Washington: Scientists have identified two additional genes that may be associated with autism.
Study co-author Ning Lei, a researcher at Princeton University and the Institute for Advanced Studies, said that there is no known cause of autism, but mutations of several genes have been linked to autism.
For the study, Dr. Lei and her colleagues analyzed data from the Autism Genetic Resource Exchange (AGRE) on 943 families, most of whom had more than one child diagnosed with autism and had undergone genetic testing.
The researchers compared the prevalence of 25 gene mutations in the AGRE families with a control group of 6,317 individuals without developmental or neuropsychiatric illness.
The researchers identified mutations in four genes within the AGRE families. Two of the genes previously were shown to be associated with autism and often are involved in forming or maintaining neural synapses — the point of connection between individual neurons.
One of the new genes identified was neural cell adhesion molecule 2 (NCAM2). NCAM2 is expressed in the hippocampus of the human brain — a region previously associated with autism.
"While mutations in the NCAM2 gene were found in a small percentage of the children that we studied, it is fascinating that this finding continues a consistent story — that many of the genes associated with autism are involved with formation or function of the neural synapse. Studies such as this provide evidence that autism is a genetically based disease that affects neural connectivity," Dr. Lei said.
The researchers hypothesize that a substantial percentage of children with autism will be shown to have a mutation in one or more of the many genes necessary for normal function of the synapse.
The study also showed that some parents and siblings of children with autism have the NCAM2 mutation but do not have the disorder themselves.
This suggests that other environmental or genetic factors are involved in causing autism in susceptible individuals.
"These results help the public understand that autism is a very complex disorder, much like cancer and no single gene or gene environment is likely to be causative in most cases," Dr. Lei said.
The findings have been presented at the Pediatric Academic Societies (PAS) annual meeting in Vancouver, British Columbia, Canada.