Genetic association of a cathepsin D polymorphism and sporadic Creutzfeldt-Jakob disease

Dement Geriatr Cogn Disord. 2009;28(4):302-6. doi: 10.1159/000246343. Epub 2009 Oct 13.

Abstract

Background: Cathepsin D is the most abundant lysosomal and endosomal aspartyl protease; it shows beta and gamma secretase activity in vitro by cleaving the amyloid precursor protein into amyloid beta protein. In recent studies, cathepsin D was co-localized with PrP(Sc), the disease-associated form of the prion disease, and abnormal expression of cathepsin D correlated with tissue damage in brains of sporadic Creutzfeldt-Jakob disease (CJD).

Objective: To investigate whether a polymorphism at position 224, C224T, on exon 2 of the cathepsin D gene (CTSD) is associated with sporadic CJD in the Korean population.

Methods: We compared the genotype and allele frequencies at this polymorphism site in 172 sporadic CJD patients with those in 197 healthy Koreans.

Results and conclusion: Our study does not show a significant difference in genotype (p = 0.901) and allele (p = 0.509) frequencies of CTSD C224T between sporadic CJD patients and normal controls. This was the first genetic association study of CTSD in a sporadic CJD population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Aged
  • Alleles
  • Cathepsin D / genetics*
  • Creutzfeldt-Jakob Syndrome / genetics*
  • DNA / genetics
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Korea / epidemiology
  • Male
  • Middle Aged
  • Polymorphism, Genetic

Substances

  • DNA
  • Cathepsin D