Subgrouping mouse models of autism by brain structure or connectivity can reveal other commonalities among people who have the condition, according to two new unpublished studies. Researchers presented the findings last week at Neuroscience 2022 in San Diego, California.
Autism’s heterogeneity complicates its study. Biomarkers evident within one subgroup may be diluted across the broader autistic population, for example. And clinical trials that succeed for one group can fail if they don’t work for the majority, says Jacob Ellegood, a research associate at the Mouse Imaging Centre in Toronto, Canada, who presented findings at the conference.
That challenge makes the identification of autism subgroups — sets of people who may respond similarly to treatments, for example — an appealing goal, he says. And how brain structure compares across different mouse models of autism offers one way to search for such subtypes.
In new work presented on 13 November, Ellegood and his colleagues linked nine mouse models of rare genetic conditions to better-known forms of autism, based on neuroanatomy. Similar pathways may underlie these different genetic conditions, Ellegood says.
Another team at last week’s conference sorted 19 autism mouse models into two groups according to functional connectivity, a measure of synchronous activity across brain regions. Similar groups, the unpublished study shows, exist among people with idiopathic autism.
“There isn’t a single signature of autism in the brain,” says study investigator Marco Pagani, a research fellow at the Italian Institute of Technology in Roverto, Italy, and the Child Mind Institute in New York City, who presented the connectivity work on 16 November. (Pagani described his findings in a video for Spectrum.)
Pagani and his colleagues collected resting-state functional MRI scans in 10 to 20 mice for each of their 19 models.
Compared with wildtype mice, the autism model mice showed either an overall increase in functional connectivity, including mice with a mutation in the gene CHD8 or TSC2; or a decrease, including those with a mutation in SHANK3 or in chromosomal regions 16p11.2 or 22q11.2.
In both subtypes, the striatum showed atypical connectivity, Pagani and his colleagues discovered when they examined how the functional connectivity patterns were distributed across the brain. The overconnected subtype also showed altered functional connectivity in the amygdala and hippocampus, whereas the underconnected subgroup showed altered functional connectivity in cortical regions. And those patterns mapped to those seen in the brains of some people with idiopathic autism, based on an analysis using the Autism Brain Imaging Data Exchange (ABIDE) datasets.
Pagani and his colleagues identified 166 autistic participants with the hyperconnected brain signature and 79 with the under-connected signature.
Participants within each group had similar overall scores on measures of restricted and repetitive behaviors, according to the Autism Diagnostic Observation Schedule. But people with hyperconnectivity had significantly higher scores — indicating more severe difficulties — on the social affective component.
Autism-linked genes were more highly expressed in brain areas that have atypical connectivity, an analysis of postmortem brain tissue from autistic people revealed, suggesting that these genes might hold clues about the biology behind the different subtypes, Pagani says.
Ellegood and his colleagues performed structural MRI scans of 150 different mouse models of autism, evaluating how different regions of the animals’ brains vary in volume. Then they clustered the models, including the nine new ones, into groups with similar neuroanatomy, using an algorithm that considers both the relative and absolute volume of each brain region.
“The main goal is to not necessarily fully categorize autism, but at least link models together that wouldn’t otherwise be linked together,” Ellegood says.
The clusters revealed relationships across autism-linked genes. For example, mice with mutations in the gene YPEL2, which is also called DiGeorge syndrome-related protein, had neuroanatomy similar to that of mice with a deletion of the 22q11.2 chromosomal region, which model DiGeorge syndrome.
Ellegood and his colleagues aim to continue scanning the brains of every mouse model of autism.
And they are performing a similar analysis on structural brain scans from people with idiopathic autism, with the goal of matching participants’ scans to the previously identified mouse clusters. That could help point to molecular pathways that contribute to different forms of idiopathic autism, he says.
Ellegood and Pagani also plan to compare their results to see if they can spot any overlap among their different subgroups. But they may be picking up on different signals, Pagani says.
“Any way that you can refine this heterogeneity is powerful,” Ellegood says. “And hopefully it’ll tell you something.”
Read more reports from Neuroscience 2022.
Cite this article: https://doi.org/10.53053/AOPK5363