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Neuroimaging study reveals structural brain differences in children with autism - MSN News
Thursday, October 10, 2024
There is new evidence that the cells responsible for communication in the brain may be structured differently in children with autism. Researchers at the Del Monte Institute for Neuroscience at the University of Rochester discovered that in some areas of the brain neuron density varies in children with autism when compared to the general population.
“We are at the beginning of understanding the true impact that the extraordinary data collected by the ABCD Study will have on the health of our children,” says John Foxe, the Kilian J. and Caroline F. Schmitt Chair in Neuroscience and the director of the Del Monte Institute for Neuroscience and the Golisano Intellectual and Developmental Disabilities Institute. “It is truly transforming what we know about brain development as we follow this group of children from childhood into early adulthood.”
Read More: Neuroimaging study reveals structural brain differences in children with autism - MSN NewsResearch finds neurons look different in children with autism
Wednesday, October 9, 2024
Neuronal measurements may provide new insight into diagnosis & therapeutic interventions for autism
There is new evidence that the cells responsible for communication in the brain may be structured differently in children with autism. Researchers at the Del Monte Institute for Neuroscience at the University of Rochester discovered that in some areas of the brain neuron density varies in children with autism when compared to the general population.
“We've spent many years describing the larger characteristics of brain regions, such as thickness, volume, and curvature,” said Zachary Christensen, MD/PhD candidate at the University of Rochester School of Medicine and Dentistry, and first author of the paper out today in Autism Research. “However, newer techniques in the field of neuroimaging for characterizing cells using MRI, unveil new levels of complexity throughout development.”
Imaging provides new insight into brain development
Researchers used brain imaging data collected from more than 11,000 children ages 9-11. They compared the imaging of the 142 children in that group with autism, to the general population and found there was lower neuron density in regions of the cerebral cortex. Some of these regions of the brain are responsible for tasks like memory, learning, reasoning, and problem-solving. In contrast, the researchers also found other brain regions, such as the amygdala—an area responsible for emotions—that showed increased neuron density. In addition to comparing the scans of children with autism to those of children without any neurodevelopmental diagnosis, they also compared the children with autism to a large group of children diagnosed with common psychiatric disorders like ADHD and anxiety. The results were the same, suggesting that these differences are specific to Autism.
“People with a diagnosis of autism often have other things they have to deal with, such as anxiety, depression, and ADHD. But these findings mean we now have a new set of measurements that have shown unique promise in characterizing individuals with autism,” Christensen said. “If characterizing unique deviations in neuron structure in those with autism can be done reliably and with relative ease, that opens a lot of opportunities to characterize how autism develops, and these measures may be used to identify individuals with autism that could benefit from more specific therapeutic interventions.”
Read More: Research finds neurons look different in children with autismJohn Foxe spoke on Fairport Central School District making changes to school day schedule
Wednesday, September 18, 2024
John Foxe, PhD, director of the Del Monte Institute for Neuroscience, spoke to WHAM (Sept. 18) about Fairport School District altering start times for middle and high schoolers in 2026. "We have clear evidence from neurosciences that it’s at night when you’re sleeping that your memory systems consolidate the information you took in during the day," said Foxe. "What we will see is less falling asleep, less distraction, better behavior, more learning and ability to take on more material.”
Researchers find possible neuromarker for ‘juvenile-onset’ Batten disease
Monday, January 8, 2024
Early symptoms can be subtle. A child’s personality and behavior may change, and clumsiness or stumbling develops between the ages of five and ten. Over time, cognitive impairment sets in, seizures emerge or worsen, vision loss begins, and motor skills decline. This is the course of Batten disease, a progressive inherited disorder of the nervous system that results from mutations to the CLN3 gene.
“It is a devastating neurodegenerative disorder of childhood,” said John Foxe, PhD, director of the Del Monte Institute for Neuroscience and co-director of the University of Rochester Intellectual and Developmental Disabilities Research Center (UR-IDDRC), “and while it is very rare, it is important to study and understand because it could inform what we know and how we treat it and other related rare diseases.”
In a new study, out today in the Journal of Neurodevelopmental Disorders, Foxe and a team of researchers from the University of Rochester Medical Center may be closer to that goal of understanding. The paper describes how they measured changes in brain function of participants with CLN3 disease, also known as 'juvenile-onset' Batten disease. Researchers found that the functioning of the auditory sensory memory system—the brain system required for short-term memory recall—appears to decrease as the disease progresses. They revealed this by utilizing electroencephalographic recordings (EEG) to measure the brain activity of participants with and without Batten disease as they passively listened to simple auditory beeps. The participants simultaneously watched a video of their favorite movie while the brain responses to these beeps were being measured. In the participants with Batten disease, the EEG revealed a decline in the response from the auditory sensory memory system as the disease progressed. There were no significant changes among the other participants. This finding suggests that this easy-to-measure brain process may be a target or biomarker in measuring treatment outcomes in clinical trials.
“We needed to find a task that did not require explicit engagement or attention, and this is one of those kinds of tasks,” Foxe said. “The brain produces the signal that we're looking at, regardless of whether the participant is paying attention to the beeps or not. It is an objective method that provides new insight into the brain function of a population with varying communication abilities.”
Read More: Researchers find possible neuromarker for ‘juvenile-onset’ Batten disease