A new study published in Molecular Psychiatry has provided groundbreaking insights into the biological underpinnings of autism, revealing that adults with autism have fewer synapses in their brains than neurotypical individuals. Using a type of brain imaging called positron emission tomography, researchers measured synaptic density directly in living individuals for the first time. They discovered a strong link between reduced synaptic density and difficulties in social interaction and communication, offering a potential explanation for some of the challenges faced by autistic people.
Autism spectrum disorder is a complex condition that affects communication, behavior, and social interaction. Although it is well established that genetic and environmental factors play roles in autism, the biological mechanisms behind its features remain unclear. Many researchers have speculated that synapses, the connections that allow brain cells to communicate, are altered in autism. Previous studies have suggested this possibility based on animal models and post-mortem brain tissue, but these methods provide only indirect evidence.
To address this gap, the research team at Yale School of Medicine aimed to directly measure synaptic density in living individuals with autism. They hoped to uncover whether reduced synapses might be a factor in the social and communicative challenges experienced by autistic people, as well as to explore how these changes might inform future therapeutic approaches.
The study involved 32 adults between the ages of 18 and 35. Of these, 12 were autistic, and 20 were neurotypical. The two groups were matched for age and gender, ensuring comparability. All participants underwent extensive health and psychological screening, with autistic participants meeting rigorous diagnostic criteria through clinical evaluation and standardized assessments. To ensure the validity of the findings, participants with other medical or psychiatric conditions, a history of substance abuse, or current use of medications affecting synaptic density were excluded.
The researchers utilized an advanced form of positron emission tomography featuring a radioactive tracer, 11C-UCB-J, developed in collaboration with the Yale PET Center. This tracer binds to a protein uniquely located in synaptic vesicles, enabling precise quantification of synapses across different brain regions. To complement the positron emission tomography scans, participants also underwent magnetic resonance imaging, ensuring accurate mapping of the collected data. Each imaging session lasted approximately 90 minutes, during which detailed information on synaptic density was gathered and analyzed.
The findings revealed a consistent pattern: adults with autism had fewer synapses throughout their brains compared to neurotypical individuals. On average, synaptic density was about 10% lower in the autistic group, with particularly pronounced differences in regions known to be important for social and cognitive functions, such as the parietal cortex.
One of the most striking discoveries was the strong correlation between synaptic density and social-communicative function. Participants with fewer synapses were more likely to exhibit greater difficulties in social interaction and communication, as measured by clinical assessments. These relationships were observed across the entire brain, not limited to regions traditionally associated with social behavior. This suggests that the challenges faced by autistic individuals might stem from widespread differences in how their brains process and transmit information.
The findings align with previous research indicating that genetic and developmental factors affecting synaptic plasticity may play a role in autism. However, this study is unique in its ability to directly measure synapses in living individuals, providing the first clear evidence of reduced synaptic density as a characteristic feature of autism.
“As simple as our findings sound, this is something that has eluded our field for the past 80 years,” said James McPartland, the Harris Professor of Child Psychiatry and Psychology at the Yale Child Study Center and the study’s principal investigator. “And this is truly remarkable—because it’s very unusual to see correlations between brain differences and behavior this strong in a condition as complex and heterogeneous as autism.”
Despite its groundbreaking nature, the study has some limitations. The sample size, while typical for a study involving positron emission tomography, was relatively small, and the findings need to be replicated in larger and more diverse groups. Additionally, all participants were adults, meaning the study could not address how synaptic density might change over the course of development. Future research will need to explore these changes in younger individuals to determine whether reduced synaptic density is a cause of autism or a result of living with the condition.
This research marks a significant step forward in understanding the biology of autism. By identifying synaptic differences as a key feature of the condition, the findings offer a potential pathway for developing new interventions. For instance, therapies aimed at improving synaptic function might help alleviate some of the social and communicative challenges faced by autistic individuals.
The researchers are already exploring less invasive and more affordable imaging methods that could make it easier to study these brain differences in larger and younger populations. They are also investigating how reduced synaptic density might relate to other challenges commonly associated with autism, such as heightened risks for anxiety and depression. “This is something that’s really important for us to investigate to serve our overarching goal, which is to get information that can maximize the quality of life for autistic people,” McPartland explained.
The study, “11C-UCB-J PET imaging is consistent with lower synaptic density in autistic adults,” was authored by David Matuskey, Yanghong Yang, Mika Naganawa, Sheida Koohsari, Takuya Toyonaga, Paul Gravel, Brian Pittman, Kristen Torres, Lauren Pisani, Caroline Finn, Sophie Cramer-Benjamin, Nicole Herman, Lindsey H. Rosenthal, Cassandra J. Franke, Bridget M. Walicki, Irina Esterlis, Patrick Skosnik, Rajiv Radhakrishnan, Julie M. Wolf, Nabeel Nabulsi, Jim Ropchan, Yiyun Huang, Richard E. Carson, Adam J. Naples, and James C. McPartland.
