Developmental Core A major challenge to children's environmental health research is capturing the dynamic nature of environment, particularly how to capture it retrospectively. The lack of advanced exposure tools to address exposure timing limits research on critical windows of susceptibility ? life stages when individuals are highly vulnerable to environmental exposures. Prospective birth cohorts may capture these relationships, but are expensive both in time and money. The absence of objective retrospective biomarkers that provide information on both the magnitude and timing of fetal and early childhood exposure to multiple chemicals is a major barrier in environmental epidemiology. The primary mission of the Developmental Core is to develop, validate and standardize precise, unbiased, retrospective biomarkers of multi-chemical exposures at specific life stages including prenatal life, effectively providing data equivalent to a prospective longitudinal design. A major focus will be retrospective exposure reconstruction biomarkers that objectively measure prenatal and infant environment, even when samples are collected during childhood or adolescence. These will include tooth matrix-based biomarkers that exploit dentine growth rings to reconstruct the timing and dose of toxic/nutrient elements and organic chemical exposures in fetal life and infancy. We will also develop dental matrix based untargeted assays to create a `retrospective dynamic exposome' biomarker. In parallel, we will also develop methods to estimate embryonic and early fetal exposure using innovative assays of hair collected from pregnant women to reconstruct temporal periconceptual chemical exposures. It is now recognized that tissue architecture must be considered during any chemical analyses for exposure assessment. Our Core will apply multidimensional (2D and 3D) tissue bio-imaging that quantifies the spatial distribution of both metals and biomolecules within tissue sections using high-resolution laser-based mass spectrometry combined with multiplexed metal-tagged immunolabelling. We will also develop metalloproteomic techniques that can investigate metal-toxin metabolism and its effects on normal metal homeostasis. Finally, the Core Co-Leader (Baccarelli) is a renowned expert in environmental epigenetics and will develop novel biological response biomarkers that address the DNA conformational states that arise from DNA methylation and histone modifications. He will also work jointly with Core Leader (Arora) on measuring miRNA and mtDNA biomarkers in hair that can recapitulate past biological response to the environment, thereby complementing Dr. Arora's work on laser ablation ICP-MS and hair metals. The Developmental Core will integrate with the other Resources, so that our work can be incorporated as services offered by the three Hub Resources. This will be accomplished through shared personnel, resources and the monthly Executive Steering Committee meetings. Our goal is to bring new biomarkers into the CHEAR network as fully developed, high-throughput platforms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Resource-Related Research Multi-Component Projects and Centers Cooperative Agreements (U2C)
Project #
1U2CES026561-01
Application #
9062194
Study Section
Special Emphasis Panel (ZES1-LWJ-J (UC))
Project Start
2015-09-30
Project End
2019-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
1
Fiscal Year
2015
Total Cost
$1,040,000
Indirect Cost
$269,938
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Wright, Robert O; Teitelbaum, Susan; Thompson, Claudia et al. (2018) The child health exposure analysis resource as a vehicle to measure environment in the environmental influences on child health outcomes program. Curr Opin Pediatr 30:285-291
Sanders, Alison P; Saland, Jeffrey M; Wright, Robert O et al. (2018) Perinatal and childhood exposure to environmental chemicals and blood pressure in children: a review of literature 2007-2017. Pediatr Res 84:165-180
Curtin, Paul; Austin, Christine; Curtin, Austen et al. (2018) Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder. Sci Adv 4:eaat1293
Smith, Tanya M; Austin, Christine; Hinde, Katie et al. (2017) Cyclical nursing patterns in wild orangutans. Sci Adv 3:e1601517
Wright, Robert O (2017) Environment, susceptibility windows, development, and child health. Curr Opin Pediatr 29:211-217
Andra, Syam S; Austin, Christine; Patel, Dhavalkumar et al. (2017) Trends in the application of high-resolution mass spectrometry for human biomonitoring: An analytical primer to studying the environmental chemical space of the human exposome. Environ Int 100:32-61
Wolff, Mary S; Buckley, Jessie P; Engel, Stephanie M et al. (2017) Emerging exposures of developmental toxicants. Curr Opin Pediatr 29:218-224
Evrard, Solene M; Lecce, Laura; Michelis, Katherine C et al. (2016) Endothelial to mesenchymal transition is common in atherosclerotic lesions and is associated with plaque instability. Nat Commun 7:11853
Kappil, Maya; Wright, Robert O; Sanders, Alison P (2016) Developmental Origins of Common Disease: Epigenetic Contributions to Obesity. Annu Rev Genomics Hum Genet 17:177-92
Andra, Syam S; Austin, Christine; Yang, Juan et al. (2016) Recent advances in simultaneous analysis of bisphenol A and its conjugates in human matrices: Exposure biomarker perspectives. Sci Total Environ 572:770-781

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