Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings

Acta Neurol Scand. 2008 Jan;117(1):41-8. doi: 10.1111/j.1600-0404.2007.00904.x.

Abstract

Objectives: The objectives of this study were to: (i) establish whether the spinocerebellar ataxia type 8 (SCA 8) expansion is associated with ataxia in Scotland; (ii) test the hypothesis that SCA 8 is associated with neuropsychological impairment; and (iii) review neuroradiological findings in SCA 8.

Methods: The methods included: (i) measurement of SCA 8 expansion frequencies in ataxic patients and healthy controls; (ii) comprehensive neuropsychological assessment of patients with SCA 8 and matched controls, neuropsychiatric interview; and (iii) comparison of patient and matched control magnetic resonance imaging (MRI) scans.

Results: (i) 10/694 (1.4%) unrelated individuals with ataxia had combined CTA/CTG repeat expansions >100 compared to 1/1190 (0.08%) healthy controls (P < 0.0005); (ii) neuropsychological assessment revealed a dysexecutive syndrome among SCA 8 patients, not readily explained by motor or mood disturbance; neuropsychiatric symptoms occurred commonly; (iii) cerebellar atrophy was the only salient MRI abnormality in the patient group.

Conclusions: The SCA 8 expansion is associated with ataxia in Scotland. The disorder is associated with a dysexecutive syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cerebellum / pathology
  • Cerebellum / physiopathology
  • Cognition / physiology
  • Cognition Disorders / diagnosis
  • Cognition Disorders / etiology
  • Cognition Disorders / physiopathology
  • DNA Mutational Analysis
  • Female
  • Gene Frequency
  • Genetic Markers
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mental Disorders / diagnosis*
  • Mental Disorders / etiology*
  • Middle Aged
  • Nerve Tissue Proteins / genetics*
  • Neuropsychological Tests
  • RNA, Long Noncoding
  • RNA, Untranslated
  • Scotland
  • Spinocerebellar Ataxias / complications*
  • Spinocerebellar Ataxias / genetics*
  • Spinocerebellar Ataxias / psychology
  • Trinucleotide Repeat Expansion / genetics

Substances

  • ATXN8OS gene product, human
  • Genetic Markers
  • Nerve Tissue Proteins
  • RNA, Long Noncoding
  • RNA, Untranslated