Summary:Researchers report early indicators of depression and anxiety may be evident in the brain from birth.
Brain scans may indicate clues to later problems.
Early predictors of anxiety and depression may be evident in the brain even at birth, suggests a study at Washington University School of Medicine in St. Louis.
Analyzing brain scans of newborns, the researchers found that the strength and pattern of connections between certain brain regions predicted the likelihood of the babies developing excessive sadness, shyness, nervousness or separation anxiety by age 2. Such symptoms have been linked to clinical depression and anxiety disorders in older children and adults.
The research is published online in the Journal of the American Academy of Child & Adolescent Psychiatry.
“The fact that we could see these connectivity patterns in the brain at birth helps answer a critical question about whether they could be responsible for early symptoms linked to depression and anxiety or whether these symptoms lead to changes in the brain,” said Cynthia Rogers, MD, an assistant professor of child psychiatry. “We have found that already at birth, brain connections may be responsible for the development of problems later in life.”
Initially, Rogers and her team set out to identify differences in functional brain connectivity — the coordination of activity across different parts of the brain — between babies born prematurely and others born at full term. They conducted functional MRI scans in 65 full-term newborns and 57 premature infants born at least 10 weeks early. The latter were scanned on or near their due dates.
The researchers looked for differences in the connectivity patterns across various regions of the brain, hoping to find evidence to explain why premature babies face a greater risk of developing psychiatric problems — including depression and anxiety — later in life. In particular, the team focused on how a structure involved in the processing of emotions, called the amygdala, connects with other brain regions.
First, they found that healthy, full-term babies had patterns of connectivity between the amygdala and other regions of the brain that were similar to the patterns previous studies had indicated in adults. Although there were similar patterns of connectivity in premature infants, the strength of their connections between the amygdala and other brain regions was decreased.
Most interestingly, they noted that various connection patterns between the amygdala and other structures — like the insula, which is involved in consciousness and emotion, and the medial prefrontal cortex, which plays roles in planning and decision making — appear to increase the risk of early symptoms related to depression and anxiety.
When the babies turned 2 years old, a subset received follow-up assessments to look for early symptoms of anxiety and depression. The researchers evaluated 27 of the children who were born prematurely and 17 born at term.
“Children born prematurely were no more likely than full-term children to exhibit early signs of anxiety and depression,” Rogers said. “Part of that may have been due to the fact that a number of the full-term children already were at risk for symptoms due to sociodemographic factors, such as living in poverty or having a mother with clinical depression or an anxiety disorder. Further, the severity of these early anxiety symptoms was correlated with connectivity patterns seen in the infants in both groups.”
The researchers also want to evaluate all children from the study again when they are 9 to 10 years old to learn whether brain connections continue to influence the risk for depression and anxiety disorders.
“We have a grant under review to bring the preterm children back when they are older, along with the full-term children, and we want to study how their brains have developed over time,” Rogers said. “We want to determine whether they still have many of the same differences in connectivity, whether there have been any changes in the structural and functional connections in their brains, and how all of that relates to whether they have symptoms of psychiatric disorders.”
Funding: This work was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the National Institute of Mental Health and the National Institute of Neurological Disorders and Stroke of the National Institutes of Health (NIH), grant numbers R01 HD061619, UL1 TR000448, KL2 TR000250, K23 MH105179, K02 NS0898521 and P30 HD062171. Additional funding was provided by the McDonnell Center for Systems Neuroscience, the Intellectual and Developmental Disabilities Research Center at Washington University, the Child Neurology Foundation, the Cerebral Palsy International Research Foundation, the Dana Foundation and the Doris Duke Foundation.
Source: Jim Dryden – WUSTL
Image Source: NeuroscienceNews.com image is credited to WUSTL.
Original Research: Abstract for “Neonatal Amygdala Functional Connectivity at Rest in Healthy and Preterm Infants and Early Internalizing Symptoms” by Cynthia E. Rogers, MD, Chad M. Sylvester, MD, PhD, Carrie Mintz, MD, Jeanette K. Kenley, BS, Joshua S. Shimony, MD, PhD, Deanna M. Barch, PhD, Christopher D. Smyser, MD in Journal of the American Academy of Child & Adolescent Psychiatry. Published online November 25 2016 doi:10.1016/j.jaac.2016.11.005
Neonatal Amygdala Functional Connectivity at Rest in Healthy and Preterm Infants and Early Internalizing Symptoms
Alterations in the normal developmental trajectory of amygdala resting state functional connectivity (rs-FC) have been associated with atypical emotional processes and psychopathology. Little is known, however, regarding amygdala rs-FC at birth or its relevance to outcomes. This study examined amygdala rs-FC in healthy, full-term (FT) infants and in very preterm (VPT) infants, and tested whether variability of neonatal amygdala rs-FC predicted internalizing symptoms at age 2 years.
Resting state fMRI data were obtained shortly after birth from 65 FT infants (gestational age [GA] ≥36 weeks) and 57 VPT infants (GA <30 weeks) at term equivalent. Voxelwise correlation analyses were performed using individual-specific bilateral amygdala regions of interest. Total internalizing symptoms and the behavioral inhibition, depression/withdrawal, general anxiety, and separation distress subdomains were assessed in a subset (n = 44) at age 2 years using the Infant Toddler Social Emotional Assessment. Results
In FT and VPT infants, the amygdala demonstrated positive correlations with subcortical and limbic structures and negative correlations with cortical regions, although magnitudes were decreased in VPT infants. Neonatal amygdala rs-FC predicted internalizing symptoms at age 2 years with regional specificity consistent with known pathophysiology in older populations: connectivity with the anterior insula related to depressive symptoms, with the dorsal anterior cingulate related to generalized anxiety, and with the medial prefrontal cortex related to behavioral inhibition.
Amygdala rs-FC is well established in neonates. Variability in regional neonatal amygdala rs-FC predicted internalizing symptoms at 2 years, suggesting that risk for internalizing symptoms may be established in neonatal amygdala functional connectivity patterns.
“Neonatal Amygdala Functional Connectivity at Rest in Healthy and Preterm Infants and Early Internalizing Symptoms” by Cynthia E. Rogers, MD, Chad M. Sylvester, MD, PhD, Carrie Mintz, MD, Jeanette K. Kenley, BS, Joshua S. Shimony, MD, PhD, Deanna M. Barch, PhD, Christopher D. Smyser, MD in Journal of the American Academy of Child & Adolescent Psychiatry. Published online November 25 2016 doi:10.1016/j.jaac.2016.11.005