Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions

Neurobiol Aging. 2015 Feb;36(2):1223.e1-2. doi: 10.1016/j.neurobiolaging.2014.08.033. Epub 2014 Sep 6.

Abstract

Multiple system atrophy (MSA) is a fatal neurodegenerative disorder of unknown etiology that presents with variable combinations of progressive ataxia, parkinsonism, and autonomic instability. Pathologic expansion of a hexanucleotide repeat in the C9orf72 gene has been demonstrated to cause neurodegeneration with diverse neurologic presentations. To test the hypothesis whether pathologic expansions in C9orf72 are a cause of MSA, we undertook genetic screening in 100 neuropathologically confirmed cases. No pathologic repeat expansions were detected suggesting that MSA is not a C9orf72-related neurodegenerative disease.

Keywords: Amyotrophic lateral sclerosis; C9orf72; Fronto-temporal dementia; Multiple system atrophy; Neurodegeneration.

MeSH terms

  • C9orf72 Protein
  • Cohort Studies
  • DNA Repeat Expansion / genetics*
  • Genetic Testing
  • Humans
  • Multiple System Atrophy / genetics*
  • Proteins / genetics*

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • Proteins