Association study between late-onset Alzheimer's disease and the transferrin gene polymorphisms in Chinese

Neurosci Lett. 2003 Oct 9;349(3):209-11. doi: 10.1016/s0304-3940(03)00837-1.

Abstract

To investigate the possible involvement of the transferrin (TF) gene polymorphism in the manifestation of Alzheimer's disease (AD), we analyzed the TF and apolipoprotein E (APOE) genotypes of 67 sporadic late-onset AD patients and 131 normal elderly controls in the Chinese population. Our data showed that the TF C1 homozygosity carriers had an increased risk of AD in subjects > or =75 years of age, showing that homozygosity for the TF C1 allele was associated with an approximately three-fold increased risk (OR=3.57, 95% CI, 1.24-10.27, P=0.014). No synergic effects were found between the APOE epsilon 4 allele and TF gene polymorphisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aged
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism
  • Apolipoprotein E4
  • Apolipoproteins E / genetics*
  • Brain / metabolism*
  • Brain / physiopathology
  • Brain Chemistry / genetics*
  • China / ethnology
  • DNA Mutational Analysis
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genotype
  • Humans
  • Male
  • Polymorphism, Genetic / genetics*
  • Risk Factors
  • Transferrin / genetics*

Substances

  • Apolipoprotein E4
  • Apolipoproteins E
  • Transferrin