Abstract

Association of blood pool (BP) and adipose tissue activity from F-18 fluorodeoxyglucose positron-emission tomography/computed tomography (FDG PET/CT) with the parameters of metabolic syndrome (MetS) and different MetS/obesity types were investigated. 245 subjects underwent FDG PET/CT scan for health check-ups were investigated retrospectively. Associations of BP (BP SUV: SUVmax, SUVmean), visceral (VAT SUV), and subcutaneous adipose tissue (SAT SUV) activity with parameters of MetS, body mass index (BMI), and lipid profiles were analyzed. MetS/obesity types were subdivided into metabolically healthy obese (MHO) and metabolically unhealthy obese (MUO). BP SUV was higher in subjects with MetS (t-test, P < 0.005), and was associated with MetS from multivariable binary logistic regression (OR 5.232 P = 0.010). BP SUV was statistically higher in MUO than in MHO (P < 0.05) along with blood pressure, triglycerides, and HDL-cholesterol. Multivariable binary logistic regression analysis showed MUO had higher blood pressure and BP SUV, while lower HDL-cholesterol relative to MHO after adjusting for triglycerides.

Highlights

  • Metabolic syndrome (MetS) is one of the most serious health conditions worldwide, which is associated with increased cardiocerebrovascular disease and all-cause ­mortality[1]

  • We investigated the metabolic activity of adipose tissue and blood pool using FDG positron emission tomography/computed tomography (PET/CT) with parameters related to metabolic syndrome and obesity status to evaluate the possible imaging biomarkers for MetS

  • Adipose tissue metabolic activities were correlated with blood pool activity; no adipose tissue metabolic activity was significantly different among different metabolic and obesity groups

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Summary

Introduction

Metabolic syndrome (MetS) is one of the most serious health conditions worldwide, which is associated with increased cardiocerebrovascular disease and all-cause ­mortality[1]. Due to the ability to represent the physiologic metabolic state of the entire body in vivo, there have been several attempts to use FDG PET/CT for non-tumor imaging biomarkers. The metabolic activity of organs, such as blood pool, liver, and spleen, has been investigated with several other diseases related to systemic inflammation or metabolic ­state[14,15]. Instead of being a reference organ, the blood pool activity itself could be the possible parameter reflecting the metabolic status. We investigated the metabolic activity of adipose tissue and blood pool using FDG PET/CT with parameters related to metabolic syndrome and obesity status to evaluate the possible imaging biomarkers for MetS

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