A neuropsychological investigation of male premutation carriers of fragile X syndrome

Caroline J. Moore, Eileen M. Daly, Nicole Schmitz, Flora Tassone, Carolyn Tysoe, Randi J Hagerman, Paul J Hagerman, Robin G. Morris, Kieran C. Murphy, Declan G M Murphy

Research output: Contribution to journalArticle

95 Citations (Scopus)

Abstract

It is currently thought that fragile X syndrome (FraX; the most common inherited form of learning disability) results from having more than 200 cytosine-guanine-guanine (CGG) trinucleotide repeats, with consequent methylation of the fragile X mental retardation (FMR1) gene and loss of FMR1 protein (FMRP). It was also considered that premutation carriers (with 55-200 CGG repeats) are unaffected, although a tremor/ataxia syndrome has recently been described in older adult male carriers. We reported that premutation expansion of CGG trinucleotide repeats affects brain anatomy, which, together with other studies, indicates that the molecular model for FraX needs modification. However, there are few studies on the cognitive ability of adult male premutation carriers. Thus, we selected 20 male premutation carriers on the basis of their genetic phenotype, and compared them to 20 male controls matched on age, IQ and handedness. We investigated intellectual functioning, executive function, memory, attention, visual and spatial perception, and language and pragmatics. The premutation carriers had significant impairments on tests of executive function (Verbal Fluency, Trail Making Test and Tower of London) and memory (Names sub-test of the Doors and People, Verbal Paired Associates Immediate Recall and Visual Paired Associates Delayed Recall sub-tests of the WMS-R, and Category Fluency Test for natural kinds). We therefore suggest that CGG trinucleotide repeats in the premutation range affect specific neuronal circuits that are concordant with specific neuropsychological deficits; and that these deficits reflect an emerging neuropsychological phenotype of premutation FraX.

Original languageEnglish (US)
Pages (from-to)1934-1947
Number of pages14
JournalNeuropsychologia
Volume42
Issue number14
DOIs
StatePublished - 2004

Fingerprint

Fragile X Syndrome
Guanine
Cytosine
Trinucleotide Repeats
Executive Function
Trail Making Test
Phenotype
Functional Laterality
Visual Perception
Molecular Models
Aptitude
Learning Disorders
Tremor
Ataxia
Short-Term Memory
Intellectual Disability
Methylation
Names
Anatomy
Language

Keywords

  • Executive function
  • Memory
  • Trinucleotide repeats
  • X chromosome

ASJC Scopus subject areas

  • Behavioral Neuroscience
  • Neuropsychology and Physiological Psychology

Cite this

A neuropsychological investigation of male premutation carriers of fragile X syndrome. / Moore, Caroline J.; Daly, Eileen M.; Schmitz, Nicole; Tassone, Flora; Tysoe, Carolyn; Hagerman, Randi J; Hagerman, Paul J; Morris, Robin G.; Murphy, Kieran C.; Murphy, Declan G M.

In: Neuropsychologia, Vol. 42, No. 14, 2004, p. 1934-1947.

Research output: Contribution to journalArticle

Moore, Caroline J. ; Daly, Eileen M. ; Schmitz, Nicole ; Tassone, Flora ; Tysoe, Carolyn ; Hagerman, Randi J ; Hagerman, Paul J ; Morris, Robin G. ; Murphy, Kieran C. ; Murphy, Declan G M. / A neuropsychological investigation of male premutation carriers of fragile X syndrome. In: Neuropsychologia. 2004 ; Vol. 42, No. 14. pp. 1934-1947.
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