Salivary metabolomics in the family environment: A large-scale study investigating oral metabolomes in children and their parental caregivers
Rothman, J. A.; Piccerillo, H. L.; Riis, J. L.; Granger, D. A.; Thomas, E. A.; Whiteson, K. L.
Show abstract
Human metabolism is complex and dynamic, and is impacted by genetics, diet, health, and countless inputs from the environment. Beyond the genetics shared by family members, cohabitation leads to shared microbial and environmental exposures. Furthermore, metabolism is affected by factors such as inflammation, environmental tobacco smoke (ETS) exposure, metabolic regulation, and exposure to heavy metals. Metabolomics represents a useful analytical method to assay the metabolism of individuals to find potential biomarkers for metabolic conditions that may not be phenotypically obvious or represent unknown physiological processes. As such, we applied untargeted LC-MS metabolomics to archived saliva samples from a racially diverse group of elementary school-aged children and their caregivers collected during the "90-month" assessment of the Family Life Project. We assayed a total of 1,425 saliva samples of which 1,344 were paired into 672 caregiver/child dyads. We compared the metabolomes of children (N = 719) and caregivers (N = 706) within and between homes, performed population-wide "metabotype" analyses, and measured associations between metabolites and salivary biomeasures of inflammation, antioxidant potential, ETS exposure, metabolic regulation, and heavy metals. Dyadic analyses revealed that children and their caregivers have largely similar salivary metabolomes. Although there were differences between the dyads at the individual levels of analysis, dyad explained most (62%) of the metabolome variation. At a population level of analysis, our data clustered into two large groups, indicating that people likely share most of their metabolomes, but that there are distinct "metabotypes" across large sample sets. Lastly, individual differences in several metabolites - which were putative oxidative damage-associated or pathological markers - were significantly correlated with salivary measures indexing inflammation, antioxidant potential, ETS exposure, metabolic regulation, and heavy metals. Implications of the effects of family environment on metabolomic variation at the population, dyadic, and individual levels of analyses for health and human development are discussed.
Matching journals
The top 12 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- The association between salivary amylase gene copy number and enzyme activity with type 2 diabetes status 93%
- Cross-tissue comparison of telomere length and quality metrics of DNA among individuals aged 8 to 70 years 92%
- Arsenic exposure is associated with elevated sweat chloride concentration and airflow obstruction among adults in Bangladesh: a cross sectional study 91%
Similar papers in this journal
- Early life infection and proinflammatory, atherogenic metabolomic and lipidomic profiles at 12 months of age: a population-based cohort study 93%
- Environment-wide and epigenome-wide association study of adiposity in "Children of 1997" birth cohort 92%
- Ontogeny of plasma lipid metabolism in pregnancy and early childhood: a longitudinal population study 92%
Similar papers in this journal
- Systems analysis of gut microbiome influence on metabolic disease in HIV and high-risk populations 94%
- Metabolome-informed microbiome analysis refines metadata classifications and reveals unexpected medication transfer in captive cheetahs 92%
- Spatial metabolomics reveals localized impact of influenza virus infection on the lung tissue metabolome 92%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.