<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim S</submitter><funding>research promoting grant from the AT&amp;amp;C in 2020</funding><funding>National Research Foundation of Korea</funding><pagination>258</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8949138</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(3)</volume><pubmed_abstract>The visceral adipose tissue (VAT) has been recognized as an endocrine organ, and VAT dysfunction could be a risk factor for Alzheimer's disease (AD). We aimed to evaluate the association of VAT metabolism with AD pathology. This cross-sectional study included 54 older subjects with cognitive impairment who underwent 2-deoxy-2-[fluorine-18]-fluoro-D-glucose (18F-FDG) torso positron emission tomography (PET) and 18F-florbetaben brain PET. 18F-FDG uptake in VAT on 18F-FDG PET images was used as a marker of VAT metabolism, and subjects were classified into high and low VAT metabolism groups. A voxel-based analysis revealed that the high VAT metabolism group exhibited a significantly higher cerebral amyloid-β (Aβ) burden than the low VAT metabolism group. In the volume-of-interest analysis, mul</pubmed_abstract><journal>Metabolites</journal><pubmed_title>Association between Visceral Adipose Tissue Metabolism and Alzheimer's Disease Pathology.</pubmed_title><pmcid>PMC8949138</pmcid><funding_grant_id>2020R1F1A1070405</funding_grant_id><funding_grant_id>2020</funding_grant_id><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Lee JS</pubmed_authors><pubmed_authors>Kim HW</pubmed_authors><pubmed_authors>Won KS</pubmed_authors><pubmed_authors>Yi HA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between Visceral Adipose Tissue Metabolism and Alzheimer's Disease Pathology.</name><description>The visceral adipose tissue (VAT) has been recognized as an endocrine organ, and VAT dysfunction could be a risk factor for Alzheimer's disease (AD). We aimed to evaluate the association of VAT metabolism with AD pathology. This cross-sectional study included 54 older subjects with cognitive impairment who underwent 2-deoxy-2-[fluorine-18]-fluoro-D-glucose (18F-FDG) torso positron emission tomography (PET) and 18F-florbetaben brain PET. 18F-FDG uptake in VAT on 18F-FDG PET images was used as a marker of VAT metabolism, and subjects were classified into high and low VAT metabolism groups. A voxel-based analysis revealed that the high VAT metabolism group exhibited a significantly higher cerebral amyloid-β (Aβ) burden than the low VAT metabolism group. In the volume-of-interest analysis, mul</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-19T21:44:53.958Z</modification><creation>2025-04-19T21:44:53.958Z</creation></dates><accession>S-EPMC8949138</accession><cross_references><pubmed>35323701</pubmed><doi>10.3390/metabo12030258</doi></cross_references></HashMap>