Beyond amyloid: getting real about nonamyloid targets in Alzheimer's disease

Alzheimers Dement. 2013 Jul;9(4):452-458.e1. doi: 10.1016/j.jalz.2013.01.017.

Abstract

For decades, researchers have focused primarily on a pathway initiated by amyloid beta aggregation, amyloid deposition, and accumulation in the brain as the key mechanism underlying the disease and the most important treatment target. However, evidence increasingly suggests that amyloid is deposited early during the course of disease, even prior to the onset of clinical symptoms. Thus, targeting amyloid in patients with mild to moderate Alzheimer's disease (AD), as past failed clinical trials have done, may be insufficient to halt further disease progression. Scientists are investigating other molecular and cellular pathways and processes that contribute to AD pathogenesis. Thus, the Alzheimer's Association's Research Roundtable convened a meeting in April 2012 to move beyond amyloid and explore AD as a complex multifactorial disease, with the goal of using a more inclusive perspective to identify novel treatment strategies.

Publication types

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

MeSH terms

  • Aging
  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / drug therapy*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Autophagy / drug effects
  • Biomarkers
  • Brain / metabolism
  • Cell Cycle / drug effects
  • Cooperative Behavior
  • Diabetes Mellitus, Type 2 / complications
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Humans
  • Inflammation
  • Insulin Resistance
  • Lysosomes / drug effects
  • Lysosomes / physiology
  • Mice
  • Mice, Transgenic
  • Mitochondria / drug effects
  • Mitochondria / pathology
  • Models, Neurological
  • Molecular Targeted Therapy*
  • Neuroimaging
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / pathology
  • Nootropic Agents / pharmacology
  • Nootropic Agents / therapeutic use*
  • Public-Private Sector Partnerships
  • Resource Allocation
  • tau Proteins / drug effects
  • tau Proteins / physiology

Substances

  • Amyloid beta-Peptides
  • Biomarkers
  • MAPT protein, human
  • Nootropic Agents
  • tau Proteins