1. Neuroscience
  2. Medicine

Study reveals greater excitability in social brain regions of autistic men compared to women

New findings suggest that autistic men, but not women, have enhanced neural excitability in their social brain regions, and this may impact their ability to navigate social situations.
Press Pack
  • Views 108
  • Annotations

New insight on differences in the brains of men and women with autism has been published today in the open-access journal eLife.

The study suggests that autistic men, but not women, have enhanced neural excitability in specific brain regions that are important for social cognition and self-reflection, and this may differentially impact their ability to navigate social situations.

These findings support the idea that imbalances between excitation and inhibition in the brain affect some individuals with autism more than others. They also pave the way for further research to measure the imbalance of excitation and inhibition with non-invasive neuroimaging techniques. This could help scientists evaluate how different treatments may affect this aspect of the brain’s biology.

The brain possesses its own natural balance between excitation and inhibition, but this balance differs among individuals. Higher levels of excitation are linked to the function of some autism-relevant genes that are found on the sex chromosomes, and can also be affected by hormones produced in higher quantities in men, such as testosterone. Differences in these sex-related mechanisms are important as autism affects males more than females.

“With this study, we wanted to gain a better understanding of how excitation-inhibition imbalance may affect autistic men differently to women,” says one of the study’s lead authors, Stavros Trakoshis, a graduate student at the Laboratory for Autism and Neurodevelopmental Disorders at the Istituto Italiano di Tecnologia (IIT) in Rovereto, Italy, and also based at the University of Cyprus.

To do this, Trakoshis and his colleagues started by using a computer model that simulates excitatory and inhibitory neurons as they interact and influence each other within the brain. The model allowed them to control the ratio of mixture between excitation and inhibition, simulated these interactions, and then reported neuronal population responses over time. The outputs are similar to data commonly measured with neuroimaging techniques, such as electroencephalography (EEG) and functional magnetic resonance imaging (fMRI).

Trakoshis and the team observed that specific statistical attributes of the simulated data changed systematically with changes to the underlying excitation-inhibition ratios. These statistical changes were also validated using data from fMRI scans of brains in living mice that were given drugs to induce enhanced excitation.

After validating that non-invasive fMRI can reveal changes to the underlying cellular excitation-inhibition ratio, the team next applied their technique to fMRI data from adult men and women with autism. This revealed that autistic men, but not women, have atypically enhanced excitation in a brain region called the medial prefrontal cortex. The function of this brain region is typically associated with social cognition and self-reflection. The analysis also showed that, in women with autism, a more intact medial prefrontal cortex response (with less enhanced excitation, for example) was associated with better camouflaging of social difficulties in real-world social situations.

“Our work suggests that sex-related biological mechanisms could be integral for how excitation-inhibition balance develops in autistic men versus women,” says senior author Michael Lombardo, Director of the Laboratory for Autism and Neurodevelopmental Disorders at the IIT. “This could help explain why we see phenomena such as camouflaging manifesting differently in autistic males versus females.

“Our approach could also be useful for understanding other neurodevelopmental conditions that affect males more than females, such as attention deficit-hyperactivity disorder,” Lombardo concludes.

Media contacts

  1. Emily Packer
    eLife
    e.packer@elifesciences.org
    +441223855373

About

eLife is a non-profit organisation created by funders and led by researchers. Our mission is to accelerate discovery by operating a platform for research communication that encourages and recognises the most responsible behaviours. We work across three major areas: publishing, technology and research culture. We aim to publish work of the highest standards and importance in all areas of biology and medicine, including Human Biology and Medicine and Neuroscience, while exploring creative new ways to improve how research is assessed and published. We also invest in open-source technology innovation to modernise the infrastructure for science publishing and improve online tools for sharing, using and interacting with new results. eLife receives financial support and strategic guidance from the Howard Hughes Medical Institute, the Knut and Alice Wallenberg Foundation, the Max Planck Society and Wellcome. Learn more at https://elifesciences.org/about.

To read the latest Human Biology and Medicine research published in eLife, visit https://elifesciences.org/subjects/human-biology-medicine.

And for the latest in Neuroscience, see https://elifesciences.org/subjects/neuroscience.