Development and validation of a novel dementia of Alzheimer's type (DAT) score based on metabolism FDG-PET imaging

Neuroimage Clin. 2018 Mar 10:18:802-813. doi: 10.1016/j.nicl.2018.03.007. eCollection 2018.

Abstract

Fluorodeoxyglucose positron emission tomography (FDG-PET) imaging based 3D topographic brain glucose metabolism patterns from normal controls (NC) and individuals with dementia of Alzheimer's type (DAT) are used to train a novel multi-scale ensemble classification model. This ensemble model outputs a FDG-PET DAT score (FPDS) between 0 and 1 denoting the probability of a subject to be clinically diagnosed with DAT based on their metabolism profile. A novel 7 group image stratification scheme is devised that groups images not only based on their associated clinical diagnosis but also on past and future trajectories of the clinical diagnoses, yielding a more continuous representation of the different stages of DAT spectrum that mimics a real-world clinical setting. The potential for using FPDS as a DAT biomarker was validated on a large number of FDG-PET images (N=2984) obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database taken across the proposed stratification, and a good classification AUC (area under the curve) of 0.78 was achieved in distinguishing between images belonging to subjects on a DAT trajectory and those images taken from subjects not progressing to a DAT diagnosis. Further, the FPDS biomarker achieved state-of-the-art performance on the mild cognitive impairment (MCI) to DAT conversion prediction task with an AUC of 0.81, 0.80, 0.77 for the 2, 3, 5 years to conversion windows respectively.

Keywords: Dementia of Alzheimer's type (DAT); FDG-PET; Glucose metabolism; Multi-scale ensemble classifier.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / diagnosis*
  • Biomarkers / metabolism
  • Brain / diagnostic imaging*
  • Brain / metabolism
  • Cognitive Dysfunction / diagnosis*
  • Disease Progression
  • Humans
  • Neuroimaging / methods
  • Positron-Emission Tomography* / methods
  • Radiopharmaceuticals / metabolism

Substances

  • Biomarkers
  • Radiopharmaceuticals