GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease

Eur J Neurol. 2009 Aug;16(8):909-11. doi: 10.1111/j.1468-1331.2009.02621.x. Epub 2009 Mar 31.

Abstract

Background and purpose: A single nucleotide polymorphism in the 3'-untranslated region of the progranulin gene (GRN; 3'UTR+78C>T; rs5848) was reported to alter the risk for frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U). rs5848 is located within a micro-RNA binding site and affects the expression of GRN.

Methods: As FTLD-U patients often present with parkinsonism, we investigated the association of GRN rs5848 and risk of Parkinson's disease in two Caucasian patient-control series (n = 1413) from the US and Poland.

Results: No association was observed between rs5848 and susceptibility to Parkinson's disease (individual series and combined analysis).

Conclusions: This finding shows that GRN rs5848 does not affect the risk of Parkinson's disease in the US and Polish populations.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Male
  • Middle Aged
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics*
  • Poland / epidemiology
  • Polymorphism, Single Nucleotide*
  • Progranulins
  • Risk Factors
  • United States / epidemiology
  • White People / genetics
  • Young Adult

Substances

  • GRN protein, human
  • Intercellular Signaling Peptides and Proteins
  • Progranulins