No association of common VCP variants with sporadic frontotemporal dementia

Neurobiol Aging. 2009 Feb;30(2):333-5. doi: 10.1016/j.neurobiolaging.2007.05.023. Epub 2007 Jul 5.

Abstract

Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD). To investigate the role of this novel gene in sporadic forms of frontotemporal dementia (FTD), we genotyped 27 single nucleotide polymorphisms covering the entire VCP genomic region in 198 patients with sporadic FTD and 184 matched controls from Germany. No significant association could be demonstrated. There is no evidence, that common variants in VCP confer a strong risk to the development of sporadic FTD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Cell Cycle Proteins / genetics*
  • Dementia / epidemiology*
  • Dementia / genetics*
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genetic Variation
  • Germany / epidemiology
  • Humans
  • Incidence
  • Male
  • Polymorphism, Single Nucleotide / genetics*
  • Risk Assessment / methods*
  • Risk Factors
  • Valosin Containing Protein

Substances

  • Cell Cycle Proteins
  • Adenosine Triphosphatases
  • VCP protein, human
  • Valosin Containing Protein