Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

Mov Disord. 2005 Jan;20(1):100-3. doi: 10.1002/mds.20320.

Abstract

Mutations in the beta-glucocerebrosidase gene cause Gaucher's disease, one of the most common lysosomal lipid storage diseases in the Ashkenazi Jewish population. The occurrence of parkinsonism in patients with Type 1 Gaucher's disease has been noted previously. In this pilot study, we evaluated a possible association between Parkinson's disease (PD) and the beta-glucocerebrosidase gene N370S allele (nt.1226 A>G) in 160 Parkinson's disease patients and 92 controls of Jewish ethnicity. We observed a higher frequency of the N370S genotype in PD cases (NS and SS, 10.7%) compared to controls (NS and SS 4.3%); however, the difference was not statistically significant (chi(2) = 3.4, P = 0.2). A total of 17 PD cases carry the N370S allele, including 2 homozygotes and 15 heterozygotes. The N370S allele (nt.1226 A>G) may be associated with PD in patients of Jewish ethnicity and should be examined in a larger study.

Publication types

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

MeSH terms

  • Aged
  • Alleles*
  • Aspartic Acid / genetics*
  • DNA Mutational Analysis
  • Female
  • Gene Frequency
  • Genotype
  • Glucosylceramidase / genetics*
  • Humans
  • Jews
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Parkinson Disease / genetics*
  • Pilot Projects
  • Point Mutation
  • Serine / genetics

Substances

  • Aspartic Acid
  • Serine
  • Glucosylceramidase