TREM2 rare variant p.R47H is not associated with Parkinson's disease

Parkinsonism Relat Disord. 2016 Feb:23:109-11. doi: 10.1016/j.parkreldis.2015.11.026. Epub 2015 Nov 25.

Abstract

Variant p.R47H of triggering receptor expressed on myeloid cells 2 (TREM2) has been associated with Parkinson's disease (PD). We screened this TREM2-variant in 821 PD patients including 261 demented PD patients (PDD) and in healthy controls (n = 919). Neither the entire PD nor the small PDD sample was associated with p.R47H.

Keywords: Association; Dementia; Non-motor symptoms; Parkinson's disease; TREM2.

Publication types

  • Letter
  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genetic Variation
  • Humans
  • Male
  • Membrane Glycoproteins / genetics*
  • Middle Aged
  • Parkinson Disease / genetics*
  • Polymorphism, Single Nucleotide
  • Receptors, Immunologic / genetics*

Substances

  • Membrane Glycoproteins
  • Receptors, Immunologic
  • TREM2 protein, human