High 18F-FDG uptake in PMAH correlated with normal expression of Glut1, HK1, HK2, and HK3

Acta Radiol. 2016 Mar;57(3):370-7. doi: 10.1177/0284185115575195. Epub 2015 Mar 11.

Abstract

Background: Primary macronodular adrenal hyperplasia (PMAH) is a rare cause of Cushing's syndrome, characterized by functioning adrenal macronodules and variable cortisol production. Recently, we demonstrated a high 18F-FDG uptake in PMAH, an unexpected finding for a benign disorder.

Purpose: To investigate whether there is a correlation between 18F-FDG high uptake and the expression levels of the glycolytic pathway components GLUT1, HK1, HK2, and HK3 in PMAH.

Material and methods: We selected 12 patients undergoing surgery for PMAH who had preoperatively undergone 18F-FDG PET/CT. mRNA and protein expression of the selected genes were evaluated in the adrenal nodules from patients who underwent surgery through quantitative RT-PCR and by immunohistochemistry, respectively.

Results: SUVmax in PMAH was in the range of 3.3-8.9 and the adrenal size was in the range of 3.5-15 cm. A strong correlation between 18F-FDG uptake and largest adrenal diameter was observed in patients with PMAH. However, no correlation between 18F-FDG uptake and GLUT1, HK1, HK2, HK3 mRNA, and protein expression was observed.

Conclusion: High 18F-FDG uptake is observed in the majority of PMAH cases. However, 18F-FDG uptake in PMAH is independent of the expression levels of GLUT1, HK1, HK2, and HK3. Further investigation is required to elucidate the molecular mechanisms underlying increased 18F-FDG uptake in PMAH.

Keywords: 18F-FDG; Cushing’s syndrome; PET; Primary macronodular adrenal hyperplasia; adrenal; adults; hyperplasia; monoclonal antibodies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Glands / diagnostic imaging
  • Adrenal Glands / metabolism
  • Cushing Syndrome / genetics*
  • Cushing Syndrome / metabolism
  • Fluorodeoxyglucose F18 / pharmacokinetics*
  • Gene Expression / genetics*
  • Glucose Transporter Type 1 / genetics*
  • Glucose Transporter Type 1 / metabolism
  • Hexokinase / genetics*
  • Hexokinase / metabolism
  • Humans
  • Multimodal Imaging
  • Positron-Emission Tomography
  • Radiopharmaceuticals / pharmacokinetics
  • Real-Time Polymerase Chain Reaction
  • Tomography, X-Ray Computed

Substances

  • Glucose Transporter Type 1
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • HK1 protein, human
  • Hexokinase