The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia

Ann Neurol. 1998 Jul;44(1):134-8. doi: 10.1002/ana.410440122.

Abstract

Frontotemporal dementia (FTD) is the most common early-onset non-Alzheimer's dementia (non-AD). Although the role of the epsilon4 allele of apolipoprotein E (ApoE) has been well established in AD, studies of ApoE allele distribution in patients with FTD have produced variable results. We studied 33 rigorously diagnosed FTD patients, including several who were pathologically confirmed, and compared the frequency of the epsilon4 allele in patients with FTD with the frequency in those with early-onset AD (EOAD), in those with late-onset AD (LOAD), and in non-demented elderly controls. The frequency of ApoE epsilon4 was 21% in patients with FTD, significantly less than the ApoE epsilon4 frequency in those patients with EOAD (38%) and those with LOAD (40%), but not significantly different from the ApoE epsilon4 frequency in elderly controls (13%).

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles*
  • Apolipoprotein E4
  • Apolipoproteins E / genetics*
  • Base Sequence
  • Dementia / genetics*
  • Female
  • Gene Frequency
  • Genetic Markers
  • Humans
  • Male
  • Middle Aged
  • Risk Factors

Substances

  • Apolipoprotein E4
  • Apolipoproteins E
  • Genetic Markers