Autism Studies Confirm Genetic Complexity and Risk for Older Fathers
Three of the studies, which were published in Nature, looked at new, or de novo, genetic mutations, which are not inherited but occur spontaneously around conception, in autistic children without any affected siblings. The researchers compared these children to each other and in some cases, also to their parents, and found changes in six candidate genes, three of which hadn’t previously been linked to autism.
“The basic finding is that new mutations present in sex cells carry substantial risk for autism,” says Dr. Matthew State, a professor of psychiatry at Yale, who led one of the studies.
State’s study found that 15% of autism cases in families with no other autistic children were linked to de novo mutations in either the sperm or the egg that joined during conception. The three studies overall confirmed prior research suggesting that older fathers’ sperm is more likely to carry these mutations. In one study, researchers at the University of Washington in Seattle found that the mutations were four times more likely to occur in the fathers than in the mothers — and the risk for men began increasing at age 35.
That may be because the older men are, the more times their sperm-creating cells have copied themselves, and each time a cell is copied, there is a chance that a mutation will occur. Previous studies have found that men over 50 have double the risk of having an autistic child, compared with those under 30, and the odds are four times greater for those over 55.
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In another of the Nature studies, Harvard researchers found that de novo mutations were slightly higher among autistic people than those in the general population. The findings may help explain the recent rise in autism — a government study last week put the rate of autism at 1 in 88 U.S. children — which has occurred too quickly to be explained by the spread of hereditary genes. While more than half of the risk of autism is believed to be inherited — studies find, for example, that 60% to 90% of identical twins are both autistic, sometimes to differing degrees — in at least 70% of cases of autism, a known underlying genetic cause can’t be identified.
The researchers focused on mutations that were most likely to interfere with gene function — not those that most people acquire but are harmless — thereby narrowing their search to those rare mutations that may occur only in autistic people. Then, they narrowed things further by looking at genes that had at least two such mutations. The odds that two or more mutations that cause serious problems with protein-making in the same gene also occur by chance in autism are infinitesimal.
“These are like lightning strikes in the genome,” State says, noting that the technique researchers used to find them should allow them to home in on genes that are genuinely important in the disorder. “We are [now] able to determine what the threshold should be for calling something an autism gene.”
“Now we have real path forward,” State says, explaining that “as you start to accumulate these individual genes that you know are related, that opens the door to understanding the biology.” Once you know the gene, you can examine the protein it makes. Then, even in people who don’t have the damaged gene, adding that protein may help because a deficit in that protein might result in their autism via a different pathway.
However, even though some of the newly found genes may account for a large portion of autism risk in certain individuals, overall each one has only a small affect on whether or not autism develops. State estimates from the new data that there are likely to be 500 to 1,000 genes associated with autism and that each one will account for 1% or less of the risk in the population.
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The fourth study, published in Science Translational Medicine, complicates matters even further. It found that changes in a gene that does not code for protein may also raise autism risk. Researchers found that a non-coding gene called MSNP1AS resides near a gene that does code for protein. MSN1PAS interferes with the function of that gene, which makes a protein important for brain development called moesin.
Essentially, the noncoding gene is translated into RNA that prevents the moesin gene from functioning.
Moesin plays a role in the development of connections between brain cells and how the long projections sent from one cell to another move into place. Without it, at least in a petri dish, nerve cells’ axons and dendrites “collapse,” explains Daniel Campbell, assistant professor of psychiatry at the University of Southern California and the senior author of the study.
Interestingly, mice bred to lack moesin seem outwardly normal, though no one has studied their behavior because the animals were bred specifically to study the immune system. Campbell plans to study the animals’ brains and the role moesin plays in early development.
“We’re making the hypothesis that at some point during some critical time in [brain] development the balance gets thrown off so that not enough moesin protein is made,” Campbell says. Indeed, his team found that levels of MSN1PAS were nearly 13 times higher than normal in the cortex of autistic adults examined post mortem.
Overall, the new findings will give autism researchers lots to work with, but, unfortunately, no clear answers yet for people affected by autism.
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Maia Szalavitz is a health writer at TIME.com. Find her on Twitter at @maiasz. You can also continue the discussion on TIME Healthland’s Facebook page and on Twitter at @TIMEHealthland.
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