Summary: A new study confirms previous findings that link inflammation during pregnancy to altered brain development in children. Researchers have created a machine learning algorithm that can predict the long term neurodevelopmental impact of MIA.
Source: Oregon Health and Science University.
Inflammation is a normal part of the body’s response to infection, chronic stress or obesity. In pregnant women, it is believed that heightened inflammation increases the risk of mental illness or brain development problems in children.
A study conducted by researchers at OHSU in Portland, Oregon, has established a link between inflammation in pregnant women and the way the newborn brain is organized into networks. The results, published today in Nature Neuroscience, may provide promising avenues to explore treatments with potential to change these negative impacts on newborn brain function.
The research team, led by Damien Fair, P.A.-C., Ph.D., associate professor of behavioral neuroscience and psychiatry in the OHSU School of Medicine, and Claudia Buss, Ph.D., professor at the Charité – Universitätsmedizin Berlin, Berlin, Germany and associate professor at University of California Irvine, collected blood samples from 84 expectant mothers at each pregnancy trimester. The samples were measured for levels of the cytokine interleukin-6, or IL-6, an inflammatory marker known to play a role in fetal brain development.
Four weeks following birth, brain connectivity patterns of the offspring were assessed using functional magnetic resonance imaging, or fMRI, scans. At age 2, the children were also tested for working memory performance, a key skill that supports academic achievement and is frequently compromised in mental health disorders.
The data from mother and child show that differences in the levels of inflammatory markers are directly associated with differences in newborn brain communication, and later to working memory scores at age 2. Higher levels of the marker during pregnancy tended to result in less working memory capacity in the child.
“Importantly, this doesn’t mean that every exposure to inflammation will result in a negative impact to the child; however, these findings provide new avenues for research, and can help health care providers think about how, and when, inflammation might impact a child’s long-term learning development and mental health,” said Alice Graham, Ph.D., postdoctoral fellow in behavioral neuroscience in the OHSU School of Medicine.
A notable aspect of the study, according to Graham, is the development of a model that can accurately estimate information about maternal inflammation during pregnancy based only on newborn brain functioning. Created using artificial intelligence known as machine-learning, the model is based on the biomarkers identified in the study and can be applied to cases beyond the initial research group.
“Now, we have an approach that can utilize MRI brain scans of a newborn to accurately estimate the mother’s overall levels of inflammation during the time of her pregnancy,” she said. “This understanding provides some information about future memory function of that child approximately two-years later, creating a potential opportunity for research surrounding early clinical intervention, if necessary.”
In the future, Fair believes that research should focus on how factors before and after birth – such as society and environment – interact to influence the impacts to brain function and cognition in newborns.
“Increased stress and poor diet are considered normal by today’s standards, but greatly impact inflammation rates in all humans, not just expectant mothers,” he said. “Just as important to understanding how the immune system and inflammation affect early brain development, we also need to understand what common factors contribute to heightened inflammation so that we may target therapies to help reduce the rates of inflammation and overall impact on the developing brain.”
This study was completed in collaboration with University of California, Irvine. Marc Rudolph, a former research assistant in the OHSU School of Medicine, and current doctoral student in Cognitive Psychology at the University of North Carolina at Chapel Hill, is the study’s lead author.
Funding: Funding was provided by the Bill & Melinda Gates Foundation, The Destefano Innovation Fund, National Institutes of Mental Health (grants MH091351 and MH091351), National Center for Advancing Translational Sciences (award UL1TR0002369) and the National Institutes of Health (grants MH096773 and MH091238). Additional support was provided by the Oregon Clinical and Translational Research Institute, and the National Library of Medicine Postdoctoral Fellowship.
The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Source: Tracy Brawley – Oregon Health and Science University
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Abstract for “Maternal IL-6 during pregnancy can be estimated from newborn brain connectivity and predicts future working memory in offspring” by Marc D. Rudolph, Alice M. Graham, Eric Feczko, Oscar Miranda-Dominguez, Jerod M. Rasmussen, Rahel Nardos, Sonja Entringer, Pathik D. Wadhwa, Claudia Buss & Damien A. Fair in Nature Neuroscience. Published April 9 2018,
Maternal IL-6 during pregnancy can be estimated from newborn brain connectivity and predicts future working memory in offspring
Several lines of evidence support the link between maternal inflammation during pregnancy and increased likelihood of neurodevelopmental and psychiatric disorders in offspring. This longitudinal study seeks to advance understanding regarding implications of systemic maternal inflammation during pregnancy, indexed by plasma interleukin-6 (IL-6) concentrations, for large-scale brain system development and emerging executive function skills in offspring. We assessed maternal IL-6 during pregnancy, functional magnetic resonance imaging acquired in neonates, and working memory (an important component of executive function) at 2 years of age. Functional connectivity within and between multiple neonatal brain networks can be modeled to estimate maternal IL-6 concentrations during pregnancy. Brain regions heavily weighted in these models overlap substantially with those supporting working memory in a large meta-analysis. Maternal IL-6 also directly accounts for a portion of the variance of working memory at 2 years of age. Findings highlight the association of maternal inflammation during pregnancy with the developing functional architecture of the brain and emerging executive function.