Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia

Prion. 2019 Jan;13(1):116-123. doi: 10.1080/19336896.2019.1617027.

Abstract

Background: Fatal familial insomnia (FFI) is a rare autosomal-dominant inherited prion disease characterized clinically by severe sleep disorder, motor signs, dysautonomia and abnormal behaviour. FFI is caused by a missense mutation at codon 178 of the prion protein gene (PRNP). Our study is aimed to explore typical clinical and genetic features of two Chinese pedigrees with FFI and review the related literatures. Methods: Two FFI cases with family histories were recruited in our study. The main clinical features, genetic features and possible pathophysiologic mechanisms of these two FFI cases were analysed. Results: The foremost symptoms seemed to be sleep disturbances and psychosis. Progressive sympathetic symptoms, movement disturbances and memory loss were frequently observed as well. Electroencephalography (EEG) showed a minor slowing without periodic triphasic waves. Polysomnography (PSG) showed reduction in total sleep time and disturbance of sleep-related respiratory. Brain magnetic resonance imaging (MRI) did not reveal obvious abnormality. Genetic analysis disclosed the prion protein gene mutation at codon 178 (D178N), with methionine (Met) homozygosity at the polymorphic position 129 (Met129Met). Conclusions: The major clinical features of Chinese FFI are sleep dysfunction, psychiatric symptoms and sympathetic symptoms. Our patients have similar clinical characteristics as that of the typical FFI cases.

Keywords: Fatal family insomnia; PRNP; clinical features; gene mutation; genetic characteristics; pedigree; thalamus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Asian People / genetics
  • Brain / physiopathology
  • China / epidemiology
  • Female
  • Humans
  • Insomnia, Fatal Familial / complications
  • Insomnia, Fatal Familial / genetics*
  • Insomnia, Fatal Familial / physiopathology*
  • Male
  • Middle Aged
  • Pedigree
  • Point Mutation
  • Prion Proteins / genetics*
  • Psychotic Disorders / etiology
  • Retrospective Studies
  • Young Adult

Substances

  • Prion Proteins

Grants and funding

This work was supported by the National Natural Science Foundation of China [81401059]; National Natural Science Foundation of China [81401060].