Progression of regional neuropathology in Alzheimer disease and normal elderly: findings from the Nun study

Alzheimer Dis Assoc Disord. 1999 Oct-Dec;13(4):226-31. doi: 10.1097/00002093-199910000-00009.

Abstract

Although diffuse plaques in the neocortex may represent an early stage in the evolution of neuritic plaques, plaques in the striatum and cerebellum retain their predominantly diffuse nature in Alzheimer disease (AD), regardless of disease duration. We had the opportunity to explore the progression of these regional features by using autopsy brain specimens from 15 cognitively normal and five AD subjects, all Catholic sisters enrolled in the Nun Study, a longitudinal study on aging and AD. Neuropathologic changes were assessed in the temporal cortex, striatum, and cerebellum without knowledge of clinical status. We found diffuse plaques in the striatum in six (40%) and cerebellar plaques in none of the brains from the non-demented subjects. Striatal plaques were present in all five and cerebellar plaques in four of the five AD cases. In the 20 cases overall, the presence of striatal plaques generally paralleled the occurrence of neuritic plaques in neocortex and correlated with lower scores on several neuropsychologic tests assessing memory. Our findings suggest that striatal diffuse plaques occur relatively early in the progression of AD pathology and coincide with neocortical pathology and cognitive changes. Thus, it is unlikely that temporal factors alone account for regional differences in progression of AD neuropathology.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Aging / pathology*
  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / metabolism*
  • Apolipoproteins E / genetics
  • Cerebellum / pathology*
  • Clergy
  • Corpus Striatum / pathology*
  • Female
  • Humans
  • Longitudinal Studies
  • Plaque, Amyloid / pathology*
  • Psychological Tests
  • Temporal Lobe / pathology

Substances

  • Amyloid beta-Peptides
  • Apolipoproteins E