Amyloid-first and neurodegeneration-first profiles characterize incident amyloid PET positivity

Neurology. 2013 Nov 12;81(20):1732-40. doi: 10.1212/01.wnl.0000435556.21319.e4. Epub 2013 Oct 16.

Abstract

Objective: To estimate the incidence of and to characterize cognitive and imaging findings associated with incident amyloid PET positivity.

Methods: Cognitively normal (CN) participants in the Mayo Clinic Study of Aging who had 2 or more serial imaging assessments, which included amyloid PET, FDG-PET, and MRI at each time point, were eligible for analysis (n = 207). Twelve subjects with Alzheimer disease dementia were included for comparison.

Results: Of the 123 CN participants who were amyloid-negative at baseline, 26 met criteria for incident amyloid PET positivity. Compared to the 69 subjects who remained stable amyloid-negative, on average these 26 did not differ on any imaging, demographic, or cognitive variables except amyloid PET (by definition) and task-free functional connectivity, which at baseline was greater in the incident amyloid-positive group. Eleven of the 26 incident amyloid-positive subjects had abnormal hippocampal volume, FDG-PET, or both at baseline.

Conclusions: The incidence of amyloid PET positivity is approximately 13% per year among CN participants over age 70 sampled from a population-based cohort. In 15/26 (58%), incident amyloid positivity occurred prior to abnormalities in FDG-PET and hippocampal volume. However, 11/26 (42%) incident amyloid-positive subjects had evidence of neurodegeneration prior to incident amyloid positivity. These 11 could be subjects with combinations of preexisting non-Alzheimer pathophysiologies and tau-mediated neurodegeneration who newly entered the amyloid pathway. Our findings suggest that both "amyloid-first" and "neurodegeneration-first" biomarker profile pathways to preclinical AD exist.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / diagnostic imaging
  • Amyloid / metabolism*
  • Brain / blood supply
  • Brain / diagnostic imaging
  • Brain / metabolism
  • Cognition Disorders / etiology
  • Female
  • Fluorodeoxyglucose F18
  • Follow-Up Studies
  • Humans
  • Image Processing, Computer-Assisted
  • Incidence
  • Magnetic Resonance Imaging
  • Male
  • Neurodegenerative Diseases / complications
  • Neurodegenerative Diseases / diagnostic imaging*
  • Neurodegenerative Diseases / metabolism*
  • Oxygen
  • Positron-Emission Tomography*

Substances

  • Amyloid
  • Fluorodeoxyglucose F18
  • Oxygen