“What are my chances of having a child with autism? ”
My husband and his ex-wife have 3 sons - two teenage boys with autism and intellectual disabilities and a healthy 7-year-old boy. He and I have one healthy daughter, almost two. The risk of us having an autistic son is something like 4-12% (based on 2 siblings and a recurrence risk of 2-6% for 1 sibling which is what I found on the internet). What is the risk for a daughter? (I know it's less) And since siblings share 1/2 their genes and half-sibling share 1/4 of their genes, wouldn't our risk be slightly less than that 4-12%?
Editor’s note (6/24/2021): In the time since this article was written, we have learned a lot more about Autism Spectrum Disorder and its causes. Today, there are hundreds of genes that have been found to have some association with ASD.6-8Also, the incidence of children with ASD today is estimated to be 1 in 54.9
The genetics of autism are very complicated. There are probably lots of genes involved, most of them unknown.
Even without knowing the genes, scientists do know that it runs in families. By looking at both family studies and twin studies, scientists can figure out how likely it is that someone will get autism.
Family Risk of Autism
Half-siblings are called second-degree relatives. They share a quarter of their genes. The chance of having autism when a second-degree relative has autism are slightly increased.1 The chances of anyone in the general population having an autistic child are about 1 in 1000 or 0.1%.2 So, while the risk is real, the chances of you and your husband having an autistic child are still very low.
As I said, autism most likely involves lots of genes. Because of this, the recurrence risk is harder to figure out than you might think.
Recurrence risk is just the chance that something will happen again in the same family. If autism were caused by one gene, the recurrence risk would be the same whether you have one or more children with the disease.
The recurrence risk would be 2-6% for every child regardless of how many children you have with autism. But, because lots of genes are probably involved in autism, you need to get more than one from each of your parents.
If a couple has 2 autistic children, this suggests a "perfect storm" of autism genes. In other words, the parents have many of the same autism genes that they can pass on. This is why the recurrence risk could be 25% or more for the 3rd child rather than the 4-12% you might think.3
To get such a high chance of having an autistic child, you need both parents involved. If only one of these parents is involved the chances are much, much less.
Although we know that autism tends to run in families, we do not yet fully understand the genetics behind it. (Image via Shutterstock)
So why are the genetics of autism so complicated? Part of it has to do with the complexity of the disease.
Autism is a brain disorder that causes problems in development and can potentially cause many different symptoms. The range in symptoms makes it likely that there are several genes involved in autism.
The most recent estimate is that a person with autism could have mutations in five to ten genes.4 This means that two autistic people could have mutations in two different sets of genes. You can imagine that this makes it very difficult to study the disorder.
Twin Studies of Autism
So how can we tell if a complicated mental disorder is genetic? The best test is through twin studies.
Twin studies calculate the chances of fraternal and identical twins having the same disorder. Identical twins came from the same embryo and have the same DNA. Fraternal twins come from two embryos and only share 50% of their DNA, like siblings who are not twins.
Twin studies of autism show that there is a 36-91% chance of two identical twins being autistic. Fraternal twins, by contrast, have a very low chance of both being autistic.2 Since identical twins have the same DNA and they have a much greater chance of both being autistic, the disorder must be partly genetic.
Scientists have known for some time that autism is a genetic disorder caused by many genes. Over the past ten years scientists from all over the world have worked together to find the autism genes. Data has been collected from hundreds of families with autism. Old and new tools have been put to work to find the autism genes.
A recent study found one gene that could be involved in autism. This gene is mutated more often in people with autism. The gene codes for a protein that works in the process that makes ATP.5 ATP is the fuel or energy that cells need to function. Brain cells need a lot of energy to do their work. It's easy to imagine that if this gene were not working right, the brain cells would also not function normally. These types of results have encouraged scientists to continue their search for autism genes. The hope is that one day we may not only know your chances of having an autistic child, but also be able to cure it.
- Pickles et al. “Variable expression of the autism broader phenotype: findings from extended pedigrees.” Journal of Child Psychology and Psychiatry. (2000)
- Newschaffer et al. “Heritable and nonheritable risk factors for autism spectrum disorders.” Epidemiologic Reviews. (2002)
- Folstein & Rosen-Sheidley. “Genetics of autism: complex aetiology for a heterogeneous disorder.” Nature Reviews Genetics. (2001)
- Muhle et al. “The genetics of autism.” Pediatrics. (2004)
- Kwasnicka-Crawford et al. “Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay.” Genomics. (2005)
- O’Roak et al. “Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.” Nature. (2012)
- De Rubeis et al. “Synaptic, transcriptional and chromatin genes disrupted in autism.” Nature. (2014)
- Satterstrom et al. “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.” Cell. (2020)
- Baio et al. “Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.” MMWR Surveillance Summaries. (2018)