A new UC San Francisco (UCSF) study that mapped the neural connections of newborns with two different kinds of brain injuries found the maps looked very different – and were linked to significantly different developmental outcomes years later. An article detailing the research appears on the UCSF website.

By Jess Berthold, Senior Public Information Representative, UCSF

The study, published January 5 in PLoS ONE and led by UCSF pediatrics, neurology, and radiology researchers, used diffusion MRI to visualize the brain wiring of two sets of newborns: one set with congenital heart defects (CHD) and the other with hypoxic-ischemic encephalopathy (HIE) – otherwise known as birth asphyxia.

HIE babies suffer brain injury and oxygen deprivation within days to hours of being born, while CHD babies are steadily deprived of oxygen for longer – often months – in utero.  Both groups are known to be at high risk for neurodevelopmental disabilities as they grow older, in areas ranging from motor skills to attention to behavioral issues.

“You have two sets of kids who, before or during birth, have a brain injury and then end up having some delayed or altered development and problems at school age,” said Patrick McQuillen, MD, UCSF professor of pediatrics and neurology, and the study’s corresponding author. “We wondered if the newborn brain, when faced with something challenging at different times, responds in the same way. What we found was the brains of these two sets of babies looked very, very different.”

Brain Differences Linked to Outcomes

The researchers found that the distinct differences in brain wiring between the groups correlated with motor and language outcomes later. Specifically, they found the CHD newborns had worse language function at 12 to 18 months and worse cognitive, language, and motor function at 30 months than the infants born with HIE, whose outcomes at both time points were in the normal range.

While about 20% of CHD babies scored below the normal language range at 12-18 months, the number grew to 50% below normal by 30 months. In addition, 37% of CHD children scored below normal in the cognitive domain and 25% scored below normal in the motor domain at 30 months. Language delays appeared to be driven by expressive, not receptive, language deficiencies, the study authors noted.

The main difference between the CHD and HIE brains that showed up in imaging was in an area called “global efficiency,” which measures how easy it is for a connection to be made from one area of the brain to the other. An efficient brain resembles a traffic system with an ideal balance of highways and local roads that take a driver where she needs to go quickly, McQuillen explained.

The researchers will continue to follow the babies in the study and were recently awarded a grant from The Children’s Heart Foundation to conduct additional brain imaging and testing of the subjects at school age. Their hope is that by understanding how the brain connections work and match to developmental outcomes, researchers will be able to link children with brain injuries to early intervention more quickly. Eventually, children may even have treatments tailored to their type of brain injury.

“We’re not quite there yet,” McQuillen said. “We are still in the stage of describing what’s different, and using those patterns to make predictions about outcomes. But I am hopeful about where this is headed.”

Co-Authors: Additional authors on the study include Shabnam Peyvandi, MD, MAS, and Stephany Cox, PhD, from the UCSF Department of Pediatrics; Dawn Gano, MD, MAS, from the UCSF Departments of Pediatrics and Neurology; Duan Xu, PhD, and Olga Tymofiyeva, PhD, from the UCSF Department of Radiology. Alice Ramirez, MD, was a UCSF critical care fellow at the time this research was conducted.

Funding: This study was supported by NIH grants P01NS082330 and K23NS099422.

Original Paper: Ramirez A, Peyvandi S, Cox S, et al. Neonatal brain injury influences structural connectivity and childhood functional outcomes. PLoS ONE. 2022;17(1):e0262310.

Source: UCSF, PLoS ONE