Behavioural and cognitive phenotypes in idiopathic autism versus autism associated with fragile X syndrome
- 11 March 2009
- journal article
- Published by Wiley in Journal of Child Psychology and Psychiatry
- Vol. 50 (3) , 290-299
- https://doi.org/10.1111/j.1469-7610.2008.01988.x
Abstract
Background: In order to better understand the underlying biological mechanism/s involved in autism, it is important to investigate the cognitive and behavioural phenotypes associated with idiopathic autism (autism without a known cause) and comorbid autism (autism associated with known genetic/biological disorders such as fragile X syndrome). Parental effects associated with each type of autism also serve to cast light on the biological underpinnings of autism.Method: Forty‐nine participants with idiopathic autism (AD; Mean age: 11.16; SD: 6.08) and their parents (45 mothers; 34 fathers), and 48 participants with fragile X syndrome and co‐morbid autism (FXS/AD; Mean age: 17.30; SD: 10.22) and their parents (32 mothers; 30 fathers) were administered the ADOS‐G and the age‐appropriate Wechsler test to ascertain autism and cognitive profiles respectively.Results: The AD and FXS/AD groups showed a similar profile on the ADOS domains, with slightly higher scores on the Communication domain in the FXS/AD group, after adjusting for full‐scale IQ. Marked differences between the groups in their cognitive abilities were apparent, with the FXS/AD group showing significantly lower scores on all subtests except Comprehension. While no parental effects were found for the FXS/AD group, a paternal effect was apparent on the combined ADOS score for the AD group. Moreover, midparental effects were found in this group for full‐scale IQ (FSIQ) and verbal IQ (VIQ). Analyses also revealed parental effects for the subtests of Similarities, Vocabulary, and Information with predominantly maternal effect, and Digit Span with predominantly paternal effect. Both parents contributed to the midparental effect for Processing Speed.Conclusions: The results, together with our previous findings, suggest that the postulated combination of susceptibility genes for autism may primarily involve cognitive rather than behavioural processes.Keywords
This publication has 56 references indexed in Scilit:
- Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorderEuropean Psychiatry, 2007
- Molecular and cognitive predictors of the continuum of autistic behaviours in fragile XNeuroscience & Biobehavioral Reviews, 2006
- Constitutional Downregulation of SEMA5A Expression in AutismNeuropsychobiology, 2006
- Phenotypic variation and FMRP levels in fragile XMental Retardation and Developmental Disabilities Research Reviews, 2004
- Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autismNature Genetics, 2003
- The broad autism phenotype: A complementary strategy for molecular genetic studies of autismAmerican Journal of Medical Genetics, 2001
- Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary reportAmerican Journal of Medical Genetics, 1999
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Developmental issues in fragile X syndromePublished by Cambridge University Press (CUP) ,1990