Gestational age-dependent development of the neonatal metabolome

Ernst, M. et al. (2021) Gestational age-dependent development of the neonatal metabolome. Pediatric Research, 89(6), pp. 1396-1404. (doi: 10.1038/s41390-020-01149-z) (PMID:32942288)

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Abstract

Background: Prematurity is a severe pathophysiological condition, however, little is known about the gestational age-dependent development of the neonatal metabolome. Methods: Using an untargeted liquid chromatography-tandem mass spectrometry metabolomics protocol, we measured over 9000 metabolites in 298 neonatal residual heel prick dried blood spots retrieved from the Danish Neonatal Screening Biobank. By combining multiple state-of-the-art metabolome mining tools, we retrieved chemical structural information at a broad level for over 5000 (60%) metabolites and assessed their relation to gestational age. Results: A total of 1459 (~16%) metabolites were significantly correlated with gestational age (false discovery rate-adjusted P < 0.05), whereas 83 metabolites explained on average 48% of the variance in gestational age. Using a custom algorithm based on hypergeometric testing, we identified compound classes (617 metabolites) overrepresented with metabolites correlating with gestational age (P < 0.05). Metabolites significantly related to gestational age included bile acids, carnitines, polyamines, amino acid-derived compounds, nucleotides, phosphatidylcholines and dipeptides, as well as treatment-related metabolites, such as antibiotics and caffeine. Conclusions: Our findings elucidate the gestational age-dependent development of the neonatal blood metabolome and suggest that the application of metabolomics tools has great potential to reveal novel biochemical underpinnings of disease and improve our understanding of complex pathophysiological mechanisms underlying prematurity-associated disorders. Impact: A large variation in the neonatal dried blood spot metabolome from residual heel pricks stored at the Danish Neonatal Screening Biobank can be explained by gestational age. While previous studies have assessed the relation of selected metabolic markers to gestational age, this study assesses metabolome-wide changes related to prematurity. Using a combination of recently developed metabolome mining tools, we assess the relation of over 9000 metabolic features to gestational age. The ability to assess metabolome-wide changes related to prematurity in neonates could pave the way to finding novel biochemical underpinnings of health complications related to preterm birth.

Item Type:Articles
Additional Information:This research has been conducted using the Danish National Biobank resource, and supported by the Novo Nordisk Foundation. The study was sponsored by the Lundbeck Foundation, grant numbers R102-A9118 and R155-2014-1724.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Rogers, Dr Simon
Authors: Ernst, M., Rogers, S., Lausten-Thomsen, U., Björkbom, A., Laursen, S. S., Courraud, J., Børglum, A., Nordentoft, M., Werge, T., Mortensen, P. B., Hougaard, D. M., and Cohen, A. S.
College/School:College of Science and Engineering > School of Computing Science
Journal Name:Pediatric Research
Publisher:Springer Nature
ISSN:0031-3998
ISSN (Online):1530-0447
Published Online:17 September 2020

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