Cerebrospinal fluid fatty acids in glucocerebrosidase-associated Parkinson's disease

Mov Disord. 2012 Feb;27(2):288-92. doi: 10.1002/mds.23984. Epub 2011 Oct 21.

Abstract

Background: Heterozygous mutations in the glucocerebrosidase gene lead to an increased risk for and to more severe alpha-synuclein-associated pathology in Parkinson's disease. As both glucocerebrosidase and alpha-synuclein interact with fatty acids, we hypothesized that cerebrospinal fluid fatty acid levels are altered in these Parkinson's disease patients.

Methods: Cerebrospinal fluid levels of 13 fatty acids in 8 Parkinson's disease patients with a heterozygous glucocerebrosidase mutation were compared with those of 41 idiopathic Parkinson's disease patients and 30 controls using gas chromatography.

Results: Parkinson's disease patients with a heterozygous glucocerebrosidase mutation had lower levels of palmitoleic (P ≤ .007), oleic (P ≤ .016), linoleic (P ≤ .005), arachidonic (P ≤ .003), eicosapentaenoic (P ≤ .003) and decosahexaenoic (P ≤ .03) acids and lower levels of total fatty acids (P < .005) compared with both idiopathic Parkinson's disease patients and control subjects.

Conclusions: These results suggest that abnormalities of fatty acid metabolism are specifically involved in the pathogenesis of Parkinson's disease associated with a heterozygous glucocerebrosidase mutation.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Fatty Acids / cerebrospinal fluid*
  • Female
  • Glucosylceramidase / genetics*
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Parkinson Disease / cerebrospinal fluid*
  • Parkinson Disease / genetics*

Substances

  • Fatty Acids
  • Glucosylceramidase