Non-linear and non-additive associations between the pregnancy metabolome and birthweight
E Colicino1, F Ferrari2, W Cowell1
1Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Insights
Maternal serum metabolites during pregnancy, including lipids, are linked to newborn birthweight through linear, non-linear, and synergistic effects. This research highlights the complex interplay of the prenatal metabolome in fetal growth.
Area of Science:
- Metabolomics
- Perinatal Epidemiology
- Endocrinology
Background:
- Birthweight is a key indicator of fetal growth and health.
- Altered birthweight is associated with adult disorders.
- Previous studies overlooked maternal serum metabolome and complex exposure associations.
Purpose of the Study:
- Investigate maternal serum metabolome's association with birthweight for gestational age (BWGA) z-score.
- Explore linear, non-linear, and synergistic effects of metabolites.
- Identify key metabolites and their biological functions related to BWGA z-score.
Main Methods:
- Untargeted metabolomics on maternal serum from 410 mother-child dyads.
- Bayesian factor analysis for interaction to identify important metabolites and associations.
- Functional enrichment analysis using MetaboAnalyst.
Main Results:
- 46 out of 1110 metabolites showed U-shaped associations with BWGA z-score.
- Lipids were the predominant metabolites, involved in energy, immune, and hormone metabolism.
- Steroids and phospholipids exhibited synergistic interactions.
Conclusions:
- Maternal metabolome significantly influences newborn birthweight through various association types.
- Non-linear and synergistic effects of metabolites are crucial for understanding birthweight variation.
- Findings emphasize the role of prenatal metabolic environment in fetal development.
Background:
Birthweight is an indicator of fetal growth and environmental-related alterations of birthweight have been linked with multiple disorders and conditions progressing into adulthood. Although a few studies have assessed the association between birthweight and the totality of exogenous exposures and their downstream molecular responses in maternal urine and cord blood; no prior research has considered a) the maternal serum prenatal metabolome, which is enriched for hormones, and b) non-linear and synergistic associations among exposures.
Methods:
We measured the maternal serum metabolome during pregnancy using an untargeted metabolomics approach and birthweight for gestational age (BWGA) z-score in 410 mother-child dyads enrolled in the PRogramming of Intergenerational Stress Mechanisms (PRISM) cohort. We leveraged a Bayesian factor analysis for interaction to select the most important metabolites associated with BWGA z-score and to evaluate their linear, non-linear and non-additive associations. We also assessed the primary biological functions of the identified proteins using the MetaboAnalyst, a centralized repository of curated functional information. We compared our findings with those of a traditional metabolite-wide association study (MWAS) in which metabolites are individually associated with BWGA z-score.
Results:
Among 1110 metabolites, 46 showed evidence of U-shape associations with BWGA z-score. Most of the identified metabolites (85%) were lipids primarily enriched for pathways central to energy production, immune function, and androgen and estrogen metabolism, which are essential for pregnancy and parturition processes. Metabolites within the same class, i.e. steroids and phospholipids, showed synergistic relationships with each other.
Conclusions:
Our results support that the aspects of the maternal metabolome during pregnancy contribute linearly, non-linearly and synergistically to variation in newborn birthweight.
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