Public Release: 

Brain changes linked to prematurity may explain risk of neurodevelopmental disorders

Children's Hospital Los Angeles

Disturbances in the early stages of brain growth, such as preterm birth - when many of the brain's structures have not yet fully developed - appears to affect the brain's neuro-circuitry, which may explain premature babies' higher risk of neurodevelopmental disorders including ADHD and autism spectrum disorder.

Researchers led by Natasha Lepore, PhD, of The Saban Research Institute of Children's Hospital Los Angeles, have located significant alterations to specific surface regions of the brain. Described in a study published online this week by the journal Brain Structure and Function, their identification of neuroanatomical changes related to prematurity helps explain what brain structure and circuitry are affected, and may lead to designing effective prevention strategies and early interventional treatments for cognitive disabilities.

Using three-dimensional brain structural magnetic resonance imaging (MRI), Lepore and colleagues analyzed the structure and neural circuitry of two specific areas of the brain in 17 preterm and 19 term-born babies: the thalamus - the brain's relay station, critical to sending and receiving sensory information - and the putamen, part of an intricate circuit connecting to the brain's frontal lobe and involved in a number of different processes, most notably regulation of movement and learning.

While many studies have spotted alterations in various brain structures related to prematurity, this is the first study to link the structural abnormalities to specific neuro-circuitry, the communication pathways of the brain. To investigate these changes, the CHLA researchers performed a novel, combined analysis of the external shape and dimension of the surfaces of the thalamus and putamen, and compared the relative position of these structures to one another.

"We found that regional abnormalities of the thalamus are associated with alterations of the putamen, possibly due to disturbed development of shared frontal-subcortical connectivity," said first author Yi Lao, MS, of the Department of Radiology at CHLA. More specifically, she added, the significantly correlated regions in these two structures point to frontal and sub-cortical pathways that are essential to important functions such as attention, decision-making, planning, abstract reasoning and memory.

Lepore adds that, for the first time, they have demonstrated the feasibility of using measurements of these abnormalities in the brain of preterm newborns as potential indicators of risk for future cognitive and behavioral problems.

"The ability to identify structural signs of neurodevelopmental disease shortly after birth in premature infants could allow for early interventions, increasing the child's social and learning behaviors as they age," said Lepore.

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Additional contributors include Yalin Wang, PhD, and Jie Shi, MS, Arizona State University; Rafael Ceschin, MS, Children's Hospital of Pittsburgh; Ashok Panigrahy, MD, Children's Hospital Los Angeles and Children's Hospital of Pittsburgh; and Marvin D. Nelson, MD, Children's Hospital Los Angeles. This work was supported by the National Institutes of Health through NIH grant 5K23-NS063371 and grants R21EB012177 and R21AG043760.

About Children's Hospital Los Angeles

Children's Hospital Los Angeles has been named the best children's hospital on the West Coast and among the top five in the nation for clinical excellence with its selection to the prestigious U.S. News & World Report Honor Roll. Children's Hospital is home to The Saban Research Institute, one of the largest and most productive pediatric research facilities in the United States. Children's Hospital is also one of America's premier teaching hospitals through its affiliation since 1932 with the Keck School of Medicine of the University of Southern California.

For more information, visit CHLA.org and follow us on ResearCHLAblog.org.

Media contact:

Debra Kain, dkain@chla.usc.edu
323-361-7628 or 323-361-1812

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