Unknown

Dataset Information

0

Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes.


ABSTRACT: BACKGROUND: The etiology of autism spectrum disorders (ASD) is largely determined by different genetic factors of variable impact. This genetic heterogeneity could be a factor to explain the clinical heterogeneity of autism spectrum disorders. Here, a first attempt is made to assess whether genetically more homogeneous ASD groups are associated with decreased phenotypic heterogeneity with respect to their autistic symptom profile. METHODOLOGY: The autistic phenotypes of ASD subjects with 22q11 deletion syndrome (22q11DS) and ASD subjects with Klinefelter Syndrome (KS) were statistically compared to the symptom profile of a large (genetically) heterogeneous ASD sample. Autism diagnostic interview-revised (ADI-R) variables were entered in different statistical analyses to assess differences in symptom homogeneity and the feasibility of discrimination of group-specific ASD-symptom profiles. PRINCIPAL FINDINGS: The results showed substantially higher symptom homogeneity in both the genetic disorder ASD groups in comparison to the heterogeneous ASD sample. In addition, a robust discrimination between 22q11-ASD and KS-ASD and idiopathic ASD phenotypes was feasible on the basis of a reduced number of autistic scales and symptoms. The lack of overlap in discriminating subscales and symptoms between KS-ASD and 22q11DS-ASD suggests that their autistic symptom profiles cluster around different points in the total diagnostic space of profiles present in the general ASD population. CONCLUSION: The findings of the current study indicate that the clinical heterogeneity of ASDs may be reduced when subgroups based on a specific genotype are extracted from the idiopathic ASD population. The current strategy involving the widely used ADI-R offers a relatively straightforward possibility for assessing genotype-phenotype ASD relationships. Reverse phenotype strategies are becoming more feasible, given the accumulating evidence for the existence of genetic variants of large effect in a substantial proportion of the ASD population.

SUBMITTER: Bruining H 

PROVIDER: S-EPMC2878316 | biostudies-literature | 2010

REPOSITORIES: biostudies-literature

altmetric image

Publications

Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes.

Bruining Hilgo H   de Sonneville Leo L   Swaab Hanna H   de Jonge Maretha M   Kas Martien M   van Engeland Herman H   Vorstman Jacob J  

PloS one 20100528 5


<h4>Background</h4>The etiology of autism spectrum disorders (ASD) is largely determined by different genetic factors of variable impact. This genetic heterogeneity could be a factor to explain the clinical heterogeneity of autism spectrum disorders. Here, a first attempt is made to assess whether genetically more homogeneous ASD groups are associated with decreased phenotypic heterogeneity with respect to their autistic symptom profile.<h4>Methodology</h4>The autistic phenotypes of ASD subjects  ...[more]

Similar Datasets

| S-EPMC5789213 | biostudies-literature
| PRJEB34754 | ENA
| S-EPMC4125617 | biostudies-other
| S-EPMC3812662 | biostudies-literature
| S-EPMC7457751 | biostudies-literature
| S-EPMC4247857 | biostudies-literature
2018-12-14 | GSE107896 | GEO
| S-EPMC8267579 | biostudies-literature
2014-11-22 | E-GEOD-63524 | biostudies-arrayexpress
2010-05-17 | E-GEOD-15402 | biostudies-arrayexpress