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Association between volume and glucose metabolism of abdominal adipose tissue in healthy population

Authors
Kwon, Hyun WooLee, Sang MiLee, Jeong WonOh, Jung-EunLee, Se-WhanKim, Shin Young
Issue Date
Sep-2017
Publisher
Elsevier BV
Keywords
Subcutaneous adipose tissue; Visceral fat; Glucose metabolism
Citation
Obesity Research and Clinical Practice, v.11, no.5, pp 133 - 143
Pages
11
Journal Title
Obesity Research and Clinical Practice
Volume
11
Number
5
Start Page
133
End Page
143
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/7270
DOI
10.1016/j.orcp.2016.12.007
ISSN
1871-403X
1878-0318
Abstract
Objective: We investigated the association of adipose tissue volume and metabolic activity with cardiometabolic risk factors. Methods: 232 healthy subjects (43.23 +/- 4.09 y) having F-18-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) results were included. Clinical information, anthropometry and laboratory results were obtained. Volume and metabolic activity of subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) was obtained from FDG PET/CT. Metabolic activity was presented as mean standardised uptake value (SUV). Adipose tissue parameters were compared with clinical and biochemical factors. Independent factors affecting adipose tissue volume were assessed. Results: Both SAT and VAT volume showed strong positive correlation with most of cardiometabolic risk factors. Among them, lipid profiles, insulin and C-reactive protein (CRP) had more significant relationship with SUV of SAT than that of VAT. On the contrary, glucose, glycated hemoglobin, and degree of fatty liver showed more significant correlation with SUV of VAT. BMI, age, sex and CRP were independent predictors of SAT volume. BMI, age, triglyceride, CRP and fatty liver were independent variables predicting VAT volume. Adding SUV of adipose tissue improved the model performance. Conclusion: This study demonstrated that metabolic activities of SAT and VAT were differently correlated with risk factors, suggesting different biologic mechanism for obesity. (C) 2017 Asia Oceania Association for the Study of Obesity. Published by Elsevier Ltd. All rights reserved.
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