Research shows science getting closer to reduce seizures, sleep disturbances in intellectually disabled

Research led by a team of UNLV neuroscientists has shown the potential to zero in on the root-level cause of a host of adverse symptoms associated with unique subtypes of neurodevelopmental disorders, work that could one day improve the lives of millions worldwide. 

The study was published in the 'Nature' journal, 'Molecular Psychiatry'. It built on previous research by UNLV neuroscientist Rochelle Hines and collaborators, which discovered that two key proteins -- collybistin and the GABAA receptor a2 subunit -- controlled the firing of brain cells and contributed to epileptic seizures, learning and memory deficiencies, sleep disturbances, and other symptoms frequently associated with various forms of intellectual disability including Down syndrome, autism, and ADHD.

The team's newest findings unveiled that mutations in ARHGEF9 -- the gene that codes for collybistin -- lead to intellectual disability through impaired a2 subunit function. 

The team further showed that a2 was a central hub for many of the adverse neurological symptoms characteristic of multiple intellectual disability subtypes. 

"Seizures and sleep deficits are two of the most common and most disruptive symptoms in children with neurodevelopmental disorders, and sleep deficits in particular are not well treated and can impact the entire family," said Hines, who partnered with UNLV faculty and undergraduate and graduate student researchers, as well as scientists from Tufts University and Boston Children's Hospital. 

"This research gives new hope to patients that we can now develop drug therapies and provide more precise interventions."

In addition to patients with neurodevelopmental disorders, researchers said their study had the potential to improve the quality of life more broadly for people who grapple with sleep dysfunction, epilepsy, anxiety, hyperactivity, and other neurological abnormalities.