Targeted brain proteomics uncover multiple pathways to Alzheimer's dementia

Ann Neurol. 2018 Jul;84(1):78-88. doi: 10.1002/ana.25266. Epub 2018 Jul 3.

Abstract

Objective: Previous gene expression analysis identified a network of coexpressed genes that is associated with β-amyloid neuropathology and cognitive decline in older adults. The current work targeted influential genes in this network with quantitative proteomics to identify potential novel therapeutic targets.

Methods: Data came from 834 community-based older persons who were followed annually, died, and underwent brain autopsy. Uniform structured postmortem evaluations assessed the burden of β-amyloid and other common age-related neuropathologies. Selected reaction monitoring quantified cortical protein abundance of 12 genes prioritized from a molecular network of aging human brain that is implicated in Alzheimer's dementia. Regression and linear mixed models examined the protein associations with β-amyloid load and other neuropathological indices as well as cognitive decline over multiple years preceding death.

Results: Average age at death was 88.6 years. Overall, 349 participants (41.9%) had Alzheimer's dementia at death. A higher level of PLXNB1 abundance was associated with more β-amyloid load (p = 1.0 × 10-7 ) and higher PHFtau tangle density (p = 2.3 × 10-7 ), and the association of PLXNB1 with cognitive decline is mediated by these known Alzheimer's disease pathologies. On the other hand, higher IGFBP5, HSPB2, and AK4 and lower ITPK1 levels were associated with faster cognitive decline, and, unlike PLXNB1, these associations were not fully explained by common neuropathological indices, suggesting novel mechanisms leading to cognitive decline.

Interpretation: Using targeted proteomics, this work identified cortical proteins involved in Alzheimer's dementia and begins to dissect two different molecular pathways: one affecting β-amyloid deposition and another affecting resilience without a known pathological footprint. Ann Neurol 2018;83:78-88.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aged, 80 and over
  • Alzheimer Disease / complications
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / metabolism
  • Autopsy
  • Brain / metabolism*
  • Cognition Disorders / etiology
  • DNA-Binding Proteins
  • Female
  • HSP27 Heat-Shock Proteins / metabolism
  • Humans
  • Insulin-Like Growth Factor Binding Protein 5 / metabolism
  • Male
  • Nerve Tissue Proteins / metabolism
  • Neuropsychological Tests
  • Protein Interaction Maps
  • Proteome / genetics
  • Proteome / metabolism*
  • Proteomics / methods*
  • Receptors, Cell Surface / metabolism
  • Residence Characteristics

Substances

  • Amyloid beta-Peptides
  • DNA-Binding Proteins
  • HSP27 Heat-Shock Proteins
  • HSPB2 protein, human
  • IGFBP5 protein, human
  • Insulin-Like Growth Factor Binding Protein 5
  • Nerve Tissue Proteins
  • PLXNB1 protein, human
  • Proteome
  • Receptors, Cell Surface
  • TARDBP protein, human