Replication of association between ELAVL4 and Parkinson disease: the GenePD study

Hum Genet. 2008 Aug;124(1):95-9. doi: 10.1007/s00439-008-0526-4. Epub 2008 Jun 29.

Abstract

Genetic variants in embryonic lethal, abnormal vision, Drosophila-like 4 (ELAVL4) have been reported to be associated with onset age of Parkinson disease (PD) or risk for PD affection in Caucasian populations. In the current study we genotyped three single nucleotide polymorphisms in ELAVL4 in a Caucasian study sample consisting of 712 PD patients and 312 unrelated controls from the GenePD study. The minor allele of rs967582 was associated with increased risk of PD (odds ratio = 1.46, nominal P value = 0.011) in the GenePD population. The minor allele of rs967582 was also the risk allele for PD affection or earlier onset age in the previously studied populations. This replication of association with rs967582 in a third cohort further implicates ELAVL4 as a PD susceptibility gene.

Publication types

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

MeSH terms

  • Age of Onset
  • Aged
  • Cohort Studies
  • Databases, Genetic
  • ELAV Proteins / genetics*
  • ELAV Proteins / physiology
  • ELAV-Like Protein 4
  • Female
  • Gene Frequency
  • Genetic Linkage*
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Meta-Analysis as Topic
  • Middle Aged
  • Parkinson Disease / genetics*
  • Polymorphism, Genetic

Substances

  • ELAV Proteins
  • ELAV-Like Protein 4
  • ELAVL4 protein, human