Literature DB >> 16721319

Genetic heterogeneity between the three components of the autism spectrum: a twin study.

Angelica Ronald1, Francesca Happé2, Patrick Bolton2, Lee M Butcher2, Thomas S Price2, Sally Wheelwright2, Simon Baron-Cohen2, Robert Plomin2.   

Abstract

OBJECTIVE: This study investigated the etiology of autistic-like traits in the general population and the etiological overlap between the three aspects of the triad of impairments (social impairments, communication impairments, restricted repetitive behaviors and interests) that together define autism spectrum disorders.
METHOD: Parents of 3,400 8-year-old twin pairs from the Twins Early Development Study completed the Childhood Asperger Syndrome Test, a screening instrument for autism spectrum symptoms in mainstream samples. Genetic model-fitting of categorical and continuous data is reported.
RESULTS: High heritability was found for extreme autistic-like traits (0.64-0.92 for various cutoffs) and autistic-like traits as measured on a continuum (0.78-0.81), with no significant shared environmental influences. All three subscales were highly heritable but showed low covariation. In the genetic modeling, distinct genetic influences were identified for the three components.
CONCLUSIONS: These results suggest the triad of impairments that define autism spectrum disorders is heterogeneous genetically. Molecular genetic research examining the three components separately may identify different causal pathways for the three components. The analyses give no indication that different genetic processes affect extreme autistic impairments and autistic impairments as measured on a continuum, but this can only be directly tested once genes are identified.

Entities:  

Mesh:

Year:  2006        PMID: 16721319     DOI: 10.1097/01.chi.0000215325.13058.9d

Source DB:  PubMed          Journal:  J Am Acad Child Adolesc Psychiatry        ISSN: 0890-8567            Impact factor:   8.829


  178 in total

1.  Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.

Authors:  Judith S Nijmeijer; Alejandro Arias-Vásquez; Nanda N J Rommelse; Marieke E Altink; Richard J L Anney; Philip Asherson; Tobias Banaschewski; Cathelijne J M Buschgens; Ellen A Fliers; Michael Gill; Ruud B Minderaa; Luise Poustka; Joseph A Sergeant; Jan K Buitelaar; Barbara Franke; Richard P Ebstein; Ana Miranda; Fernando Mulas; Robert D Oades; Herbert Roeyers; Aribert Rothenberger; Edmund J S Sonuga-Barke; Hans-Christoph Steinhausen; Stephen V Faraone; Catharina A Hartman; Pieter J Hoekstra
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-05-20       Impact factor: 8.829

2.  A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.

Authors:  Maria C N Marchetto; Cassiano Carromeu; Allan Acab; Diana Yu; Gene W Yeo; Yangling Mu; Gong Chen; Fred H Gage; Alysson R Muotri
Journal:  Cell       Date:  2010-11-12       Impact factor: 41.582

Review 3.  Developmental neurogenetics and multimodal neuroimaging of sex differences in autism.

Authors:  Christina Chen; John Darrell Van Horn
Journal:  Brain Imaging Behav       Date:  2017-02       Impact factor: 3.978

Review 4.  Genetics in child and adolescent psychiatry: methodological advances and conceptual issues.

Authors:  Sarah Hohmann; Nicoletta Adamo; Benjamin B Lahey; Stephen V Faraone; Tobias Banaschewski
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-04-08       Impact factor: 4.785

5.  The Relationship Between Subthreshold Autistic Traits, Ambiguous Figure Perception and Divergent Thinking.

Authors:  Catherine Best; Shruti Arora; Fiona Porter; Martin Doherty
Journal:  J Autism Dev Disord       Date:  2015-12

6.  Variants in several genomic regions associated with asperger disorder.

Authors:  D Salyakina; D Q Ma; J M Jaworski; I Konidari; P L Whitehead; R Henson; D Martinez; J L Robinson; S Sacharow; H H Wright; R K Abramson; J R Gilbert; M L Cuccaro; M A Pericak-Vance
Journal:  Autism Res       Date:  2010-12       Impact factor: 5.216

7.  Glyoxalase I polymorphism rs2736654 causing the Ala111Glu substitution modulates enzyme activity--implications for autism.

Authors:  Madhabi Barua; Edmund C Jenkins; Wenqiang Chen; Salomon Kuizon; Raju K Pullarkat; Mohammed A Junaid
Journal:  Autism Res       Date:  2011-04-12       Impact factor: 5.216

8.  Quantitative linkage for autism spectrum disorders symptoms in attention-deficit/hyperactivity disorder: significant locus on chromosome 7q11.

Authors:  Judith S Nijmeijer; Alejandro Arias-Vásquez; Nanda N J Rommelse; Marieke E Altink; Cathelijne J M Buschgens; Ellen A Fliers; Barbara Franke; Ruud B Minderaa; Joseph A Sergeant; Jan K Buitelaar; Pieter J Hoekstra; Catharina A Hartman
Journal:  J Autism Dev Disord       Date:  2014-07

9.  Exploring the relationship between autistic-like traits and ADHD behaviors in early childhood: findings from a community twin study of 2-year-olds.

Authors:  Angelica Ronald; Lisa R Edelson; Philip Asherson; Kimberly J Saudino
Journal:  J Abnorm Child Psychol       Date:  2010-02

10.  Pathogenesis of autism: a patchwork of genetic causes.

Authors:  Elena L Grigorenko
Journal:  Future Neurol       Date:  2009
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.