among Asian adults who are not classified as obese. We investigated whether abdominal obesity and fatty liver identify distinct risks of incident type 2 diabetes mellitus (T2DM) among adults with BMI &lt;25 kg/m&lt;sup&gt;2&lt;/sup&gt;.&lt;/p&gt;Methods&lt;p&gt;This secondary analysis used data from the Japanese NAGALA cohort. A total of 12,940 adults without diabetes at baseline and with BMI &lt;25 kg/m&lt;sup&gt;2&lt;/sup&gt; were classified into four phenotypes: neither abdominal obesity nor fatty liver, isolated abdominal obesity, isolated fatty liver, and combined abdominal obesity and fatty liver. Cox proportional hazards models were used to estimate hazard ratios (HRs) for incident T2DM. We additionally assessed adiposity-component burden, multiplicative and additive interaction, sex-specific associations, multiple sensitivity analyses, and incremental 5-year predictive performance.&lt;/p&gt;Results&lt;p&gt;During 78,694.5 person-years of follow-up, 201 incident T2DM events occurred. Incidence rates were 1.70, 2.61, 8.20, and 21.37 per 1,000 person-years across the four phenotypes, respectively. In the fully adjusted model, isolated abdominal obesity was not significantly associated with T2DM (HR 1.47, 95% CI 0.66–3.31), whereas isolated fatty liver (HR 3.43, 95% CI 2.41–4.87) and combined abdominal obesity and fatty liver (HR 8.10, 95% CI 4.65–14.12) were strongly associated with higher risk. Risk increased progressively with the number of non-BMI adiposity components (P for trend &lt;0.001). Associations with fatty liver were observed in both sexes, with no clear evidence of effect modification by sex (P for interaction=0.176), and remained robust in sensitivity analyses, including restriction to BMI &lt;23 kg/m&lt;sup&gt;2&lt;/sup&gt;. Adding abdominal obesity, fatty liver, or the four-level phenotype to a comprehensive clinical model did not clearly improve 5-year predictive performance.&lt;/p&gt;Conclusions&lt;p&gt;Among BMI-defined non-obese adults, fatty liver—especially when accompanied by abdominal obesity—identified substantial heterogeneity in incident T2DM risk. These findings highlight the limitations of BMI alone for characterizing adiposity-related metabolic risk, while not establishing incremental predictive utility beyond established clinical risk factors.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-25T04:22:07Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fendo.2026.1959132.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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