Autism spectrum disorder is a neurological and developmental condition. The condition affects how people interact, communicate, learn, and behave with others.
Research from the UC Davis MIND Institute sheds light on maternal autoantibody-related autism
A neurodevelopmental condition called autism spectrum disorder affects 1 in 44 kids in the United States. It has a broad range of characteristics with various intensities and origins. Maternal autoantibody-related autism spectrum disorder (MAR ASD) is one kind of autism.
The presence of certain maternal immune proteins known as autoantibodies that respond to certain proteins identified in the fetal brain characterizes MAR ASD. Maternal autoantibodies (IgG) pass the placenta and enter the developing brain. Once there, they may alter the way the brain develops in children, resulting in autism-like symptoms.
Two new UC Davis MIND Institute studies are helping us learn more about this kind of autism. They discovered evidence for predictive protein patterns in the blood of pregnant women, as well as correlations between MAR ASD and greater intensities of autistic symptoms.
MAR ASD patterns linked to autism before birth
The MIND Institute’s Judy Van de Water and a team of researchers showed that autoantibody binding to nine specific combinations of proteins (known as MAR ASD patterns) successfully predicts autism in previously diagnosed children. They tested maternal blood samples collected during pregnancy to see if they could validate the identified patterns. They wanted to see if the patterns accurately predicted autism in the children. Their study findings were recently published in the journal Molecular Psychiatry.
Judy Van de Water, UC Davis professor of immunology and neurodevelopment, and senior author of the study.
“Previously, we identified nine patterns linked to MAR ASD. In this study, we wanted to check the accuracy of these patterns in predicting MAR ASD. To do that, we tested plasma from pregnant mothers, collected by the Early Markers for Autism (EMA) study,” said Van de Water, the study’s senior author. Van de Water is a UC Davis professor of immunology and neurodevelopment.
The study screened the plasma of 540 mothers of autistic children, 184 mothers of kids with intellectual disability but no autism, and 420 general population mothers of kids with no known autism or intellectual disability at the time of the study.
It found reactivity to at least one of the nine MAR ASD patterns in 10% of the autistic group. This is compared with 4% of the intellectual disability group for some patterns, and 1% of the general population group. Four patterns were present only in mothers whose children were later diagnosed with autism, making those particular autoantibody patterns highly predictive.
The study also found that a mother with reactivity to any one of the nine MAR ASD patterns has around 8 times the chance of having an autistic child.
Several MAR ASD patterns were strongly associated with autism with intellectual disability. Others were linked to autism without intellectual disability. The protein pattern most strongly linked to autism was (CRMP1+CRMP2). It increased the likelihood of an autism diagnosis by 16 times and was not found in the non-autism groups.
MAR ASD similarly present across states
Previous research found the MAR subtype of autism in 20% of a Northern California sample of autistic kids Yet, until now, this type of autism has not been studied in any state besides California.
A team of researchers led by Kathleen Angkustsiri explored MAR ASD in two new clinical sites: the Children’s Hospital of Philadelphia (CHOP) and Arkansas Children’s Hospital and Research Institute (ACHRI). Their study, published in The Journal of Developmental and Behavioral Pediatrics, recruited 68 mothers of autistic children ages 2-12 years. The mothers provided blood samples and completed behavioral questionnaires about their children.
Early diagnosis allows for customized child support. Credit: University of California – Davis Health
The study also included data from the children’s clinical diagnostic assessments. It used established diagnostic measures known as ADOS (the autism diagnostic observation schedule) and Social Communication Questionnaire (SCQ) to assess the children’s autistic characteristics.
MAR ASD was present in 21% of CHOP’s and 26% of ACHRI’s samples. Overall, 23.5% of the blood samples were considered MAR positive (+MAR), showing autoantibodies reacting to known MAR ASD protein patterns.
“Our study showed similar MAR ASD frequencies in two other states similar to what we observed in Northern California,” Angkustsiri said. Angkustsiri is an associate professor of developmental-behavioral pediatrics at UC Davis Children’s Hospital and the UC Davis MIND Institute and the study’s lead author. “This suggests that the prevalence of MAR ASD is consistent across different demographics and geographic settings.”
MAR ASD and autism characteristics
The study also examined the link between MAR ASD and autism severity. It showed that children of mothers with +MAR antibodies had higher autism severity scores than those of -MAR mothers. It did not find significant differences in their IQ, adaptive function, or unusual behavior.
“MAR ASD positivity may be linked to more severe autism behaviors,” Angkustsiri said. “Both the SCQ reported by parents and the ADOS assessed by clinicians supported these findings.”
Further study is needed to understand why mothers develop these antibodies and how long these antibodies may persist. Testing for MAR ASD patterns can be used to assess the probability of a child having autism before characteristics are present. The researchers aim to develop an accurate clinical test to provide clinicians with more tools for an earlier diagnosis of ASD.
“We hope our work can help develop better-tailored services based on the type of autism and the child’s strengths and specific challenges,” Van de Water said.
The study was funded by the NIH/National Institute of Environmental Health Sciences, the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the Consejo Nacional de Ciencia y Tecnologia, and the DBPNet Young Investigator Award.
References: “Maternal autoantibody profiles as biomarkers for ASD and ASD with co-occurring intellectual disability” by Alexandra Ramirez-Celis, Lisa A. Croen, Cathleen K. Yoshida, Stacey E. Alexeeff, Joseph Schauer, Robert H. Yolken, Paul Ashwood, and Judy Van de Water, 26 May 2022, Molecular Psychiatry.
DOI: 10.1038/s41380-022-01633-4
“Pilot Study of Maternal Autoantibody–Related Autism” by Angkustsiri, Kathleen MD, MAS, Fussell, Jill J. MD, Bennett, Amanda MD, MPH, Schauer, Joseph BS, Ramirez-Celis, Alexandra Ph.D., Hansen, Robin L. MD and Van de Water, Judy Ph.D., 1 June 2022, Journal of Developmental and Behavioral Pediatrics.
DOI: 10.1097/DBP.0000000000001100
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