Skip to main content
. Author manuscript; available in PMC: 2021 Mar 19.
Published in final edited form as: Reprod Toxicol. 2020 Mar 19;92:4–10. doi: 10.1016/j.reprotox.2020.03.006

Table 1.

Needs for Exposome Epidemiology

>Extension of environmental epidemiology to analysis of omics scale exposure data
>Improved environmental chemical and xenobiotic metabolite identification
>Improved quantification procedures for low abundance environmental chemicals
>Assembly of omics scale xenobiotics and metabolites data for pregnancy exposome of more than 10,000 individuals across multiple generations
>Coupling of exposome data to epigenetic data to develop systematic knowledge of the best characterized mechanism for exposure memory
>Maintenance of cohorts with coverage of critical developmental exposure windows and consequences for multiple subsequent generations to link ancestral developmental exposures to current health problems; Record exposures in real time, or link to resources to recorded exposures (e.g. newborn blood spots, stored prenatal sera) for multiple generations to comprehend E × E × G impacts on current populations
Expansion of high-resolution exposomics and metabolomics analyses
Initiation of pilot G × E and predictive modeling studies that result from exposomics studies
Integration of ‘omics within informative populations—tracing G × E revealed by the metabolome to track the epigenome, genome, proteome, transcriptome effects—use for pilot testing of approaches for mitigation