Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan

Cerebellum. 2022 Oct;21(5):851-860. doi: 10.1007/s12311-021-01323-x. Epub 2021 Sep 9.

Abstract

The presence of fragile X mental retardation 1 (FMR1) premutation has been linked to patients with a certain type of cerebellar ataxia, the fragile X-associated tremor/ataxia syndrome (FXTAS). However, its prevalence in Japan has yet to be clarified. The aim of the present study is to determine the prevalence of FXTAS in Japanese patients with cerebellar ataxia and to describe their clinical characteristics. DNA samples were collected from 1328 Japanese patients with cerebellar ataxia, referred for genetic diagnosis. Among them, 995 patients with negative results for the most common spinocerebellar ataxia subtypes were screened for FMR1 premutation. Comprehensive clinical and radiological analyses were performed for the patients harbouring FMR1 premutation. We herein identified FMR1 premutation from one female and two male patients, who satisfied both clinical and radiological criteria of FXTAS (0.3%; 3/995) as well. Both male patients presented with high signal intensity of corticomedullary junction on diffusion-weighted magnetic resonance imaging, a finding comparable to that of neuronal intranuclear inclusion disease. The female patient mimicked multiple system atrophy in the early stages of her disease and developed aseptic meningitis with a suspected immune-mediated mechanism after the onset of FXTAS, which made her unique. Despite the lower prevalence rate in Japan than the previous reports in other countries, the present study emphasises the necessity to consider FXTAS with undiagnosed ataxia, regardless of men or women, particularly for those cases presenting with similar clinical and radiological findings with multiple system atrophy or neuronal intranuclear inclusion disease.

Keywords: Cerebellar ataxia; FMR1 premutation; FXTAS.

MeSH terms

  • Ataxia / diagnostic imaging
  • Ataxia / epidemiology
  • Ataxia / genetics
  • Cerebellar Ataxia* / diagnostic imaging
  • Cerebellar Ataxia* / epidemiology
  • Cerebellar Ataxia* / genetics
  • Female
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Syndrome* / diagnostic imaging
  • Fragile X Syndrome* / epidemiology
  • Fragile X Syndrome* / genetics
  • Humans
  • Intranuclear Inclusion Bodies
  • Japan / epidemiology
  • Male
  • Multiple System Atrophy*
  • Neurodegenerative Diseases
  • Prevalence
  • Tremor / diagnostic imaging
  • Tremor / epidemiology
  • Tremor / genetics

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein

Supplementary concepts

  • Fragile X Tremor Ataxia Syndrome
  • Neuronal intranuclear inclusion disease