Predicting long-term clinical stability in amyloid-positive subjects by FDG-PET

Ann Clin Transl Neurol. 2019 May 24;6(6):1113-1120. doi: 10.1002/acn3.782. eCollection 2019 Jun.

Abstract

Imaging biomarkers can be used to screen participants for Alzheimer's disease clinical trials. To test the predictive values in clinical progression of neuropathology change (amyloid-PET) or brain metabolism as neurodegeneration biomarker ([18F]FDG-PET), we evaluated data from N = 268 healthy controls and N = 519 mild cognitive impairment subjects. Despite being a significant risk factor, amyloid positivity was not associated with clinical progression in the majority (≥60%) of subjects. Notably, a negative [18F]FDG-PET scan at baseline strongly predicted clinical stability with high negative predictive values (>0.80) for both groups. We suggest [18F]FDG-PET brain metabolism or other neurodegeneration measures should be coupled to amyloid-PET to exclude clinically stable individuals from clinical trials.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / diagnostic imaging*
  • Amyloid beta-Peptides / metabolism
  • Biomarkers / metabolism*
  • Brain
  • Clinical Trials as Topic
  • Cognitive Dysfunction / diagnostic imaging*
  • Dementia / diagnosis*
  • Disease Progression
  • Female
  • Fluorodeoxyglucose F18 / metabolism*
  • Healthy Volunteers
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Positron-Emission Tomography / methods*

Substances

  • Amyloid beta-Peptides
  • Biomarkers
  • Fluorodeoxyglucose F18