Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts

Acta Neurol Scand. 2006 Jan;113(1):9-13. doi: 10.1111/j.1600-0404.2005.00532.x.

Abstract

Objectives: Mutations in the Parkin gene can cause autosomal recessive early-onset Parkinson's disease (PD). Recently, Parkin mutations were also suggested to play a role in the commoner late-onset forms of PD.

Methods: We compared a German cohort of PD patients (95) with a Norwegian cohort of PD patients (96). Both cohorts have predominant late-onset form of PD. Mutation and polymorphism frequencies were compared via single-strand conformation polymorphism and sequence analyses.

Results: Three heterozygous missense mutations (Arg256Cys, Arg402Cys and Thr240Met) were found in late-onset PD patients in the German patient cohort (1.6%). A missense mutation (Arg402Cys) was also found in one of 149 healthy control subjects (0.3%). Only one heterozygous missense mutation (Arg256Cys) was identified in a Norwegian patient suffering from late-onset PD (0.5%). The frequencies of four known single nucleotide polymorphisms significantly differ between the two distant European populations.

Conclusion: The results support the hypothesis that heterozygous mutations in the Parkin gene may act as susceptibility alleles for late-onset forms of PD in rare cases.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Cohort Studies
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Germany
  • Heterozygote
  • Humans
  • Introns / genetics
  • Middle Aged
  • Mutation, Missense*
  • Norway
  • Parkinson Disease / genetics*
  • Polymorphism, Single Nucleotide*
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Ubiquitin-Protein Ligases
  • parkin protein