TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease

Neurobiol Aging. 2011 Dec;32(12):2328.e1-9. doi: 10.1016/j.neurobiolaging.2011.06.016. Epub 2011 Aug 5.

Abstract

Apolipoprotein E (APOE) ε4 alleles increase the risk for late-onset Alzheimer disease (LOAD) and decrease the age of onset. Recently, sequencing the APOE region in a small sample of LOAD subjects identified a variable length poly-T repeat sequence in the nearby gene, TOMM40, which may affect age of onset. We genotyped the TOMM40 poly-T repeat using a novel statistical approach to refine the identification of allele length in 892 LOAD subjects and evaluated its effects on age of onset. Because psychosis in LOAD is a heritable phenotype which has shown conflicting associations with APOE genotype, we also evaluated the association of poly-T repeat length with psychosis. Poly-T repeat lengths had a trimodal distribution which differed between APOE genotype groups. After accounting for APOE ε4 there was no association of poly-T repeat length with age of onset. Neither APOE ε4 nor poly-T repeat length was associated with psychosis. Our findings do not support the association of poly-T repeat length with age of onset in LOAD. The clinical implications of this repeat length polymorphism remain to be elucidated.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / epidemiology*
  • Alzheimer Disease / genetics*
  • Female
  • Humans
  • Male
  • Membrane Transport Proteins / genetics*
  • Middle Aged
  • Mitochondrial Precursor Protein Import Complex Proteins
  • Poly T / genetics*
  • Psychotic Disorders / epidemiology*
  • Psychotic Disorders / genetics*
  • Risk Factors

Substances

  • Membrane Transport Proteins
  • Mitochondrial Precursor Protein Import Complex Proteins
  • TOMM40 protein, human
  • Poly T