The Amyloid Cascade Hypothesis in Alzheimer's Disease: It's Time to Change Our Mind

Curr Neuropharmacol. 2017;15(6):926-935. doi: 10.2174/1570159X15666170116143743.

Abstract

Since its discovery in 1984, the beta amyloid peptide has treaded the boards of neurosciences as the star molecule in Alzheimer's disease pathogenesis. In the last decade, however, this vision has been challenged by evidence-based medicine showing the almost complete failure of clinical trials that experimented anti-amyloid therapies with great hopes. Moreover, data have accumulated which clearly indicate that this small peptide plays a key role in the physiological processes of memory formation. In the present review, we will discuss the different aspects of the amyloid cascade hypothesis, highlighting its pros and cons, and we will analyse the results of the therapeutic approaches attempted to date that should change the direction of Alzheimer's disease research in the future.

Keywords: Alzheimer's disease; LTP; anti-amyloid therapy; beta amyloid; clinical trials; memory.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Humans

Substances

  • Amyloid beta-Peptides