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Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.

Neurobiology of aging | 2011

Many elderly individuals remain dementia-free throughout their life. However, some of these individuals exhibit Alzheimer disease neuropathology on autopsy, evidenced by neurofibrillary tangles (NFTs) in AD-specific brain regions. We conducted a genome-wide association study to identify genetic mechanisms that distinguish non-demented elderly with a heavy NFT burden from those with a low NFT burden. The study included 299 non-demented subjects with autopsy (185 subjects with low and 114 with high NFT levels). Both a genotype test, using logistic regression, and an allele test provided consistent evidence that variants in the RELN gene are associated with neuropathology in the context of cognitive health. Immunohistochemical data for reelin expression in AD-related brain regions added support for these findings. Reelin signaling pathways modulate phosphorylation of tau, the major component of NFTs, either directly or through β-amyloid pathways that influence tau phosphorylation. Our findings suggest that up-regulation of reelin may be a compensatory response to tau-related or beta-amyloid stress associated with AD even prior to the onset of dementia.

Pubmed ID: 20452100 RIS Download

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: P50-AG08671
  • Agency: NIA NIH HHS, United States
    Id: P50 AG008671
  • Agency: NIA NIH HHS, United States
    Id: P50 AG005131
  • Agency: NIA NIH HHS, United States
    Id: P30-AG008017
  • Agency: NIA NIH HHS, United States
    Id: R01-AG17917
  • Agency: NIA NIH HHS, United States
    Id: P30 AG010161
  • Agency: NIA NIH HHS, United States
    Id: P50-AG05681
  • Agency: NIA NIH HHS, United States
    Id: U01-AG016976
  • Agency: NIA NIH HHS, United States
    Id: P30 AG010129
  • Agency: NIA NIH HHS, United States
    Id: P30 AG028383
  • Agency: NIA NIH HHS, United States
    Id: P50-AG05131
  • Agency: NIA NIH HHS, United States
    Id: R01-AG026916
  • Agency: NIA NIH HHS, United States
    Id: P01-AG03991
  • Agency: NIA NIH HHS, United States
    Id: P30 AG008017-209005
  • Agency: NIA NIH HHS, United States
    Id: P30 AG028377
  • Agency: NIA NIH HHS, United States
    Id: P50 AG016574
  • Agency: NIA NIH HHS, United States
    Id: P50 AG005146
  • Agency: NIA NIH HHS, United States
    Id: P50-AG005146
  • Agency: NIA NIH HHS, United States
    Id: P30-AG10161
  • Agency: NIA NIH HHS, United States
    Id: U01 AG016976
  • Agency: NIA NIH HHS, United States
    Id: P01 AG003991
  • Agency: NIA NIH HHS, United States
    Id: P50 AG005681
  • Agency: NIA NIH HHS, United States
    Id: R01 AG026916-04
  • Agency: NIA NIH HHS, United States
    Id: R01 AG017917
  • Agency: NIA NIH HHS, United States
    Id: P50-AG16574
  • Agency: NIA NIH HHS, United States
    Id: P30-AG028377
  • Agency: NIA NIH HHS, United States
    Id: P30 AG008017
  • Agency: NIA NIH HHS, United States
    Id: P30-AG10129
  • Agency: NIA NIH HHS, United States
    Id: P30-AG028383
  • Agency: NIA NIH HHS, United States
    Id: R01 AG026916
  • Agency: NIA NIH HHS, United States
    Id: U01-AG06786
  • Agency: NIA NIH HHS, United States
    Id: U01 AG006786
  • Agency: NIA NIH HHS, United States
    Id: R01 AG015819

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SyStat (tool)

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A commercial software tool for statistical analysis.

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PLINK (tool)

RRID:SCR_001757

Open source whole genome association analysis toolset, designed to perform range of basic, large scale analyses in computationally efficient manner. Used for analysis of genotype/phenotype data. Through integration with gPLINK and Haploview, there is some support for subsequent visualization, annotation and storage of results. PLINK 1.9 is improved and second generation of the software.

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