Maternal Metabolomic Profile and Fetal Programming of Offspring Adiposity: Identification of Potentially Protective Lipid Metabolites
Year: 2018
Type: article
Study design: Observational Study
Abstract: SCOPE: The fetal programming paradigm posits that the origins of obesity can be traced, in part, to the intrauterine period of life. However, the mechanisms underlying fetal programming are not well understood, and few studies have measured offspring adiposity in the neonatal period. The aim of this study is to identify maternal metabolites, and their determinants, that are associated with neonatal adiposity. METHODS AND RESULTS: A targeted metabolomics approach is applied to analyze plasma samples collected across gestation from a well-characterized cohort of 253 pregnant women participating in a prospective study at the University of California, Irvine. Whole-body dual X-ray absorptiometry (DXA) imaging of body composition is obtained in N = 121 newborns. Statistical models are adjusted for potential confounders and multiple testing. The authors identify six alkyl-linked phosphatidylcholines (PCae), containing fatty acid 20:4, that are significantly and negatively associated with neonatal body fat percentage. Factors indicating higher socioeconomic status, non-Hispanic ethnicity, and higher nonesterified fatty acid percentages are positively associated with these PCae. CONCLUSIONS: The polyunsaturated fatty acid 20:4 contained in PCae may exert a beneficial effect with respect to future propensity for obesity development. Prepregnancy and early pregnancy factors are determinants of these PCae, highlighting the importance of addressing preconceptional conditions for fetal programming of newborn adiposity.
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: National Institutes of Health, University of California, Irvine, Horizon 2020 Framework Programme, Seventh Framework Programme, National Institute of Mental Health, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development, H2020 European Research Council
Awards: Prenatal stress biology, infant body composition and obesity risk, G2864033895, G2877313677, Institute for Clinical and Translational Science, G3980639681, FETAL PROGRAMMING OF THE NEWBORN AND INFANT HUMAN BRAIN, G5372197592, EMA Assessment of Biobehavioral Processes in Human Pregnancy, Prenatal diet-stress interactions and the maternal metabolic response in human pregnancy
OpenAlex ID: W2802360262
