Glucose metabolism of visceral adipose tissue measured by 18F-FDG PET/CT is related to the presence of colonic adenoma.

Medicine (Baltimore)

Department of Nuclear Medicine Health Promotion Center Department of Internal Medicine Department of Conservative Dentistry, College of Medicine, Ewha Womans University, Seoul, Republic of Korea.

Published: June 2017

AI Article Synopsis

  • The study explored the link between adipose tissue characteristics and colorectal adenoma (CRA), involving 212 participants who underwent PET/CT scans and colonoscopies.
  • Key findings showed that CRA presence was associated with older age, male sex, and higher measurements of body metrics like BMI and waist circumference, as well as increased visceral and total adipose tissue.
  • Lower glucose metabolism in visceral adipose tissue (indicated by lower SUV values) was found to be an independent predictor of CRA, suggesting that metabolic dysfunction in visceral fat may signify a higher risk for developing colorectal adenomas.

Article Abstract

This study investigated the relationships between the area and metabolic activity of adipose tissue and the presence of colorectal adenoma (CRA). Our institutional review board approved the study and waived informed consent. A total of 212 subjects who underwent fluorine 18 fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) and colonoscopy for routine health check-ups were enrolled. The volumetric parameters of areas of visceral (VATav), subcutaneous (SATav), and total adipose tissue (TATav) and calculated visceral-to-subcutaneous adipose tissue ratio (VSR) and visceral-to-total adipose tissue ratio (VAR) were considered. Metabolic parameters of standardized uptake value (SUV) of visceral (vcSUVmax, vcSUVmean), subcutaneous (scSUVmax, scSUVmean), and calculated visceral-to-subcutaneous adipose tissue ratio (VSRmax, VSRmean) were considered. Anthropometric data of height, weight, body mass index (BMI), waist circumference (WC), body fat mass (BFM), skeletal muscle mass (SMM), and diverse laboratory data were also considered as variables. Sixty-six subjects were placed in the CRA group and 146 subjects in the non-CRA group. The presence of CRA was significantly correlated with older age (P  =  .001), male sex (P  =  .041), higher BMI (P  =  .004), higher WC (P  =  .001), higher BFM (P  =  .024), higher VATav (P < .001), higher TATav (P  =  .004), higher VSR (P < .001), higher VAR (P < .001), lower vcSUVmax (P  =  .002), lower vcSUVmean (P < .001), and lower VSRmean (P  =  .002). On multiple regression analysis, vcSUVmax and vcSUVmean were independently associated with the presence of CRA (P  =  .009 and P  =  .045). Lower glucose metabolism of visceral adipose tissue was related to the presence of CRA. Our findings identify the value of visceral metabolic dysfunction as a potential surrogate marker of elevated risk for CRA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484200PMC
http://dx.doi.org/10.1097/MD.0000000000007156DOI Listing

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