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        <datestamp>2026-09-24T05:33:08Z</datestamp>
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          <dc:title>Table 1_Low-density lipoprotein cholesterol modulates amyloid-related entorhinal vulnerability and episodic memory performance in older adults.docx</dc:title>
          <dc:creator>Minh Le Tran (16490953)</dc:creator>
          <dc:creator>Kahye Kim (12716858)</dc:creator>
          <dc:creator>Jaeuk U. Kim (12395383)</dc:creator>
          <dc:creator>Yu Yong Choi (9233111)</dc:creator>
          <dc:creator>JunHyeong Do (25102234)</dc:creator>
          <dc:creator>Kun Ho Lee (7465397)</dc:creator>
          <dc:creator>Ji-Woo Seok (5784686)</dc:creator>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>Alzheimer’s disease</dc:subject>
          <dc:subject>amyloid-beta</dc:subject>
          <dc:subject>entorhinal cortex</dc:subject>
          <dc:subject>episodic memory</dc:subject>
          <dc:subject>low-density lipoprotein cholesterol</dc:subject>
          <dc:subject>moderated mediation</dc:subject>
          <dc:description>Introduction&lt;p&gt;Cerebral amyloid-beta (Aβ) burden does not fully explain variation in Alzheimer’s disease (AD)-related brain structure and episodic memory. We examined whether circulating low-density lipoprotein cholesterol (LDL-C) modifies the cross-sectional statistical association between Aβ burden, the entorhinal cortex (EC) thickness and episodic memory performance.&lt;/p&gt;Methods&lt;p&gt;Cross-sectional data from 1,253 individuals in the Gwangju Alzheimer’s Disease and Related Dementias cohort (798 cognitively normal, 425 mild cognitive impairment, 30 AD dementia) were analyzed. Primary conditional-process models were adjusted for age, sex, education, body mass index, and HbA1c; clinical diagnosis was examined in sensitivity analyses. HC3 heteroskedasticity-consistent inference was used for the focal interaction, and indirect associations were estimated using 10,000 bootstrap resamples.&lt;/p&gt;Results&lt;p&gt;Greater Aβ burden was associated with lower EC thickness (β = −0.0863, p = 0.0012), and EC thickness was positively associated with episodic memory (β = 0.3809, p &lt; 0.001). The unconditional indirect statistical association was supported (β = −0.0329, 95% bias-corrected bootstrap CI [−0.0647, −0.0072]). LDL-C modified the Aβ–EC association (β = −0.0937, HC3 SE = 0.0332, 95% CI [−0.1589, −0.0285], p = 0.0049), although the incremental explanatory magnitude was small (ΔR&lt;sup&gt;2&lt;/sup&gt; = 0.0082). The conditional Aβ–EC association was unsupported at approximately 66 mg/dL LDL-C (β = 0.0263, p = 0.583), not statistically supported at approximately 100 mg/dL (β = −0.0639, p = 0.060), and negative at 138 mg/dL (β = −0.1648, p &lt; 0.001). The index of moderated indirect association was supported (β = −0.0357, 95% bias-corrected bootstrap CI [−0.0637, −0.0119]); conditional indirect associations were most clearly supported at higher LDL-C levels. A similar interaction was observed for non-HDL cholesterol, suggesting that the pattern may reflect a broader atherogenic lipid context.&lt;/p&gt;Conclusion&lt;p&gt;Circulating LDL-C was associated with modest heterogeneity in the cross-sectional Aβ–EC relationship, with more clearly negative conditional associations observed at higher LDL-C levels. Longitudinal studies are needed to determine the temporal and clinical relevance of these findings.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T05:33:08Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fnagi.2026.1933036.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Low-density_lipoprotein_cholesterol_modulates_amyloid-related_entorhinal_vulnerability_and_episodic_memory_performance_in_older_adults_docx/33979921</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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