The Role of Genetic Disruptions in Autism

Author: University of Gothenburg
Published: 2010/08/17 - Updated: 2024/08/04
Publication Details: Peer-Reviewed, Research, Study, Analysis
Topic: Autism Information - Publications List

Page Content: Synopsis - Introduction - Main

Synopsis: Study shows autism can be partially explained by abnormalities in certain genes. A survey of 1,000 individuals with autism and 1,300 without showed that Copy Number Variants (CNVs) - sub-microscopic abnormalities in the chromosomes - are heavily over-represented in autistic people.

Introduction

Together with colleagues from an international research group, autism researcher Christopher Gillberg of the University of Gothenburg, Sweden, has found in a new study that autism can be partially explained by abnormalities in certain genes. The group's results could, in the long run, pave the way for more appropriate treatments for autism.

Main Item

Prestigious journal Nature published an article co-authored by Christopher Gillberg of the Unit for Child and Adolescent Psychiatry at the Institute of Neuroscience and Physiology, and member of the Autism Genome Project (AGP) research group.

In the article the group reveals that a survey of 1,000 individuals with autism and 1,300 without showed that Copy Number Variants (CNVs) - sub-microscopic abnormalities in the chromosomes - are heavily over-represented in autistic people.

"Some of these are inherited, while others have appeared for the first time in the person with autism," says Gillberg. "Several of the abnormalities affect the genes that we have previously shown to be linked to autism and psychological developmental disorders".

The article stresses something that Gillberg and his colleagues have long asserted, namely that autism is partly down to a number of completely different genetic abnormalities, each of which occurs in just a small number of autistic people, but which together account for an increasing proportion of all cases, and that autism is an umbrella term for a large number of different neurobiological conditions that have the same symptom picture.

The study also provides evidence that other genes that are important for synapse development and intra-cellular communication (communication between the nerve cells) play a role in the origin of autism in some cases. It is hoped that the link with synapse development and intra-cellular communication will pave the way for more appropriate treatment in the long term.

"Only when we know what is actually causing the autism in each case can we customize a treatment involving medication and diet," says Gillberg.

Gillberg is also one of the initiative-takers behind AGP, a group of 120 scientists from 11 different countries who have joined forces to identify the genetic factors underlying autism. He and his colleagues in the group also published, in Nature in 2003, 2007 and 2009, the first studies to show that the mutated genes that affect the early development of synapses also cause autism in some cases.

Around one in 100 children has autism and it is more common in boys than girls. Typical symptoms are major difficulties with social interaction and rigid, stereotypical behavior starting before the age of three.

Attribution/Source(s): This peer reviewed publication was selected for publishing by the editors of Disabled World (DW) due to its relevance to the disability community. Originally authored by University of Gothenburg and published on 2010/08/17, this content may have been edited for style, clarity, or brevity. For further details or clarifications, University of Gothenburg can be contacted at gu.se/en NOTE: Disabled World does not provide any warranties or endorsements related to this article.