The study, published in Nature Pediatric Research by scientists at the UCSF California Preterm Birth Initiative (PTBI-CA), assessed the records of 9,639 preterm infants who experienced mortality or at least one complication or mortality.

Using the results of standard newborn profiles and blood tests, they identified a combination of six newborn characteristics and 19 metabolites that, together, created a vulnerability profile that reliably identified preterm babies at substantially increased risk for death and severe illness.

"Our results point to a number of potential biological pathways that may play a key role in the development of negative outcomes in babies born preterm," said the study's lead author Scott Oltman, MS, epidemiologist, UCSF PTBI-CA. "If we can better understand these pathways, new treatments or preventative measures may be possible."

The study appears online in Nature Pediatric Research.

Metabolites are molecules such as glucose or thyroid stimulating hormone (TSH) that are naturally produced by our cells as we break down food or medications. In a newborn, these molecules may originate from the mother's bloodstream or be generated by the infant and can be used to assess whether the body is functioning normally.

Of particular note are the investigative team's findings that Black babies were 35 percent more likely than white babies to die or experience major complications, including serious breathing and digestive conditions known as respiratory distress syndrome and necrotizing enterocolitis.

"We are particularly excited about the potential for these metabolic models to help us address critical inequities in outcomes in Black infants," said senior author Laura Jelliffe-Pawlowski, PhD, MS, professor of Epidemiology and Biostatistics in the UCSF School of Medicine, and director of Discovery and Precision Health with PTBI-CA. "Going forward, we should be able to create personalized care plans for each baby born too early, which will help us reduce race/ethnic disparities in outcomes."

Advances in science have enabled even the most fragile preterm babies to survive in greater numbers and at younger gestational ages. In the United States, approximately 1 in 10 live infants is delivered preterm. However, preterm birth and related comorbidities are the leading cause of death for U.S. children under five years of age, with neonatal (newborn) deaths accounting for 46 percent of mortality in this age group.

Previous models attempting to predict complications after preterm birth have relied only upon the infant's gestational age, birthweight and other clinical characteristics. This study expanded the characteristics to include maternal factors, such as race, maternal age and education. It also identified 19 molecules such as TSH and glycine that also contributed to prediction. These metabolites are routinely tested in newborn screens, but are not assessed as a composite. These metabolites play important roles in many biological pathways including in digestion, respiration and temperature regulation.

"Some of the pathways we have identified may offer inroads for intervention and could eventually lead to fewer deaths and lessened short- and long-term disability in babies born too early," Jelliffe-Pawlowski said.

This study is paving the way for continued research on how these models could help preterm newborn babies. The next phase of this study is funded by the National Institutes of Health and begins this fall through 2025. It will enroll 100 very preterm babies in California and Iowa to test how well the newly identified metabolic models work in neonatal intensive care unit (NICU) settings. As part of this work, PTBI-CA researchers will collaborate with the Benioff Center for Microbiome Medicine to look at the microbiomes of babies in the new study to identify additional drivers of short- and long-term of outcomes.

Story Source:

Materials provided by University of California - San Francisco. Original written by Lorna Fernandes. Note: Content may be edited for style and length.

Journal Reference:

1. Scott P. Oltman, Elizabeth E. Rogers, Rebecca J. Baer, Elizabeth A. Jasper, James G. Anderson, Martina A. Steurer, Matthew S. Pantell, Mark A. Petersen, J. Colin Partridge, Deborah Karasek, Kharah M. Ross, Sky K. Feuer, Linda S. Franck, Larry Rand, John M. Dagle, Kelli K. Ryckman, Laura L. Jelliffe-Pawlowski. Newborn metabolic vulnerability profile identifies preterm infants at risk for mortality and morbidity. Pediatric Research, 2020; DOI: 10.1038/s41390-020-01148-0