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Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.
- Source :
-
European journal of neurology [Eur J Neurol] 2007 Dec; Vol. 14 (12), pp. 1344-50. Date of Electronic Publication: 2007 Oct 17. - Publication Year :
- 2007
-
Abstract
- Huntington disease (HD) is a neurodegenerative disorder due to an excessive number of CAG repeats in the IT15 gene on chromosome 4. Studies of cognitive function in asymptomatic gene carriers have yielded contradictory results. This study compared cognitive performance in 44 subjects with the HD mutation (group of carriers) who had no clinical signs of HD and 39 at-risk individuals without HD mutation (group of non-carriers). Neuropsychological evaluation focused on global cognitive efficiency, psychomotor speed, attentional, executive and memory functions. Significant differences, with lower performances in the group of gene carriers, were detected for some measures of psychomotor speed, attention and executive functioning (all P < 0.01). More differences between groups were observed for memory measures, in particular on the California Verbal Memory Test. Complementing these observations, cognitive scores were correlated with age in the group of gene carriers, but not in the group of non-carriers. This suggests that the cognitive changes precede the appearance of the motor and psychiatric symptoms in HD and that tests proved to be sensitive to early HD deficiencies are better suited than global cognitive efficiency scales to observe them.
- Subjects :
- Adolescent
Adult
Age Factors
Chromosomes, Human, Pair 4 genetics
Cognition Disorders diagnosis
Cognition Disorders physiopathology
DNA Mutational Analysis
Disease Progression
Early Diagnosis
Female
Genetic Testing
Humans
Huntingtin Protein
Huntington Disease psychology
Male
Memory Disorders diagnosis
Memory Disorders genetics
Memory Disorders physiopathology
Middle Aged
Mutation genetics
Nerve Tissue Proteins genetics
Neuropsychological Tests
Nuclear Proteins genetics
Predictive Value of Tests
Prognosis
Psychomotor Performance physiology
Sensitivity and Specificity
Cognition Disorders genetics
Genetic Predisposition to Disease genetics
Heterozygote
Huntington Disease complications
Huntington Disease genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-1331
- Volume :
- 14
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- European journal of neurology
- Publication Type :
- Academic Journal
- Accession number :
- 17941857
- Full Text :
- https://doi.org/10.1111/j.1468-1331.2007.01975.x