Role and potential of 18F-fluorodeoxyglucose-positron emission tomography-computed tomography in large-vessel

Javier Collada-Carrasco1, Nieves Gómez-León1, Valentina Castillo-Morales2

  • 1Department of Radiology, Hospital Universitario de La Princesa, Autonomous University of Madrid, IIS-Princesa, Madrid, Spain.

Frontiers in Medicine
|August 22, 2024
PubMed

Insights

18F-fluorodeoxyglucose positron emission tomography-computed tomography (18F-FDG-PET-CT) aids in diagnosing and monitoring large-vessel vasculitis (LVV). This imaging technique visualizes vessel inflammation, assesses disease activity, and guides personalized treatment strategies for better patient outcomes.

Area of Science:

  • Vascular Medicine
  • Nuclear Medicine
  • Radiology

Background:

  • Large-vessel vasculitis (LVV) encompasses conditions like giant cell arteritis (GCA), polymyalgia rheumatica (PMR), and Takayasu's arteritis (TAK).
  • These diseases present diagnostic and management challenges due to varied clinical symptoms and potential severe complications.
  • Accurate diagnosis and monitoring are crucial for effective patient management.

Purpose of the Study:

  • To highlight the role of 18F-fluorodeoxyglucose positron emission tomography-computed tomography (18F-FDG-PET-CT) in diagnosing and managing LVV.
  • To explore the utility of 18F-FDG-PET-CT in assessing disease activity, extent, and treatment response.
  • To emphasize the value of 18F-FDG-PET-CT in guiding treatment decisions and improving patient outcomes.

Main Methods:

  • Utilizing 18F-FDG-PET-CT to visualize inflammation in the aorta and its major branches.
  • Assessing disease activity and extent through standardized uptake values (SUVs) and lesion distribution.
  • Correlating imaging findings with clinical presentation and treatment response.

Main Results:

  • 18F-FDG-PET-CT effectively visualizes vessel wall inflammation in LVV, aiding in diagnosis and subtype differentiation.
  • The imaging modality helps assess disease distribution, including extracranial involvement in GCA and PMR phenotypes.
  • Reductions in FDG uptake on PET-CT correlate with improved disease control and treatment response.

Conclusions:

  • 18F-FDG-PET-CT is a valuable tool for the diagnosis, monitoring, and management of large-vessel vasculitis.
  • It provides crucial insights into disease activity, extent, and response to therapy, facilitating personalized treatment strategies.
  • Future research should refine PET-CT techniques and explore novel imaging modalities like PET-MRI for enhanced diagnostic accuracy in LVV.

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