The causes of autism spectrum disorder or ASD are not fully understood; researchers believe both genetics and environment play a role. In some cases, the disorder is linked to de novo mutations that appear only in the child and are not inherited from either parent's DNA.

In a study published in Nature Medicine, an international team of scientists describe a method to measure disease-causing mutations found only in the sperm of the father, providing a more accurate assessment of ASD risk in future children.

"Autism afflicts 1 in 59 children and we know that a significant portion is caused by these de novo DNA mutations, yet we are still blind to when and where these mutations will occur," said co-senior author. "With our new study, we can trace some of these mutations back to the father, and we can directly assess the risk of these same mutations occurring again in future children."

Recent studies suggest gene-damaging de novo mutations are involved in at least 10 to 30 percent of ASD cases, with the number of mutations rising with the father's age at time of conception. De novo mutations occur spontaneously in parents' sperm or eggs or during fertilization. The mutation is then present in each cell as the fertilized egg divides. Studies now point to male sperm as a particularly important source of these mutations, with the chance of the mutation recurring within the same family generally estimated at 1 to 3 percent.

"However, such estimates are not based on actual knowledge of the risk in an individual family, but instead are based on frequencies in the general population," said the other co-senior study author. "When a disease-causing mutation occurs for the first time in a family, the probability that it could happen again in future offspring is not known. Thus families must make a decision with a great deal of uncertainty."

For their study, the authors analyzed the sperm of eight fathers who were already parents of children with ASD. The goal was to look for the presence of multiple, genetically different material in cells in the same person, a phenomenon called mosaicism. Using deep whole genome sequencing, they found variants in offspring that were matched only in the fathers' sperm.

"While medical textbooks teach us that every cell in the body has an identical copy of DNA, this is fundamentally not correct. Mutations occur every time a cell divides, so no two cells in the body are genetically identical," said the first author.

"Mosaicism can cause cancer or can be silent in the body. If a mutation occurs early in development, then it will be shared by many cells within the body. But if a mutation happens just in sperm, then it can show up in a future child but not cause any disease in the father."

The researchers determined that disease-causing mutations were present in up to 15 percent of the fathers' sperm cells, information that could not be determined through other means, such as blood samples.

"My laboratory has a long-standing interest in understanding the origins of pediatric brain disease, and how mutations contributes to disease in a child," said the co-senior author. "We previously showed that mosaicism in a child can lead to diseases like epilepsy. Here, we show that mosaicism in one of parents is at least as important when thinking about genetic counseling."

If developed into a clinical test, the researchers said fathers could have their sperm studied to determine their precise risk of recurrence in future children. The methods might also be applied to men that haven't had children yet, but who want to know the risk of having a child with a disease.

https://ucsdnews.ucsd.edu/pressrelease/measuring-mutations-in-sperm-may-reveal-risk-for-autism-in-future-children

https://www.nature.com/articles/s41591-019-0711-0