Prion protein codon 129 polymorphism and risk of Alzheimer disease

Neurology. 2004 Jul 27;63(2):364-6. doi: 10.1212/01.wnl.0000130198.72589.69.

Abstract

The authors investigated the PRNP Met129Val polymorphism in 1,393 subjects including 482 patients with Alzheimer disease (AD) and two independent control groups. In patients, PRNP Met homozygosity conferred increasing risk with decreasing age at onset (onset: 61 to 70 years, n = 151, p = 0.02, odds ratio [OR] = 1.72, 95% CI = 1.2 to 2.53; onset: < or =60 years, n = 138, p = 0.013, OR = 1.92, 95% CI = 1.31 to 2.87), whereas no association was obtained in patients with onset at older than 70 years. The results suggest involvement of the prion protein in the pathogenesis of early-onset AD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Aged
  • Alzheimer Disease / epidemiology
  • Alzheimer Disease / genetics*
  • Amino Acid Substitution
  • Amyloid / genetics*
  • Codon / genetics
  • Cohort Studies
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Germany / epidemiology
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Prion Proteins
  • Prions
  • Protein Precursors / genetics*
  • Risk

Substances

  • Amyloid
  • Codon
  • PRNP protein, human
  • Prion Proteins
  • Prions
  • Protein Precursors