Published on Monday, August 15, 2016
Media Contact: Karen Bascom at 601-815-3940 or firstname.lastname@example.org.
When Laura Beth Johnston's son Fraiser was diagnosed with autism in December 2014, she said it was a “daunting diagnosis.”
“There is no 'how-to manual' for raising a child with autism,” Johnston said.
Siblings Fraiser, left, Evie Jane and Carter Johnston swing as parents Brian and Laura Beth Johnston look on.
But with the support of therapists and specialists, Fraiser, now 5, started kindergarten this year. Johnston said she and her family also found support through a group for families affected by autism spectrum disorders (ASD).
“We met parents with the same fears and concerns,” Johnston said.
During one of those meetings, Johnston learned about a study at the University of Mississippi Medical Center's Center for Advancement of Youth (CAY) clinic that hopes a SPARK can shine light on ASD.
Dr. Robert Annett, professor of pediatrics, is leading the UMMC study site for the SPARK (Simons Foundation Powering Autism Research for Knowledge) national genetic study of ASD.
“SPARK's goal is to build a registry of genetic information from individuals with autism and their families,” Annett said. “The results will be important for identifying the causes of autism and informing treatment-related studies in the future.”
UMMC is one of 21 institutions that will recruit a combined 50,000 participants and families. This will be the largest ASD study ever undertaken and is sponsored by the Simons Foundation Autism Research Initiative
The UMMC SPARK team from left, research coordinator Kristen Callahan, Annett, research coordinator Sabrina White and assistant professor of pediatrics Dr. Dustin Sarver.
According to the Centers for Disease Control, one out of 68 children has ASD. However, Mississippi does not have a reliable estimate, said Annett, a pediatric neuropsychology specialist with experience with longitudinal cohort studies.
“There is a huge need in Mississippi to build an ASD cohort,” Annett said, to better understand and strengthen educational and health-care resources for individuals with ASD. SPARK may help make that happen.
SPARK is a genome-wide association study (GWAS). GWAS collects whole DNA sequences (genomes) from people who share a common trait, such as ASD. Researchers look for genetic markers, or gene variations that may contribute to ASD.
There are about 20 genetic marker “hotspots” connected to ASD, Annett said, but there are hundreds more that could also be important. However, scientists do not understand how the different markers influence a person's ASD symptoms, behaviors and traits.
“In people with autism spectrum disorders, there are differences in the rate and acquisition of learning, namely with social communication skills,” said Dr. Dustin Sarver, assistant professor of pediatrics and SPARK co-investigator. He studies learning and cognition in youth with attention deficit/hyperactivity disorder, which he says often co-occur with ASD.
The wide range of ASD characteristics and differences make it challenging to study potential causes or treatments, Annett said. By recruiting a large cohort, researchers can divide subjects into smaller, more similar groups to study.
Participating families pick up a DNA collection kit from the CAY clinic or receive it in the mail. Each family member spits or swabs their saliva into a tube and mails the sample to a laboratory where scientists test the extracted DNA for the genetic markers, a process called genotyping. They also answer medical history questions online. Families can receive their results after testing.
By collecting DNA from parents and siblings of children with ASD, researchers can study if and how children may inherit ASD.
“This project is about families, not just ASD individuals,” Annett said. “It is important for these families to have a seat at the table so that an individual's needs can be expressed.”
The SPARK registry will also become a resource for scientists conducting future studies on ASD. By participating, families may be recruited for related clinical trials or registries.
“The intent is to have a better understanding of the subtypes of autism,” Annett said. “With this genetic information, we may be able to predict how these subtypes respond to different therapies or medications.”
The UMMC CAY goal is to recruit 1500 families during the next three years. To reach that goal, they are collaborating with teams at Mississippi State University and the University of Southern Mississippi to conduct statewide outreach.
“Overall, families are very interested in the study,” said Sabrina White, a CAY research coordinator. She and Kristen Callahan, another research coordinator, work directly with families to answer their questions and prepare them to participate. They have been traveling to communities and summer camps across Mississippi to build relationships and recruit families for the study.
Johnston said she and her family decided to participate in SPARK because the study could help answer ASD's many unknowns. It could help answer her older son's questions as well.
Fraiser plays with his brother and sister at Strawberry Patch Park in Madison.
“Carter [Johnston's oldest son] will sometimes ask me why Fraiser has autism,” Johnston said. “Or Carter will ask why he and his younger sister don't have autism.
“We hope that someday other families with children with ASD won't face the challenges that we face,” she said.
Annett said that any new ASD therapies or treatments based on SPARK could be 10 to 15 years away. However, the research is an important step in that direction.
“Our ultimate goal is to improve the quality of life for people with ASD,” Annett said.
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