Frontiers in Neurology (Jun 2018)

Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?

  • Leonie Beyer,
  • Johanna Meyer-Wilmes,
  • Sonja Schönecker,
  • Jonas Schnabel,
  • Eva Brendel,
  • Catharina Prix,
  • Georg Nübling,
  • Marcus Unterrainer,
  • Nathalie L. Albert,
  • Oliver Pogarell,
  • Robert Perneczky,
  • Robert Perneczky,
  • Robert Perneczky,
  • Robert Perneczky,
  • Cihan Catak,
  • Katharina Bürger,
  • Katharina Bürger,
  • Peter Bartenstein,
  • Peter Bartenstein,
  • Kai Bötzel,
  • Johannes Levin,
  • Johannes Levin,
  • Axel Rominger,
  • Axel Rominger,
  • Axel Rominger,
  • Matthias Brendel,
  • Matthias Brendel

DOI
https://doi.org/10.3389/fneur.2018.00483
Journal volume & issue
Vol. 9

Abstract

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Background: F-18-fluordeoxyglucose positron emission tomography (FDG-PET) is widely used for discriminative diagnosis of tau-positive atypical parkinsonian syndromes (T+APS). This approach now stands to be augmented with more specific tau tracers. Therefore, we retrospectively analyzed a large clinical routine dataset of FDG-PET images for evaluation of the strengths and limitations of stand-alone FDG-PET.Methods: A total of 117 patients (age 68.4 ± 11.1 y) underwent an FDG-PET exam. Patients were followed clinically for a minimum of one year and their final clinical diagnosis was recorded. FDG-PET was rated visually (positive/negative) and categorized as high, moderate or low likelihood of T+APS and other neurodegenerative disorders. We then calculated positive and negative predictive values (PPV/NPV) of FDG-PET readings for the different subgroups relative to their final clinical diagnosis.Results: Suspected diagnoses were confirmed by clinical follow-up (≥1 y) for 62 out of 117 (53%) patients. PPV was excellent when FDG-PET indicated a high likelihood of T+APS in combination with low to moderate likelihood of another neurodegenerative disorder. PPV was distinctly lower when FDG-PET indicated only a moderate likelihood of T+APS or when there was deemed equal likelihood of other neurodegenerative disorder. NPV of FDG-PET with a low likelihood for T+APS was high.Conclusions: FDG-PET has high value in clinical routine evaluation of suspected T+APS, gaining satisfactory differential diagnosis in two thirds of the patients. One third of patients would potentially profit from further evaluation by more specific radioligands, with FDG-PET serving gatekeeper function for the more expensive methods.

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