Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease

J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):478-80. doi: 10.1136/jnnp.2003.015750.

Abstract

Background: The Saitohin gene has recently been identified in intron 9 of the Tau gene. Because an association between Parkinson's disease and Tau has been described, Saitohin represents a candidate gene for Parkinson's disease.

Objective: To test these two genes for their association with Parkinson's disease in a large community based case-control study.

Results: Cases (n = 208) were more often homozygotes for the Tau H1 haplotype than controls (n = 483; odds ratio (OR) = 1.71 (95% confidence interval, 1.20 to 2.43); p = 0.003), and the saitohin Q allele was in complete linkage disequilibrium with the H1 haplotype. This association was stronger among cases with Parkinson's disease onset below 65 years (< or =65 years: OR = 2.52 (1.49 to 4.25); p<0.001) than among those with older onset (>65 years: OR = 1.20 (0.73 to 1.98); p<0.47).

Conclusions: The data suggest that there is a functional polymorphism at this locus involved in Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease*
  • Haplotypes
  • Humans
  • Male
  • Middle Aged
  • Odds Ratio
  • Parkinson Disease / genetics*
  • Parkinson Disease / pathology
  • Polymorphism, Genetic*
  • tau Proteins / genetics*

Substances

  • STH protein, human
  • tau Proteins