Breakpoint sequence analysis of an AβPP locus duplication associated with autosomal dominant Alzheimer's disease and severe cerebral amyloid angiopathy

J Alzheimers Dis. 2012;28(2):303-8. doi: 10.3233/JAD-2011-110911.

Abstract

AβPP locus duplications have been recently identified in early-onset Alzheimer's disease. We describe a patient who initiated memory problems and behavioral disturbances at 57 years, with a progressive cognitive decline, who died at the age of 68 years with dementia. Neuropathological examination revealed a temporobasal hemorrhage, extensive Alzheimer-type pathology, and severe cerebral amyloid angiopathy. We observed a chromosomal 21 region duplication spanning 0.59 Mb, which comprised JAM2, ATP5J, GABPA, and AβPP genes. We propose a replication based mutational mechanism (single Fork-Stalling and Template-Switching) or a recombination based one (non-homologous end-joining repair) for the AβPP locus duplication in this case.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / complications
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology
  • Amyloid beta-Protein Precursor / genetics*
  • Brain / pathology
  • Cerebral Amyloid Angiopathy / complications
  • Cerebral Amyloid Angiopathy / genetics*
  • Cerebral Amyloid Angiopathy / pathology
  • Cerebral Hemorrhage / complications
  • Cerebral Hemorrhage / genetics
  • Cerebral Hemorrhage / pathology
  • Genetic Testing
  • Humans
  • Male
  • Middle Aged
  • Nerve Tissue Proteins / metabolism
  • Point Mutation / genetics*
  • Spain
  • tau Proteins / metabolism

Substances

  • Amyloid beta-Protein Precursor
  • Nerve Tissue Proteins
  • tau Proteins