Apolipoprotein E epsilon 4 in inclusion body myositis

Ann Neurol. 1995 Dec;38(6):957-9. doi: 10.1002/ana.410380619.

Abstract

The genetic predisposition to inclusion body myositis (IBM) is probably multifactorial. The deposition of the beta-amyloid protein is a characteristic histological feature of both IBM and Alzheimer's disease (AD). The epsilon 4 allele of apolipoprotein E (APO E) has been strongly associated with familial and late-onset AD. We therefore compared the APO E allele frequencies in a group of 14 patients with IBM with those in a group of patients with other inflammatory muscle diseases and in the general population. The frequency of the epsilon 4 allele in IBM was increased (0.29) compared with that in patients with other inflammatory muscle diseases (0.15) and the general population (0.13) (p < 0.05). These data suggest that APO E genotype may be one of the factors involved in determining the predisposition to the development of IBM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Alleles
  • Apolipoproteins E / genetics*
  • Female
  • Genotype
  • Humans
  • Inclusion Bodies, Viral / genetics
  • Male
  • Middle Aged
  • Myositis, Inclusion Body / genetics*
  • Sex Distribution

Substances

  • Apolipoproteins E